Journal of Diabetes Research

Journal of Diabetes Research / 2020 / Article

Research Article | Open Access

Volume 2020 |Article ID 2817972 | https://doi.org/10.1155/2020/2817972

Xiao Meng Zhang, Hao Deng, Jin Dong Tong, Yi Zhen Wang, Xu Chao Ning, Xiu Hong Yang, Fang Qiang Zhou, Hui Min Jin, "Pyruvate-Enriched Oral Rehydration Solution Improves Glucometabolic Disorders in the Kidneys of Diabetic db/db Mice", Journal of Diabetes Research, vol. 2020, Article ID 2817972, 13 pages, 2020. https://doi.org/10.1155/2020/2817972

Pyruvate-Enriched Oral Rehydration Solution Improves Glucometabolic Disorders in the Kidneys of Diabetic db/db Mice

Academic Editor: Ilaria Campesi
Received08 Apr 2020
Revised14 Aug 2020
Accepted27 Aug 2020
Published25 Sep 2020

Abstract

Diabetes is prevalent worldwide, but ideally intensive therapeutic strategy in clinical diabetes and diabetic nephropathy (DN) is still lack. Pyruvate is protective from glucometabolic disturbances and kidney dysfunction in various pathogenic insults. Present studies focused on oral pyruvate effects on diabetes status and DN with 0.35% pyruvate in pyruvate-enriched oral rehydration solution (Pyr-ORS) and 1% pyruvate as drinking water for 8 weeks, using the model of diabetic db/db mice. Both Pyr-ORS and 1% pyruvate showed comparable therapeutic effectiveness with controls of body weight and blood sugar, increases of blood insulin levels, and improvement of renal function and pathological changes. Aberrant key enzyme activities in glucometabolic pathways, AR, PK, and PDK/PDH, were also restored; indexes of oxidative stress and inflammation, NAD+/NADH ratio, and AGEs in the kidneys were mostly significantly preserved after pyruvate treatments. We concluded that oral pyruvate delayed DN progression in db/db mice and the modified Pyr-ORS formula might be an ideal novel therapeutic drink in clinical prevention and treatment of type 2 diabetes and DN.

1. Introduction

Diabetes has become one of the most severe chronic diseases worldwide. According to 2017 statistics, diabetes mellitus (DM) patients are about 425 million in the world, which is about three times the number of diabetic patients in 2000 [1]. Diabetic nephropathy (DN) develops in over 30% of diabetic patients and is the leading cause of chronic kidney disease and end-stage renal disease with a high mortality in westernized countries [2].

Accumulating studies demonstrated that disturbances of glucose metabolic pathways, particularly, pyruvate kinase (PK M2) depression and the Warburg phenomenon, glomerular microvascular endothelial mitochondrial dysfunction, and endoplasmic reticulum stress in renal proximal tubular epithelial cells all stimulated by hyperglycemia (HG) play crucial roles in DN onset and progression in diabetic rodent models and patients [37]. Specifically, renal hypoxia, oxidative stress, inflammation, and advanced glycation end products (AGEs) are simultaneously participated in the process, leading to a vicious circle in DN exacerbation [710]. However, underlying molecular and metabolic mechanisms of DN initiation and progression are still not fully illustrated.

Numerous studies convincingly demonstrated that pyruvate was protective of glucose metabolism in various pathogenic insults [1118]. Since 1990s, studies have shown that pyruvate displays the valuable protection against cellular aberrant glucometabolic pathways and redox status in HG status and diabetic cataract and retinopathy in animals and human cells [11, 12]. It has been revealed that pyruvate holds unique pleiotropic biological and pharmacological properties: increase of hypoxia tolerance, correction of glucometabolic disturbances and acid-base unbalance, action of antioxidative stress/inflammation, protection of mitochondria, and inhibition of cellular apoptosis [1315]. Therefore, pyruvate robustly preserves multiorgan function, of which the kidney protection from oxidative stress, hypoxia/ischemia reperfusion, and poisoning injuries has been explicitly illustrated [1618]. Further, oral 1-3% pyruvate apparently improved diabetic cataract and retinopathy, and pyruvate has been known to prevent or attenuate as well as delay AGE formation in rodent diabetic cataract lens [19, 20]. However, ingestion of pure pyruvate products does not benefit in humans (see below). In this terms, oral or enteral pyruvate (0.35%) in pyruvate-enriched, sodium-, glucose-containing oral rehydration solution (Pyr-ORS) has recently shown unequivocally beneficial in organ metabolism and function, including kidney, and significantly increases survival, relative to World Health Organization-guided ORS (WHO-ORS), in animals subjected to severe injuries [21, 22].

On this basis, the present study was undertaken to focus on effects of pyruvate-enriched fluid, i.e., Pyr-ORS (containing 0.35% pyruvate and 1.35% glucose) and pure 1% pyruvate as drinking water on type 2 diabetes, mainly DN, in diabetic db/db mice. As a preliminary descriptive study, results hereby ascertain that oral pyruvate is powerfully beneficial in diabetic db/db mice and first provide a possibility of the novel strategy with Pyr-ORS to improve glucometabolic profile in prevention and treatment of clinical type 2 diabetes and its organ complications including DN in a large population.

2. Materials and Methods

The experiment was conducted in compliance with the Guide for Care and Use of Laboratory Animals of the National Research Council of China, Beijing, China. All experimental protocols were reviewed and approved by the Ethics Committee of the Pudong Hospital, Shanghai Medical School, Fudan University, Shanghai, China.

2.1. Animal and Experimental Grouping

C57BLKS/J mice and diabetes mellitus (DM) C57BL/6 db/db mice (male, 6 weeks old) were purchased from Nanjing Biomedical Research Institute, Nanjing, China, and housed in plastic cages with a controlled temperature of 23-26°C, humidity of 50-55%, and a 12 h light/dark cycle in the specific pathogen free room (4 mice per cage). After acclimatized for 4 weeks, the DM C57BL/6 db/db mice were confirmed by the symptoms of hyperglycemia, polyphagia, polydipsia, and polyuria. Only those animals with fasting plasma glucose higher than 11.1 mmol/l (blood drawn from tail vein; glucose tested by Roche blood glucose meter) were selected as the diabetic model for the following experiments. A total of 24 animals at the age of 10 weeks old, including 6 C57BLKS/J normal nontreated mice as the normal group (group Nor), were selected, and 18 db/db DM mice were randomly divided into three groups with 6 mice in each. The control group (group Con) was DM nontreated mice. The pyruvate group (group Pyr) was DM mice drunk distilled water containing 1% sodium pyruvate (NaPyr), while the Pyr-ORS group (group Pyr-ORS) was DM mice given distilled water containing 0.35% NaPyr in oral rehydration salts (ORS). Groups Nor and Cor regularly fed experimental water. All the mice in four groups had free access to normal experimental diet with fluids mentioned above, respectively. The water consumption was above 10 ml/day by the weight of the water bottle each mouse. Body and kidney weights, fasting blood glucose and insulin concentrations, and 24-hour volume urine in a metabolic cage were collected and measured at the ages of 10 and 18 weeks old each mouse.

