PPAR Research

PPAR Research / 2020 / Article
Special Issue

The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Disease and Targeted Treatments

View this Special Issue

Research Article | Open Access

Volume 2020 |Article ID 8889612 | https://doi.org/10.1155/2020/8889612

Hua Guo, Qinglan Zhang, Haipo Yuan, Lin Zhou, Fang-fang Li, Sheng-Ming Wang, Gang Shi, Maojuan Wang, "Nitric Oxide Mediates Inflammation in Type II Diabetes Mellitus through the PPARγ/eNOS Signaling Pathway", PPAR Research, vol. 2020, Article ID 8889612, 7 pages, 2020. https://doi.org/10.1155/2020/8889612

Nitric Oxide Mediates Inflammation in Type II Diabetes Mellitus through the PPARγ/eNOS Signaling Pathway

Academic Editor: Xiao-Jie Lu
Received15 Sep 2020
Revised12 Oct 2020
Accepted12 Nov 2020
Published27 Nov 2020

Abstract

Inflammation accounts for the process of type II diabetes mellitus (T2DM), the specific mechanism of which is still to be elucidated yet. Nitric oxide (NO), a critical inflammation regulator, the role of which is the inflammation of T2DM, is rarely reported. Therefore, our study is aimed at exploring the effect of NO on the inflammation in T2DM and the corresponding mechanism. We analyzed the NO levels in plasma samples from T2DM patients and paired healthy adults by Nitric Oxide Analyzer then measured the expression of inflammatory cytokines (C-reactive protein, heptoglobin, IL-1β, TNF-α, IL-6) in insulin-induced HepG2 cells treated with NO donor or NO scavenger, and the PPARγ, eNOS, C-reactive protein, heptoglobin, IL-1β, TNF-α, and IL-6 levels were detected by RT-PCR and western blot in insulin-induced HepG2 cells transfected with si-PPARγ. The results showed that excess NO increased the inflammation marker levels in T2DM, which is activated by the PPARγ/eNOS pathway. These findings will strengthen the understanding of NO in T2DM and provide a new target for the treatment of T2DM.

1. Introduction

Type II diabetes mellitus (T2DM) is a common chronic metabolic and endocrine disease characterized by insulin resistance and β-cell dysfunction. The high prevalence of T2DM is a serious public health event over the world [1]. According to the latest data given by the Chinese Diabetes Society (CDS), the incidence of T2DM in adults over the age of 18 in China is increasing annually and up to 10.4% by 2019 [2]. Studies have shown that the onset of T2DM is associated with a complex interaction between environmental and genetic factors [3, 4], and the specific pathogenesis of the disease has yet to be elucidated. It has been reported that chronic inflammatory responses may be involved in the process of insulin resistance and β-cell dysfunction, which adds the risk of developing T2DM [5, 6]. C-reactive protein can lead to insulin resistance and is an important indicator of the level of inflammation in T2DM [5, 7]. Haptoglobin is an important indicator of liver inflammation, and it is shown that the haptoglobin 2-2 genotype might increase the risk of cardiovascular disease in diabetic patients [8, 9]. Inflammatory factors such as TNF-α, IL-1β, and IL-6 have been clarified to cause insulin resistance by inhibiting insulin signaling [10, 11]. Therefore, actively exploring the mechanisms of inflammation in T2DM can provide new ideas for the treatment of the disease.

PPARγ belongs to a family of peroxisome proliferator-activated nuclear receptors that regulate the expression of multiple genes involved in the regulation of lipid/glucose/amino acid metabolism, cell proliferation/differentiation, and inflammation, suggesting that it may play important roles in many diseases [12]. Thiazolidinedione, a target drug of PPARγ, has potent insulin-sensitizing effects and is used to treat T2DM, but the drug will produce side effects such as weight gain, liver damage, and cardiovascular risk and is gradually declining in clinical use [13, 14]. Thus, it is extremely important to clarify the mechanism of PPARγ in T2DM. In recent years, studies have told that PPARγ regulates the expression of inflammatory pathways. For example, GMG-43AC antagonist can be applied to treat acne because it activates PPARγ to inhibit inflammation [12]. PPARγ-mediated upregulation of CD36 is involved in the regulation of microglial activation and phenotype and promotes phagocyte-cell proliferation of apoptotic cells, thereby promoting the recovery of postischemic inflammation [15]. Moreover, PPARγ activation is essential in the suppression of intestinal inflammatory response [16]. In T2DM, the detailed mechanism by which PPARγ regulates inflammation remains to be refined.