After 8 weeks, at the age of 18 weeks old, all animals were euthanized by an i.p. injection of pentobarbital sodium (200 mg/kg), and 1.3 ml of blood samples were collected by cardiac puncture each mouse, then centrifuged at 4000 r/min for 10 minutes to separate plasma, which were frozen at -80°C. The kidney was quickly removed from each mouse and frozen at -80°C. Pyr-ORS was fleshly prepared in the laboratory with 0.35% NaPyr, 0.2% NaCl, 0.15% Kcl, and 1.35% glucose anhydrate with 247 mOsm/l [23]. Sodium pyruvate was obtained from Thermo Fisher (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA).

2.2. Enzyme-Linked Immunosorbent Assay (ELISA)

Mouse kidney homogenates were individually prepared for detecting the levels of pyruvate dehydrogenase (PDH), including nonphosphorylated active pyruvate dehydrogenase (PDHa), total pyruvate dehydrogenase (PDHt) and pyruvate kinase (PK) (Yili Biology Technology, Shanghai, China); oxidized/reduced nicotinamide adenine dinucleotides (NAD+/NADH), Cystatin C (Cys-C), and AGEs (Jiancheng Bioengineering Institute, Nanjing, China); and insulin, lactate dehydrogenase (LDH), and radical oxygen species (ROS) (Yili Biology Technology, Shanghai, China), using respective ELISA kit following protocols. The levels of serum creatinine (Cr) and BUN and superoxide dismutase (SOD), catalase (CAT), malondialdehyde (MDA), glutathione peroxidase (GSH-PX), fructose, and sorbitol in kidney homogenates were detected; 24-hour urinary protein and neutrophil gelatinase-associated lipocalin (NGAL) were also measured with respective commercial assay kits (Nanjing Jiancheng, Nanjing, China).

The detection method of ROS was briefly as follows: diluted the sample and placed it in the plate, by adding the enzyme-labeled antibody, then the substrate solution for the color reaction, and finally, terminated the reaction by adding the stop solution. The OD value was measured with an enzyme mark instrument (infinite m200pro TECAN, Switzerland). The NAD+/NADH detection was briefly that tissues were lysed and heated with acidic/alkalic extracts to obtain NAD+ and NADH, then mixed with respective reagents and incubated at 80°C for 60 min in protection from light. The OD value was measured at a wavelength of 570 nm. The ratio was obtained through a specific calculation formula provided by the assay kit.

2.3. Western Blotting

The proteins used for Western blotting were extracted using lysis buffer (Inventbiotechnologies, INC, China), separated by the sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), and transferred onto polyvinylidene difluoride (PVDF) membrane (Millipore, Bedford, MA, USA). The membrane carrying protein bands was blocked in Tris-buffered saline with Tween (TBST) with 5% skim milk for 1 h and incubated with primary antibodies (Proteintech Group, Inc., IL, USA) at 4°C overnight. After washing, the membrane was incubated with secondary antibodies marked by horseradish peroxidase for 1 h at room temperature. Secondary antibodies (Proteintech Group, Inc., IL, USA) included goat anti-rabbit IgG and goat anti-mouse IgG. After washing, the membrane carrying blots and antibodies was incubated with Immobilon Western Chemiluminescent HRP Substrate (Millipore). Signals of proteins were captured, using a Bio-Rad ChemiDoc™ XRS system (Bio-Rad, Hercules, CA, USA). Data were quantified by the Quantity One software (Bio-Rad). Primary antibodies against aldose reductase (AR) were purchased from GeneTex (CA, USA); those against PDH, PDHA1, and pyruvate dehydrogenase kinas (PDK) were purchased from Cell Signaling Technology (CST, Beverly, MA, USA); antibodies against PDK and PDHA1 were obtained from Abways Technology (Abways Technology Inc, Shanghai, China).

2.4. Immunohistochemistry Analysis

For the immunohistochemistry procedure for renal PDH, paraffin-embedded sections were prepared, dewaxed, and repaired using ethylenediaminetetraacetic acid (EDTA) antigen retrieval buffers. Next, the sections were incubated with the antibody (CST, Beverly, MA, USA) against PDH in PBS containing 3% bovine serum albumin (BSA) overnight at 4°C. The samples were then incubated with the secondary antibody (CST, Beverly, MA, USA) for 45 minutes at room temperature. Then, sections were stained using a 3,3-diaminobenzidine (DAB) procedure, and the nucleus were restained using hematoxylin. Finally, the sections were mounted on slides for image analysis. The percentage of positive staining area was quantified, using Image-Pro Plus 6.0 software (Media Cybernetics, Silver Spring, MD, USA). The expression of protein was detected by mean density.

2.5. PAS Staining and Transmission Electron Microscopy

Kidney tissue histopathological examination by the light microscopy with the Periodic Acid-Schiff (PAS) staining was following regular experimental procedures: briefly, slices were deparaffinized and hydrate to water, immersed in 0.5% periodic acid for 15 min, in Schiff’s reagent for 30 min, and then in Mayer’s haematoxylin solution for 3 min followed by washing in water every step. Finally, after blued up with ammonia solution, slices were used with alcohol and xylene to dehydrate and mount.

Evaluation of kidney injuries was by glomerular sclerosis index and tubulointerstitial injury index. Imaging analysis in PAS staining was carried out as follows: obtained the total area of the glomerulus by checking the enlarged image and then the mesangial area (excluding basement membrane and other parts). The mesangial area index was calculated from the ratio of the mesangial area to the glomerular area expressed by % and quantified by using Image-Pro Plus 6.0 software (Media Cybernetics, Silver Spring, MD, USA). Mesangial matrix index (%) was independently evaluated by three pathologists to assess glomerular damage in an average. The average percentage of mean density area (IOD/area) was quantified using Image-Pro Plus 6.0 software (Media Cybernetics, Silver Spring, MD, USA). Tubular injury was not investigated. For the transmission electron microscopy (TEM) procedure, fresh tissue blocks were isolated by preventing from physical damage with the size of tissue block no more than 1 mm3. The tissue blocks were then followed by regular experimental procedures and then cut into ultrathin sections (60-80 nm) with an ultramicrotome. Finally, sections were observed with TEM (Hitachi HT770, Japan). The injured areas were marked by arrows.

2.6. Statistical Analysis

All experiments were repeated three times, and data were presented as the (SEM). Statistical analyses were performed using SPSS 22.0 statistical software (SPSS, Chicago, IL, USA). A one-way analysis of variance (ANOVA) was used to calculate the values, and was considered statistically significant.

3. Result

3.1. Changes in Body Weight (BW), Kidney Weight/Body Weight (KW/BW) and Levels of Fasting Plasma Glucose and Insulin

After oral pyruvate treatments (1% pyruvate or Pyr-ORS) for 8 weeks (Table 1), the BW of all db/db mice was still higher than that of all normal mice, but was significantly lower () in groups Pyr and Pyr-ORS compared with group Con; the KW/BW ratio was higher in group Pyr than that in group Pyr-ORS relative to group Con (), indicating that 1.0% pyruvate was more beneficial than 0.35% pyruvate of Pyr-ORS in the BW decrease in diabetic db/db mice. Compared with group Con, fasting blood glucose levels were decreased (), whereas levels of fasting plasma insulin were significantly increased () in groups Pyr and Pyr-ORS () after the treatment. Results indicated that oral pyruvate in two pyruvate groups almost comparably improved diabetes status in db/db mice.


NorConPyrPyr-ORS

BW (g)
 Week 0####
 Week 8####
KW/BW (mg/g)
 Week 0
 Week 8##
Glucose (mmol/l)
 Week 0
 Week 8##
Insulin (ng/ml)
 Week 0
 Week 8####

Nor (normal), C57BLKS/J nontreated mice; Con (control), C57BLKS/J diabetic db/db nontreated mice; Pyr, db/db mice drunk distilled water containing 1% pyruvate; Pyr-ORS, db/db mice drunk pyruvate-enriched ORS to replace distilled water, containing 0.35% pyruvate; BW: body weight; KW/BW: kidney weight/body weight; glucose: fasting plasma glucose; insulin: fasting plasma insulin; and vs. Nor; # and ## vs. Con. Values were at week 0 and at week 8, respectively.
3.2. Changes in Serum Cr, BUN, and Cys-C and Levels of Urine Protein and NGAL

In Table 2, compared with group Nor, serum Cr, BUN, and Cys-C, urine NGAL, and 24-hour urinary protein were significantly higher in all db/db mice; however, the indicators of early sensitive kidney function, serum Cys-C and urine NGAL, were significantly lower () in groups Pyr and Pyr-ORS after 8 weeks of treatments. In group Pyr, 24-hour urinary protein was also remarkably lower (). In terms of serum Cr and BUN, the pyruvate effect was not obvious in the experiment. Data suggested that oral pyruvate in two pyruvate groups comparably protected kidney function against diabetes and delayed DN exacerbation in db/db mice.


NorConPyrPyr-ORS

Serum creatinine (mg/dl)
 Week 0
 Week 8#
Serum BUN (mg/dl)
 Week 0
 Week 8
Serum Cystatin C (ng/ml)
 Week 0
 Week 8##
Urine NGAL (ng/24 h)
 Week 0
 Week 8####
24-hour urinary protein (mg)
 Week 0
 Week 8#

Nor (normal), C57BLKS/J nontreated mice; Con (control), C57BLKS/J diabetic db/db nontreated mice; Pyr, db/db mice drunk distilled water containing 1% pyruvate; Pyr-ORS, db/db mice drunk pyruvate-enriched ORS to replace distilled water, containing 0.35% pyruvate; BUN: blood urea nitrogen; NAGL: neutrophil gelatinase-associated lipocalin. and vs. Nor; # and ## vs. Con. Values were at week 0 and at week 8, respectively.
3.3. Changes in Activities of Pyruvate Kinase, LDH, and PDHa/PDHt in Kidney Homogenates

As shown in Table 3, compared to group Con, there were significant alterations (higher or lower) in levels of LDH, PK, and PDHa/PDHt in the kidneys of groups Pyr and Pyr-ORS after the treatments ( or ). Particularly, HG-promoted LDH and HG-inhibited PDHa were mostly recovered. These data strongly showed that oral pyruvate in two pyruvate groups profoundly and comparably improved the key enzymes in glycolysis and glucose oxidative metabolism in diabetic db/db mice.


NorConPyrPyr-ORS

LDH (mU/mg protein)
 Week 0
 Week 8####
PK (mU/mg protein)
 Week 0
 Week 8###
PDHa/PDHt ratio
 Week 0
 Week 8##

Nor (normal), C57BLKS/J nontreated mice; Con (control), C57BLKS/J diabetic db/db nontreated mice; Pyr, db/db mice drunk distilled water containing 1% pyruvate; Pyr-ORS, db/db mice drunk pyruvate-enriched ORS to replace distilled water, containing 0.35% pyruvate; LDH: lactate dehydrogenase; PK: pyruvate kinase; PDHa/PDHt: activities of pyruvate dehydrogenase/total pyruvate dehydrogenase. and vs. Nor; # and ## vs. Con. Values were at week 0 and at week 8, respectively.
3.4. Changes in Sorbitol, Fructose, NAD+/NADH Ratio, and AGEs in Kidney Homogenates

As shown in Table 4, compared to group Con, sorbitol, fructose, NAD+/NADH ratio, and AGEs in kidney homogenates were markedly altered (higher or lower) in groups Pyr and Pyr-ORS, although sorbitol and fructose were not significantly reduced from statistical study in group Pyr-ORS, after treatments ( or ). Results revealed that oral pyruvate in two pyruvate groups significantly and comparably raised NAD+/NADH ratio and ameliorated AGEs formation in kidneys of diabetic db/db mice.


NorConPyrPyr-ORS

Sorbitol (mmol/mg protein)
 Week 0
 Week 8#
Fructose (mmol/mg protein)
 Week 0
 Week 8##
NAD+/NADH ratio
 Week 0
 Week 8####
AGEs (U/mg protein)
 Week 0
 Week 8####

Nor (normal), C57BLKS/J nontreated mice; Con (control), C57BLKS/J diabetic db/db nontreated mice; Pyr, db/db mice drunk distilled water containing 1% pyruvate; Pyr-ORS, db/db mice drunk pyruvate-enriched ORS to replace distilled water, containing 0.35% pyruvate; AGEs: advanced glycation end products; NAD+/NADH: nicotinamide adenine dinucleotide (oxidized form/reduced form). and vs. Nor; # and ## vs. Con. Values were at week 0 and at week 8, respectively.
3.5. Changes in the Expressions of Key Enzyme in Glucometabolic Pathways in Kidney Homogenates

Figure 1 showed the higher expressions of AR and PDK, but the lower expressions of PDH and PDHA1 (active form of PDH) induced by HG in kidney homogenates in group Con than in group Nor. However, all alterations were reversed after intervention with oral pyruvate in two pyruvate groups. These results strongly suggested that oral pyruvate recovered aberrant sorbitol pathway and reactivated glucose oxidative metabolism, resulting in renoprotection, in diabetic db/db mice.

3.6. Changes in Indexes of Oxidative Stress and Inflammation in Kidney Homogenates

Compared to group Con in Table 5, there were significant changes (higher or lower) in serum ROS, SOD, MDA, CAT, and GSH-PX levels in the kidneys of groups Pyr and Pyr-ORS after the 8-week study period ( or ). In Figure 2, there was a significant decrease in inflammatory factors (IL-1β, IL-6, and TNF-α) in the kidneys of group Pyr and a slight decrease in group Pyr-ORS after 8 weeks of pyruvate treatments. These data indicated that oral 1.0% or 0.35% pyruvate markedly attenuated oxidative stress: increased SOD, CAT, and GSH-Px, whereas decreased ROS and MDA, with a little inhibition of inflammation in kidneys of diabetic db/db mice.