Nitric oxide (NO), a free radical molecule with pathophysiological functions, is extensively studied in inflammation. NO has anti-inflammatory and proinflammatory effects, which are correlated with its concentration [17]. Excess NO will damage cells and organs and interacts with intermediate components of reactive oxygen species in cells to induce inflammation [18]. Studies have indicated that the NO/inflammatory signaling pathway is associated with the development of depression [19], colon cancer [20], lung squamous cell carcinoma [18], and diabetes [21]. Endothelial nitric oxide synthase (eNOS) is a kind of nitric oxide synthase that induces NO production, occupying the dominant role in regulating NO activity [22]. Previous studies have shown that the PPARγ/eNOS pathway regulates hypertension [23], ischemia/reperfusion-induced acute kidney injury [24], steatohepatitis [25], ischemia/reperfusion-induced liver injury [26], and so on. However, it is not clear whether the PPARγ/eNOS pathway mediates the inflammatory process in T2DM.

Therefore, we put forward the hypothesis that NO may regulate inflammation in T2DM through the PPARγ/eNOS pathway and validated in the present study. Our findings may provide a new treatment target for T2DM.

2. Materials and Methods

2.1. Blood Collection from T2DM Patients

The study was approved by the ethics committee of Huai’an Second People’s Hospital and Hospital of Chengdu University of Traditional Chinese Medicine. Fifty-five T2DM patients and fifty healthy adults in this study signed informed consent forms and began to sample blood at 8:30 am in the morning under a fasting state (no food and water absorption for at least 8 h before sampling). The whole blood samples were collected and placed in a heparin anticoagulation tube (BD, USA), then centrifuged at 3500 g at 4°C for 10 min. The achieved uppermost layer is the plasma layer, which should be stored at -80°C for subsequent testing.

2.2. Cell Culture

HepG2 cells were purchased from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China); they were cultured in 96-well plates in RPMI1640 medium (Gibco, NY, USA) with 10% fetal bovine serum (Gibco, USA) and 1% penicillin-streptomycin (Gibco, NY, USA) and allowed to grow to logarithmic growth phase for subsequent studies after a successful recovery. To construct a cell model of T2DM, insulin (Gibco, NY, USA) was first diluted in RPMI1640 complete medium to a final concentration of 10-6 mol/L. 200 μL of insulin preparation solution was added to each well in the model group, and an equal amount of RPMI1640 complete medium was added to each well in the control group; all cells were cultured for 48 h [27]. In the process of cultivation, cells were incubated in an incubator (37°C, 5% CO2).

2.3. RNA Interference

HepG2 cells were transfected with 100 pmol PPARγsiRNA (sense, 5-UAAAUGUCAGUACUGUCGGUUU-3, antisense, 5-CCGACAGUACUGACAUUUAUU-3) by using the Amaxa Lonza Cell Line Nucleofector® Kit (Lonza, Germany) according to the manufacturer’s instructions, and an equal amount of nonspecific siRNA (sense, 5-UUCUCCGAACGUGUCACGU-3; antisense, 5-(ACGUGACACGUUCGGAGAA-3) was transfected with HepG2 cells as a negative control. After incubation for 24 h, they were used for western blot analysis.

2.4. The Measurement of Nitric Oxide

Due to the fact that NO has a short half-life and is not easy to directly detect, the concentration of its stable metabolites nitrite and nitrate can represent the levels of NO [28]. In the present study, nitrite and nitrate in plasma and cells were measured using the Nitric Oxide Analyzer 280i (GE, USA), and there is no need for pretreatment samples before testing. Each sample was tested 3 times.

2.5. ELISA Assay

The levels of IL-1β, TNF-α, and IL-6 in HepG2 cells were detected using an ELISA kit (SPI-BIO, Bertin Pharma, France), and each experiment was performed 3 times according to the manufacturer’s instructions.

2.6. Real-Time Quantitative PCR

Total RNA was isolated from cells using TRIzol reagent (Life Technologies, NY, USA) then reverse transcribed into single-stranded cDNA using a Prime ScriptTMRT kit (Takara, Dalian, China). Real-time PCR equipment (7500 Real-Time PCR System, USA) was to detect the expression of C-reactive protein, haptoglobin, eNOS, and PPARγ. The expression levels were analyzed by the -ΔΔ2Ct method, and GADPH (5-AGGTCGGAGTCAACGGATTT-3 (forward) and 5-TAGTTGAGGTCAATGAAGGG-3 (reverse)) expression levels were used as the reference standard.