NorConPyrPyr-ORS

ROS (IU/mg protein)
 Week 0
 Week 8##
SOD (U/mg protein)
 Week 0
 Week 8###
CAT (U/mg protein)
 Week 0
 Week 8###
MDA (μmol/mg protein)
 Week 0
 Week 8#
GSH-PX (μg/g protein)
 Week 0
 Week 8###

Nor (normal), C57BLKS/J nontreated mice; Con (control), C57BLKS/J diabetic db/db nontreated mice; Pyr, db/db mice drunk distilled water containing 1% pyruvate; Pyr-ORS, db/db mice drunk pyruvate-enriched ORS to replace distilled water, containing 0.35% pyruvate; ROS: radical oxygen species; SOD: superoxide dismutase; CAT: catalase; MDA: malondialdehyde. and vs. Nor; # and ## vs. Con. Values were at week 0 and at week 8, respectively.
3.7. Pyruvate Ameliorated Renal Histopathological Damage

The renoprotective effects of oral pyruvate in ameliorating renal morphological damage were investigated by PAS staining and transmission electron microscope. Immunohistochemistry studies showed that the protein expression levels of PDH by the mean density of integrated optical density (IOD/area) was seriously reduced in group Con, but equally and fully restored in groups Pyr and Pyr-ORS (Figures 3(a) and 3(e)). In Figure 3(b), the pathological changes of kidney tissues in PAS staining were eliminated in groups Pyr and Pyr-ORS in relation to group Con. Compared to the normal mice, there was a higher glomerular volume and mesangial matrix expansion in group Con, but oral pyruvate treatments parallelly attenuated mesangial matrix index and edema of glomerular endothelial cells and podocytes (see arrows in Figure 3(c)) in the kidney microstructure of groups Pyr and Pyr-ORS (Figures 3(b)–3(d)). Results from kidney morphological alterations indicated that oral pyruvate in two pyruvate groups comparably eliminated injuries of kidney histopathology in diabetic db/db mice.

4. Discussion

4.1. Pyruvate Delayed Progression of Diabetes Status and Diabetic Kidney Disease

Present results illustrated that oral pyruvate fluids as drinking water enabled to improve diabetes and attenuate DN progression in diabetic db/db mice, a widely acceptable standard model for type 2 diabetic patients. As shown in Tables 1 and 2, pyruvate in both 1% drinking water and Pyr-ORS (0.35% pyruvate) decreased the BW and fasting blood sugar and increased fasting blood insulin in like manner in two pyruvate groups after an 8-week treatment. Oral pyruvate (1% pyruvate or Pyr-ORS) in both groups significantly improved diabetic kidney function as preserved lower levels of blood Cys-C, 24-hour urine protein, and NGAL; further, kidney injuries in mesangial matrix and podocytes (Figures 3(b) and 3(c)) in histopathological alterations were diminished after pyruvate treatments for 8 weeks, compared to group Con. These results demonstrated that oral pyruvate fluids were effective in the treatment of diabetes and DN of db/db mice.

Glucometabolic data showed key enzymes: AR in sorbitol pathway, PK in glycolysis, and PDH in glucose oxidative metabolism were profoundly improved (Figures 1(b) and 3(a) and Table 3); oxidative stress and inflammation were reduced by oral pyruvate though inflammatory inhibition was minor in diabetic kidneys of db/db mice (Table 5 and Figure 2). Importantly, AGE levels in diabetic kidney were attenuated after oral pyruvate treatment for 8 weeks (Table 4). All findings supported that two oral pyruvate fluids analogously improved diabetic status and delayed DN progression in diabetic db/db mice. Notably, prior studies demonstrated that pyruvate improved diabetic ocular complications and discovered that pyruvate inhibited zinc-induced pancreatic islet cell death, and pyruvate supplementation attenuated β-cell death in vitro and in vivo experiments [11, 13, 24, 25]. However, to date, there has been no investigation concerning pyruvate effects on DN. Intriguingly, a preliminary clinical report revealed that a large dose of oral pyruvate (about 1.0 g/kg/d for 7-10 days) apparently controlled diabetes in 6 patients subjected to type 1 diabetes with a tendency of hypoglycaemia. An additional finding showed that oral pyruvate in a large dose improved the insulin secretion of β-cells in a mitochondrial DM patient with a reduction of total daily insulin dose [26, 27]. These case reports apparently support the present findings. The diabetic db/db mice model used in experiments is basically reflected with diabetic disorders in patients subjected to type 2 diabetes; the promising results here, which consisted with previous experimental findings and the case reports, provided a greater possibility for oral pyruvate to prevent and treat clinical diabetes.

4.2. Pyruvate Improved Glucometabolic Disturbances

The following novel findings should be emphasized in pyruvate effects on glucometabolic abnormalities in attenuation of diabetic status and DN.

4.2.1. Pyruvate Improved Glycolytic Pathways in Diabetes

Present data first discovered that aldose reductase (AR) was stimulated in group Con but restored by oral pyruvate treatments in groups Pyr and Pyr-ORS in diabetic db/db mice (Figure 1(b)).

It is acknowledged that the AR activity is definitely stimulated in HG and diabetes, contributing to promotion of the sorbitol pathway, additionally due to the hexokinase activity (HK) saturated in hyperglycemia, resulting in NADPH/NADP+ and NAD+/NADH ratio depletion and subsequent inhibition of the pentose phosphate pathway (PPP), which is the major source of NADPH to sustain GSH [11, 12, 28]. Oral pyruvate declined the promoted AR in diabetic db/db mice first supported the previous proposal that pyruvate competitive inhibition of AR in HG conditions [12]. Therefore, hyperglycemia/HG accounts for redox potential inhibition in diabetic tissues and organs (Figure 4). Further, as shown in Table 3, the renal PK activity, one of the key glycolytic enzymes, was also depressed in diabetic db/db mice. Anaerobic glycolytic pathway, thus, is suppressed in diabetes, as suggested as so-called pseudohypoxia, which can be significantly attenuated by antioxidant treatments [29, 30], while pyruvate is a well-recognized potent antioxidant. Both HG-induced AR stimulation and PK suppression play critical roles in DN development [3, 30]. However, present findings first comprehensively ascertained that oral pyruvate strengthened canonical glycolytic flux with a decrease of glucose toxic metabolite accumulation by (1) competitive inhibition of AR in sorbitol pathway with a rise of NAD+ and NADPH and concomitantly reversing the PPP, leading to GSH/GSSG enhancement, as shown with increases of NAD+/NADH and GSH-Px (Tables 4 and 5); (2) reversal of key glycolytic enzymes, such as HK, phosphate fructose kinase (PFK-1), and PK (PK M2 increase may also regulate TCA/mitochondrial pathways [4]), though the 2 formers were not detected; and (3) spontaneously anaerobic pyruvate reduction by the energy free LDH reductive reaction, despite attenuation of HG-raised LDH by pyruvate, coupled with NADH oxidation to NAD+, additionally raising the NAD+/NADH ratio in diabetes (Table 4), which facilitates glycolysis at the G-3PD step (glyceraldehyde-3-phosphate dehydrogenase), where NAD+ is required [30]. Consequently, the canonical anaerobic glycolysis was quite functionally revival in both oral pyruvate-treated groups of diabetic db/db mice (Figure 4).

4.2.2. Pyruvate Preserved Oxidative Metabolism in Diabetes

The pyruvate dehydrogenase (PDH) activity plays a critical role in glucose oxidative metabolism. Various pathogenic insults, including critical injuries, such as bleeding, trauma and sepsis, diabetes, aging, and even cancer, may induce the PDH inhibition, leading to specifically distinct metabolic disturbances and acid-base imbalances in various respective insults. The PDH activity is decreased in diabetic animals and humans, and clinical diabetic ketoacidosis even appears more severe PDH inhibition [31, 32]. Data here provided first evidence that oral pyruvate rejuvenated the HG-inhibited PDH activity in diabetes, as shown in Table 3, where renal PDHa/t activities were comparably enhanced in two pyruvate groups. Also, immunohistochemistry of renal PDH activities similarly showed a full restoration in two pyruvate groups in db/db mice (Figure 3(a)). Pyruvate, like dichloroacetate (DCA) as a PDH activator [33], conferred a full reactivation of the suppressed PDH in diabetic kidneys of two pyruvate groups, which was consistent with the treatment of hemorrhagic shock and brain trauma [34, 35]. Apparently, the novel finding with oral pyruvate reactivation of PDH along with PK improvement and AR inhibition in diabetic db/db mice is of robust significance in clinical treatments of diabetes and diabetic organ complications in the kidney, brain, heart, eye, and skin.

As shown in Figures 1(c)1(e), PDH and PDHA1 were inhibited, but PDK were prompted in the control group, whereas the above alterations were fully restored in two pyruvate groups. Accordingly, oral pyruvate reversal of PDH was closely associated with its inhibition of HG-enhanced PDK activity in db/db mice, as previously demonstrated that pyruvate as mimetic DCA inhibited PDK phosphorylation [36, 37]. By renovation of PDH as well as PC (pyruvate carboxylase) activity induced by pyruvate, oral pyruvate enhanced anaplerosis (replenishment of tricarboxylic acid (TCA)-cycle substrates) and the TCA cycle with sustained oxidative phosphorylation, in vivo. Accordingly, the Warburg phenomenon (aerobic glycolysis enhancement with PDH-oxidative phosphorylation inhibition in aerobic conditions) could be reversed. As a result, glucose oxidative metabolism as well as blood sugar was markedly improved, leading to delay diabetic progression in db/db mice (Figure 4). In addition, as shown in Table 1, oral pyruvate might stimulate insulin secretion from β-cells in diabetic or even nondiabetic patients [26, 27, 38]; thus, enhanced blood insulin might also activate the PDH activity, in vivo. Further, the PDH preservation might be additionally contributed with pyruvate antioxidative stress (Table 5). Furthermore, although pyruvate/lactate ratio and ATP generation in blood or kidney were not monitored in the experiment, NAD+/NADH ratio was significantly increased in diabetic kidneys following pyruvate treatments (Table 4). It was previously discovered that enteral Pyr-ORS raised blood pyruvate over 5 times with pyruvate/lactate ratio increase and corrected lethal hypoxic lactic acidosis, profoundly enhancing survival in rehydration of rats subjected to severe burn shock [23]; oral pyruvate as drinking water also markedly increased contents of ATP and ATPase in neurons of rats subjected to microgravity for 8 weeks (data submitted for publication).

All in all, present results first demonstrated that oral pyruvate fluids effectively corrected glucometabolic disturbances, particularly by reactivation of glucose oxidative phosphorylation with PDH (PDHa/t) restoration via direct PDK inhibition, in diabetic db/db mice. The pyruvate protective effects above against diabetic glucometabolic aberrances, in vivo, as AR and PDK inhibition and PDH reactivation were replicated by pyruvate in HK-2 (human renal proximal tubular epithelial) cell lines in HG conditions, in vitro (data not shown), which also showed the inhibition of ER stress and cellular apoptosis of HK-2 cells by pyruvate addition in HG [39]. A recent investigation further demonstrated that diabetes markedly inhibited mitochondrial metabolism in pancreatic β-cells, whereas early studies displayed pyruvate preservation of islet engrafts function [40, 41]. Present results that showed a consequence of rise in blood insulin levels are in consistence with these findings though islets were not investigated in the experiment.

Therefore, oral pyruvate as a novel strategy, other than current advances with sodium glucose linked transporter-2 (SGLT-2) inhibitors and glucagon-like peptide-1 (GLP-1) receptor agonists [2], treated diabetic status and DN specifically by restoration of regular glucometabolic pathways with promoting glycolysis and glucose oxidative phosphorylation to drive the HG-induced Warburg effect backwards in kidneys of the experimental diabetic db/db mice.

4.2.3. Pyruvate Delayed AGE Formation

Another novel finding that has to be noticed is that pyruvate was also shown as an AGE antagonist that parallelly inhibited renal AGEs and oxidative stress levels in two pyruvate groups in db/db mice (Tables 4 and 5), though the inflammatory inhibition was not significant with Pyr-ORS in this experimental condition (Figure 2). AGE formation as well as deposition in tissues is an important causative factor of onset and progression in diabetic organ complications, including DN via stimulating oxidative stress, angiotensinogen production, ER stress, and fibrosis in kidney [9, 42, 43]. AGE inhibitors are, at least, partially effective in DN treatments in both animal studies and clinical trials [44]. Recent findings demonstrated that pyruvate was ER stress inhibitable, in vitro, via antioxidative stress and antiapoptotic effects and resistant to the AGEs formation, in vivo, by a competitive inhibition with glucose and recover of enzyme systems that protect from glycation stress [39, 45]. Pyruvate even showed a significant role in the reversal of AGE formation and attenuated its advancement in diabetic cataract tissues, and its underlying molecular mechanism was also addressed [19, 20, 45]. The oral pyruvate effect on attenuation or prevention of AGE accumulation in diabetes may play a pivotal role in reversing the vicious cycle in DN onset and development.

4.3. Pyruvate in ORS Benefits in Clinical Diabetes

Since 2012, Pyr-ORS was first proposed to improve WHO-guided ORS (WHO-ORS I, II or III) that contains bicarbonate or citrate by equimolar pyruvate. Prior studies demonstrate that oral or enteral Pyr-ORS is more beneficial than WHO-ORS in animal shock resuscitation and kidney protection [2123]. Present data clearly illustrated that oral pyruvate in both Pyr-ORS (0.35% pyruvate) and 1% pyruvate was comparably effective to protect key enzyme activities and histopathological alterations against HG in diabetic mice (Figures 1 and 3).