2.7. Western Blot

After HepG2 cells were treated with RIPA lysis buffer (Sigma, USA), 30 μg of total protein was isolated on 12% SDS-PAGE and transferred to PVDF membranes. Membrane blotting was first blocked with 5% bovine serum albumin (Sigma, USA) for 1 h then incubated with primary antibody (anti-C-reactive protein, antihaptoglobin, antieNOS, anti-PPARγ) overnight at 4°C, followed by incubation with horseradish peroxidase for 2 h at room temperature. The relative protein expression levels were normalized to GAPDH.

2.8. Data Analysis

All statistics were analyzed using GraphPad Prism 7.0 software (USA), and all experimental data were expressed as . Whether the expression of nitrite, nitrate, and NO differed between the different groups was obtained by -test analysis. And indicates statistical significance.

3. Results

3.1. High NO Production in Plasma in T2DM Patients

To evaluate the effect of NO in the T2DM, we firstly examined the levels of nitrite and nitrate in plasma between 55 T2DM patients and paired 50 healthy adults (control group). The clinical data of volunteers in the study is shown in Table 1.


T2DM ()Control ()
 Age (yrs)34-5032-51
 Gender (M/F)34/2130/20
 Plasma nitrite (μM)<0.0001
 Plasma nitrate (μM)<0.0001

MFMF
 Plasma nitrite (μM)0.27850.5689
 Plasma nitrate (μM)0.54310.5408

The concentration of plasma nitrite in the T2DM group was significantly higher than the concentration of plasma nitrate in the control group (), and the plasma nitrate levels between the T2DM group and control group were evidently different (), which was found in Figures 1(a) and 1(b). Else, as shown in Figures 1(c) and 1(d), we also found that there were no significant gender differences in plasma nitrite or nitrate contents in the T2DM group and control group. This status revealed the abnormal NO expression in T2DM patients.

3.2. NO Promoted Inflammation in Insulin-Induced HepG2 Cells

NO regulates inflammation, and inflammation promotes the development of T2DM. To investigate whether NO is involved in inflammation in T2DM, we first stimulated HepG2 cells with insulin in vitro to obtain a cell model of T2DM in this study. The cells were then treated with the NO donor DEA (Sigma, USA) and NO scavenger 2-(4-carboxyphenyl)-4, 4, 5, 5-tetramethylimidazoline-1-oxyl-3-oxide (Sigma, USA), respectively. The concentration of IL-1β, TNF-α, and IL-6 is expressed in Table 2. Compared with insulin-induced HepG2 cells, the levels of the inflammatory factors IL-1β, TNF-α, IL-6, C-reactive protein, and heptoglobin in the cells supplied with NO donor were significantly increased, while the levels of these inflammatory factors were significantly decreased in cells treated with NO scavenger, as shown in Figure 2. The above results indicate that the level of NO correlates with the degree of T2DM inflammation.


Cytokines (ng/mL)Insulin-stimulated HepG2 cellsInsulin-stimulated HepG2 cells+NO donorInsulin-stimulated HepG2 cells+NO scavenger

TNF-α
IL-1β
IL-6

3.3. PPARγ/eNOS/NO Signaling Is Associated with Inflammation in T2DM

To investigate the mechanism of the development of inflammation in T2DM, we detected the expression of eNOS and NO in vitro. As shown in Figures 3(a) and 3(b), the expression of eNOS and NO was significantly reduced in insulin-treated HepG2 cells after the addition of the NOS inhibitor L-NAME (Cayman, USA), which suggested that the abnormal expression of NO in T2DM might be related to the abnormal expression of eNOS. Considering that PPARγ can modulate the level of diabetic inflammation, the PPARγ/eNOS pathway plays an important role in several diseases. In the present study, insulin-induced HepG2 cells transfected with PPARγ siRNA were found to significantly decrease the expression of PPARγ, eNOS, and NO in Figures 3(b) and 3(c). In addition, Figures 3(c) and 3(d) showed that the inhibition of the PPARγ expression in HepG2 cells prompted a significant decrease in the expression levels of IL-1β, TNF-α, IL-6, C-reactive protein, and heptoglobin. These results suggest that inflammation in T2DM may be associated with the PPARγ/eNOS/NO pathway.