In clinical settings, a patient drunk 1% pyruvate for 2 liters ingested 20 g of sodium pyruvate, but ingestion of 7-25 g pyruvate has no effectiveness or just limited function in adults due to poor absorption from intestine [46, 47]. Intestinal absorption of sodium salt requires coexisting glucose via Na+-glucose cotransporters located in gastrointestinal epithelium in mammalians [2123]. In contrast, 1% pyruvate is effective in diabetic rodents, due to feed pyruvate always in Na+-glucose fluid with drinking and eating in animals. Given the findings that two pyruvate fluids showed a basically equal effect, 0.35% pyruvate with 1.35% glucose in Pyr-ORS may be beneficial and practicable to prevent and treat diabetes in humans. Nevertheless, it is also worthy to note that oral Pyr-ORS here just delayed the DN progression, rather than fully prohibited the DN development in db/db mice. The pyruvate dosage might be not optimal; the dose-effect test and a long-term investigation are required. Further studies with a large animal group size in various models are essential to verify oral pyruvate (Pyr-ORS) effects on diabetes and DN and its effects on the protection of diabetic pancreatic β-cells. Because several clinical studies in various diseases treated with large doses (around 1.0 g/kg) of pyruvate products at the time reported that oral or systemic pyruvate administration indicated the clinical effectiveness and tolerance without adverse effects [26, 27, 38, 4850], clinical trials are safe and urgently warranted in diabetic patients with a Pyr-ORS formula modified if needed.

Finally, it is hereby notable that ethyl pyruvate (EP, a derivative of pyruvate sodium salt) has been reported for the potential intervention of diabetes and DN [51], which further strengthens pyruvate effects on diabetes. However, there is a distinct difference between EP and sodium pyruvate: EP is helpful in animals, but not in humans; the failure of a phase II clinical trial on EP may support the hypothesis, making its clinical prospective hopelessly [52, 53].

Taking together, results here suggest that oral Pyr-ORS may provide a novel strategy in pharmacologic interventions of clinical diabetes and its organ complications, even diabetic ketoacidosis and may be a novel therapeutic approach, even as a functional drink, in the prevention and treatment of diabetes and DN in a large population.

5. Conclusion

Oral Pyr-ORS has a comparable effectiveness with 1% pyruvate in the treatment of diabetes and DN development in diabetic db/db mice. Oral pyruvate may renovate glucometabolic profile, particularly inhibit HG-promoted AR activity, and reactivate HG-depressed PK and PDH, via inhibition of PDK, activities to reverse the Warburg effect in diabetic glucometabolic defects. In addition, oral pyruvate may exert antioxidative stress and inhibit AGE formation. Consequently, oral pyruvate may turn the vicious circle to a virtuous cycle of glucometabolic disorders in diabetes and DN. Further study is required particularly in the dose-response manner and long-term investigations with a large group size. A novel therapeutic strategy with Pyr-ORS may be beneficial in clinical prevention and treatment of type 2 diabetes and DN.

Abbreviations

AGEs:Advanced glycation end products
AR:Aldose reductase
Cyst C:Cystatin C
DM:Diabetes mellitus
DN:Diabetic nephropathy
ER:Endoplasmic reticulum
GSH-Px:Glutathione peroxidase
HG:High glucose
LDH:Lactate dehydrogenase
NAD(P)+/NAD(P)H:Nicotinamide adenine dinucleotide (phosphate) (oxidized/reduced form)
NGAL:Neutrophil gelatinase-associated lipocalin
ORS:Oral rehydration solution
GSH/GSSG:Glutathione (reduced/oxidized form)
PDH:Pyruvate dehydrogenase
Pyr-ORS:Pyruvate-ORS
PDHa/t:PDHactive/total
PDHA1:Active form of PDH
PDK:Pyruvate dehydrogenase kinase
PK:Pyruvate kinase
PPP:Pentose phosphate pathway
ROS:Radical oxygen species
SOD:Superoxide dismutase
TCA cycle:Tricarboxylic acid cycle.

Data Availability

Data can be provided upon requests.

Conflicts of Interest

The authors declared no conflict of interests.

Authors’ Contributions

Zhou FQ, Yang XH, and Jin HM designed experiments; Zhang XM, Deng H, Tong JD, and Wang YZ performed animal experiments, corrected data, and conducted statistical analysis; Zhou FQ, Zhang XM, and Jin HM wrote the manuscript drafts, Jin HM and Zhou FQ critically revised the manuscript. Zhang XM, Deng H, and Tong JD contributed equally to this paper.

Acknowledgments

This study was supported by Shanghai Pudong Hospital Key Discipline in Nephrology and Plasma Purification-2020 and Shanghai Municipal Health Commission (Grant no. 201840025).

References

  1. K. Ogurtsova, J. D. da Rocha Fernandes, Y. Huang et al., “IDF Diabetes Atlas: global estimates for the prevalence of diabetes for 2015 and 2040,” Diabetes Research and Clinical Practice, vol. 128, pp. 40–50, 2017. View at: Publisher Site | Google Scholar
  2. R. Z. Alicic, M. T. Rooney, and K. R. Tuttle, “Diabetic kidney disease: challenges, progress, and possibilities,” Clinical Journal of the American Society of Nephrology, vol. 12, no. 12, pp. 2032–2045, 2017. View at: Publisher Site | Google Scholar
  3. D. Gordin, H. Shah, T. Shinjo et al., “Characterization of glycolytic enzymes and pyruvate kinase M2 in type 1 and 2 diabetic nephropathy,” Diabetes Care, vol. 42, no. 7, pp. 1263–1273, 2019. View at: Publisher Site | Google Scholar
  4. G. Zhang, M. Darshi, and K. Sharma, “The Warburg effect in diabetic kidney disease,” Seminars in Nephrology, vol. 38, no. 2, pp. 111–120, 2018. View at: Publisher Site | Google Scholar
  5. W. Qi, Q. Li, D. Gordin, and G. L. King, “Preservation of renal function in chronic diabetes by enhancing glomerular glucose metabolism,” Journal of Molecular Medicine (Berlin, Germany), vol. 96, no. 5, pp. 373–381, 2018. View at: Publisher Site | Google Scholar
  6. H. Qi, G. Casalena, S. Shi et al., “Glomerular endothelial mitochondrial dysfunction is essential and characteristic of diabetic kidney disease susceptibility,” Diabetes, vol. 66, no. 3, pp. 763–778, 2017. View at: Publisher Site | Google Scholar
  7. R. Shibusawa, E. Yamada, S. Okada et al., “Dapagliflozin rescues endoplasmic reticulum stress-mediated cell death,” Scientific Reports, vol. 9, no. 1, p. 9887, 2019. View at: Publisher Site | Google Scholar
  8. T. A. Schiffer and M. Friederich-Persson, “Mitochondrial reactive oxygen species and kidney hypoxia in the development of diabetic nephropathy,” Frontiers in Physiology, vol. 8, p. 211, 2017. View at: Publisher Site | Google Scholar
  9. K. Matoba, Y. Takeda, Y. Nagai, D. Kawanami, K. Utsunomiya, and R. Nishimura, “Unraveling the role of inflammation in the pathogenesis of diabetic kidney disease,” International Journal of Molecular Sciences, vol. 20, no. 14, p. 3393, 2019. View at: Publisher Site | Google Scholar
  10. A. Kumar Pasupulati, P. S. Chitra, and G. B. Reddy, “Advanced glycation end products mediated cellular and molecular events in the pathology of diabetic nephropathy,” Biomolecular Concepts, vol. 7, no. 5-6, pp. 293–309, 2016. View at: Publisher Site | Google Scholar
  11. W. Zhao, P. S. Devamanoharan, M. Henein, A. H. Ali, and S. D. Varma, “Diabetes-induced biochemical changes in rat lens: attenuation of cataractogenesis by pyruvate,” Diabetes, Obesity & Metabolism, vol. 2, no. 3, pp. 165–174, 2000. View at: Publisher Site | Google Scholar
  12. F. Q. Zhou, “Advantages of pyruvate over lactate in peritoneal dialysis solutions,” Acta Pharmacologica Sinica, vol. 22, no. 5, pp. 385–392, 2001. View at: Google Scholar
  13. K. R. Hegde and S. D. Varma, “Morphogenetic and apoptotic changes in diabetic cataract: prevention by pyruvate,” Molecular and Cellular Biochemistry, vol. 262, no. 1/2, pp. 233–237, 2004. View at: Publisher Site | Google Scholar
  14. S. Hu, X. D. Bai, X. Q. Liu et al., “Pyruvate Ringer's solution corrects lactic acidosis and prolongs survival during hemorrhagic shock in rats,” The Journal of Emergency Medicine, vol. 45, no. 6, pp. 885–893, 2013. View at: Publisher Site | Google Scholar
  15. R. Liu, S. M. Wang, X. Q. Liu et al., “Erratum to “Pyruvate alleviates lipid peroxidation and multiple organ dysfunction in rats with hemorrhagic shock” (Am J Emerg Med 34[3]:525-530),” The American Journal of Emergency Medicine, vol. 34, no. 7, p. 1330, 2016. View at: Publisher Site | Google Scholar
  16. A. K. Salahudeen, E. C. Clark, and K. A. Nath, “Hydrogen peroxide-induced renal injury. A protective role for pyruvate in vitro and in vivo,” The Journal of Clinical Investigation, vol. 88, no. 6, pp. 1886–1893, 1991. View at: Publisher Site | Google Scholar
  17. R. A. Zager, A. C. M. Johnson, and K. Becker, “Renal cortical pyruvate depletion during AKI,” Journal of the American Society of Nephrology, vol. 25, no. 5, pp. 998–1012, 2014. View at: Publisher Site | Google Scholar
  18. S. Hu, Y. L. Dai, M. J. Gao et al., “Pyruvate as a novel carrier of hydroxyethyl starch 130/0.4 may protect kidney in rats subjected to severe burns,” Journal of Surgical Research, vol. 225, pp. 166–174, 2018. View at: Publisher Site | Google Scholar
  19. S. D. Varma, K. R. Hegde, and S. Kovtun, “Attenuation and delay of diabetic cataracts by antioxidants: effectiveness of pyruvate after onset of cataract,” Ophthalmologica, vol. 219, no. 5, pp. 309–315, 2005. View at: Publisher Site | Google Scholar
  20. K. Hegde, S. Kovtun, and S. Varma, “Prevention of cataract in diabetic mice by topical pyruvate,” Clinical Ophthalmology, vol. 5, pp. 1141–1145, 2011. View at: Publisher Site | Google Scholar
  21. W. Yu, S. Hu, Z. Y. Xie et al., “Pyruvate oral rehydration solution improved visceral function and survival in shock rats,” The Journal of Surgical Research, vol. 193, no. 1, pp. 344–354, 2015. View at: Publisher Site | Google Scholar
  22. R. Liu, X. H. Hu, S. M. Wang et al., “Pyruvate in oral rehydration salt improves hemodynamics, vasopermeability and survival after burns in dogs,” Burns, vol. 42, no. 4, pp. 797–806, 2016. View at: Publisher Site | Google Scholar
  23. R. Liu, S. M. Wang, Z. Y. Li, W. Yu, H. P. Zhang, and F. Q. Zhou, “Pyruvate in reduced osmolarity oral rehydration salt corrected lactic acidosis in sever scald rats,” The Journal of Surgical Research, vol. 226, pp. 173–180, 2018. View at: Publisher Site | Google Scholar
  24. I. Chang, N. Cho, J. Y. Koh, and M. S. Lee, “Pyruvate inhibits zinc-mediated pancreatic islet cell death and diabetes,” Diabetologia, vol. 46, no. 9, pp. 1220–1227, 2003. View at: Publisher Site | Google Scholar
  25. C. T. Sheline, C. Shi, T. Takata et al., “Dietary zinc reduction, pyruvate supplementation, or zinc transporter 5 knockout attenuates β-cell death in nonobese diabetic mice, islets, and insulinoma cells,” The Journal of Nutrition, vol. 142, no. 12, pp. 2119–2127, 2012. View at: Publisher Site | Google Scholar
  26. I. Petkova, V. Hristov, K. Petrov, and W. Thorn, “Oral application of sodium pyruvate in healthy persons and patients with diabetes mellitus type 1,” Comptes rendus de I’Academie bulgare des Sci Medecine Clinique, vol. 60, pp. 579–584, 2007. View at: Google Scholar
  27. T. Inoue, N. Murakami, T. Ayabe et al., “Pyruvate improved insulin secretion status in a mitochondrial diabetes mellitus patient,” The Journal of Clinical Endocrinology and Metabolism, vol. 101, no. 5, pp. 1924–1926, 2016. View at: Publisher Site | Google Scholar
  28. L. J. Yan, “Redox imbalance stress in diabetes mellitus: role of the polyol pathway,” Animal Models and Experimental Medicine, vol. 1, no. 1, pp. 7–13, 2018. View at: Publisher Site | Google Scholar
  29. J. Song, X. Yang, and L. J. Yan, “Role of pseudohypoxia in the pathogenesis of type 2 diabetes,” Hypoxia, vol. 7, pp. 33–40, 2019. View at: Publisher Site | Google Scholar
  30. C. Laustsen, P. M. Nielsen, T. S. Nørlinger et al., “Antioxidant treatment attenuates lactate production in diabetic nephropathy,” American Journal of Physiology-Renal Physiology, vol. 312, no. 1, pp. F192–F199, 2017. View at: Publisher Site | Google Scholar
  31. M. Mostert, I. Rabbone, M. Piccinini et al., “Derangements of pyruvate dehydrogenase in circulating lymphocytes of NIDDM patients and their healthy offspring,” Journal of Endocrinological Investigation, vol. 22, no. 7, pp. 519–526, 1999. View at: Publisher Site | Google Scholar
  32. L. W. Andersen, K. M. Berg, S. Montissol et al., “Pyruvate dehydrogenase activity is decreased in emergency department patients with diabetic ketoacidosis,” Academic Emergency Medicine, vol. 23, no. 6, pp. 685–689, 2016. View at: Publisher Site | Google Scholar
  33. R. Jaimes 3rd, S. Kuzmiak-Glancy, D. M. Brooks, L. M. Swift, N. G. Posnack, and M. W. Kay, “Functional response of the isolated, perfused normoxic heart to pyruvate dehydrogenase activation by dichloroacetate and pyruvate,” Pflügers Archiv - European Journal of Physiology, vol. 468, no. 1, pp. 131–142, 2016. View at: Publisher Site | Google Scholar
  34. P. Sharma, K. T. Walsh, K. A. Kerr-Knott, J. E. Karaian, and P. D. Mongan, “Pyruvate modulates hepatic mitochondrial functions and reduces apoptosis indicators during hemorrhagic shock in rats,” Anesthesiology, vol. 103, no. 1, pp. 65–73, 2005. View at: Publisher Site | Google Scholar
  35. P. Sharma, B. Benford, Z. Z. Li, and G. S. F. Ling, “Role of pyruvate dehydrogenase complex in traumatic brain injury and measurement of pyruvate dehydrogenase enzyme by dipstick test,” Journal of Emergencies, Trauma, and Shock, vol. 2, no. 2, pp. 67–72, 2009. View at: Publisher Site | Google Scholar
  36. D. A. Priestman, K. A. Orfali, and M. C. Sugden, “Pyruvate inhibition of pyruvate dehydrogenase kinase. Effects of progressive starvation and hyperthyroidism in vivo, and of dibutyryl cyclic AMP and fatty acids in cultured cardiac myocytes,” FEBS Letters, vol. 393, no. 2-3, pp. 174–178, 1996. View at: Publisher Site | Google Scholar
  37. Y. Saiki, G. D. Lopaschuk, K. Dodge, K. Yamaya, C. Morgan, and I. M. Rebeyka, “Pyruvate augments mechanical function via activation of the pyruvate dehydrogenase complex in reperfused ischemic immature rabbit hearts,” The Journal of Surgical Research, vol. 79, no. 2, pp. 164–169, 1998. View at: Publisher Site | Google Scholar
  38. H. Nagasaka, H. Komatsu, A. Inui et al., “Circulating tricarboxylic acid cycle metabolite levels in citrin-deficient children with metabolic adaptation, with and without sodium pyruvate treatment,” Molecular Genetics and Metabolism, vol. 120, no. 3, pp. 207–212, 2017. View at: Publisher Site | Google Scholar
  39. X. M. Zhang, Y. Z. Wang, J. D. Tong et al., “Pyruvate alleviates high glucose-induced endoplasmic reticulum stress and apoptosis in HK-2 cells,” FEBS Open Bio, vol. 10, no. 5, pp. 827–834, 2020. View at: Publisher Site | Google Scholar
  40. E. Haythorne, M. Rohm, M. van de Bunt et al., “Diabetes causes marked inhibition of mitochondrial metabolism in pancreatic β-cells,” Nature Communications, vol. 10, no. 1, p. 2474, 2019. View at: Publisher Site | Google Scholar
  41. M. L. Brown, M. Braun, L. Cicalese, and C. Rastellini, “Effect of perioperative antioxidant therapy on suboptimal islet transplantation in rats,” Transplantation Proceedings, vol. 37, no. 1, pp. 217–219, 2005. View at: Publisher Site | Google Scholar
  42. J. M. Garagliano, A. Katsurada, K. Miyata et al., “Advanced glycation end products stimulate angiotensinogen production in renal proximal tubular cells,” The American Journal of the Medical Sciences, vol. 357, no. 1, pp. 57–66, 2019. View at: Publisher Site | Google Scholar
  43. K. H. Huang, S. S. Guan, W. H. Lin et al., “Role of Calbindin-D28k in diabetes-associated advanced glycation end-products-induced renal proximal tubule cell injury,” Cells, vol. 8, no. 7, p. 660, 2019. View at: Publisher Site | Google Scholar
  44. P. Jud and H. Sourij, “Therapeutic options to reduce advanced glycation end products in patients with diabetes mellitus: a review,” Diabetes Research and Clinical Practice, vol. 148, pp. 54–63, 2019. View at: Publisher Site | Google Scholar
  45. G. F. Scott, A. Q. Nguyen, B. H. Cherry et al., “Featured article: pyruvate preserves antiglycation defenses in porcine brain after cardiac arrest,” Experimental Biology and Medicine, vol. 242, no. 10, pp. 1095–1103, 2017. View at: Publisher Site | Google Scholar
  46. M. A. Morrison, L. L. Spriet, and D. J. Dyck, “Pyruvate ingestion for 7 days does not improve aerobic performance in well-trained individuals,” Journal of Applied Physiology, vol. 89, no. 2, pp. 549–556, 2000. View at: Publisher Site | Google Scholar
  47. R. A. Olek, M. Luszczyk, S. Kujach et al., “Single pyruvate intake induces blood alkalization and modification of resting metabolism in humans,” Nutrition, vol. 31, no. 3, pp. 466–474, 2015. View at: Publisher Site | Google Scholar
  48. M. L. Krinsky and M. D. Topazian, “A novel approach to common bile duct stone extraction,” Gastrointestinal Endoscopy, vol. 46, no. 4, pp. 382-383, 1997. View at: Publisher Site | Google Scholar
  49. W. Schillinger, M. Hünlich, S. Sossalla, H. P. Hermann, and G. Hasenfuss, “Intracoronary pyruvate in cardiogenic shock as an adjunctive therapy to catecholamines and intra-aortic balloon pump shows beneficial effects on hemodynamics,” Clinical Research in Cardiology, vol. 100, no. 5, pp. 433–438, 2011. View at: Publisher Site | Google Scholar
  50. Y. Koga, N. Povalko, E. Inoue, K. Nashiki, and M. Tanaka, “Biomarkers and clinical rating scales for sodium pyruvate therapy in patients with mitochondrial disease,” Mitochondrion, vol. 48, pp. 11–15, 2019. View at: Publisher Site | Google Scholar
  51. J. H. Jun, J. W. Song, E. J. Shin, Y. L. Kwak, N. Choi, and J. K. Shim, “Ethyl pyruvate is renoprotective against ischemia-reperfusion injury under hyperglycemia,” The Journal of Thoracic and Cardiovascular Surgery, vol. 155, no. 4, pp. 1650–1658, 2018. View at: Publisher Site | Google Scholar
  52. F. Q. Zhou, “Pyruvate research and clinical application outlooks a revolutionary medical advance,” International Journal of Nutrition, vol. 5, no. 1, pp. 1–9, 2020. View at: Publisher Site | Google Scholar
  53. E. Bennett-Guerrero, M. Swaminathan, A. M. Grigore et al., “A phase II multicenter double-blind placebo-controlled study of ethyl pyruvate in high-risk patients undergoing cardiac surgery with cardiopulmonary bypass,” Journal of Cardiothoracic and Vascular Anesthesia, vol. 23, no. 3, pp. 324–329, 2009. View at: Publisher Site | Google Scholar

Copyright © 2020 Xiao Meng Zhang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder
Views312
Downloads303
Citations

Related articles

Article of the Year Award: Outstanding research contributions of 2020, as selected by our Chief Editors. Read the winning articles.