4. Discussion

The inflammatory response can drive the pathological process of T2DM by leading to deleterious effects on tissue function and insulin resistance [10, 29], so exploring the mechanisms of inflammation in T2DM may be extremely important for the treatment of T2DM that currently lacks an effective cure. NO plays significant roles in the inflammatory process and is a potential target for the treatment of inflammatory diseases [30]. In this study, plasma samples collected from 55 T2DM patients were analyzed by Nitric Oxide Analyzer for the first time, and the sample numbers were higher than the previous publications; the results showed higher levels of nitrite and nitrate in the plasma of the T2DM patients. Similarly, it also showed that abnormal levels of nitrogen oxides in plasma, serum and urine samples of T2DM patients before [31, 32]. It suggests that NO may play an important effect in the pathogenesis of T2DM.

In vitro experiment revealed that the concentration of inflammatory factors (C-reactive protein, heptoglobin, IL-1β, TNF-α, IL-6) was significantly increased in insulin-induced HepG2 cells after NO donor treatment, while the levels of inflammatory factors were decreased in insulin-induced HepG2 cells stimulated with NO scavenger. The results support that NO may take part in the inflammatory process in T2DM patients. To investigate the mechanism of NO on inflammation in T2DM, we investigated and conducted further studies. Previous studies have shown that PPARγ hyperglycosylation modification induces endothelial insulin resistance and dysfunction associated with diabetic vascular complications by regulating the eNOS-NO pathway [33]. PPARγ provides assistance to the expression of eNOS [24], which induces NO production. However, whether NO can regulate T2DM inflammation through the PPARγ-eNOS signaling pathway is currently unclear.

To test the hypothesis, this study detected the expression of eNOS and PPARγ in vitro and found that the expression of eNOS and NO decreased after the treatment of insulin-induced HepG2 cells with NOS inhibitor. Inhibiting the expression of PPARγ in insulin-induced HepG2 cells significantly decreased the levels of PPARγ, eNOS, and NO, and the levels of C-reactive protein, heptoglobin, IL-1β, TNF-α, and IL-6 were significantly reduced. Therefore, the expression of T2DM inflammation may be regulated through the PPARγ/eNOS pathway-mediated expression of NO.

In summary, this study explored the link between NO and inflammation through insulin-induced HepG2 cells, which provides a potential therapeutic target for the possible treatment of T2DM.

Data Availability

All data are available upon request.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Hua Guo, Qinglan Zhang, and Haipo Yuan are co-first authors.

References

  1. D. Rahelić, “SEDMO IZDANJE IDF DIJABETES ATLASA--POZIV NA TRENUTNU AKCIJU [7TH edition of IDF diabetes atlas--CALL for immediate action],” Lijec̆nic̆ki Vjesnik, vol. 138, no. 1-2, pp. 57-58, 2016. View at: Google Scholar
  2. W. Jia, J. Weng, D. Zhu et al., “Standards of medical care for type 2 diabetes in China 2019,” Diabetes/Metabolism Research and Reviews, vol. 35, no. 6, article e3158, 2019. View at: Publisher Site | Google Scholar
  3. R. E. Soccio, E. R. Chen, S. R. Rajapurkar et al., “Genetic variation determines PPARγ function and anti-diabetic drug response in vivo,” Cell, vol. 162, no. 1, pp. 33–44, 2015. View at: Publisher Site | Google Scholar
  4. A. Desiderio, R. Spinelli, M. Ciccarelli et al., “Epigenetics: spotlight on type 2 diabetes and obesity,” Journal of Endocrinological Investigation, vol. 39, no. 10, pp. 1095–1103, 2016. View at: Publisher Site | Google Scholar
  5. P. H. Black, “The inflammatory response is an integral part of the stress response: implications for atherosclerosis, insulin resistance, type II diabetes and metabolic syndrome X,” Brain, Behavior, and Immunity, vol. 17, no. 5, pp. 350–364, 2003. View at: Publisher Site | Google Scholar
  6. H. Blaser, C. Dostert, T. W. Mak, and D. Brenner, “TNF and ROS crosstalk in inflammation,” Trends in Cell Biology, vol. 26, no. 4, pp. 249–261, 2016. View at: Publisher Site | Google Scholar
  7. T. Reinehr, B. Karges, T. Meissner et al., “Inflammatory markers in obese adolescents with type 2 diabetes and their relationship to hepatokines and adipokines,” The Journal of Pediatrics, vol. 173, pp. 131–135, 2016. View at: Publisher Site | Google Scholar
  8. I. Hochberg, E. M. Berinstein, U. Milman, C. Shapira, and A. P. Levy, “Interaction between the haptoglobin genotype and vitamin E on cardiovascular disease in diabetes,” Current Diabetes Reports, vol. 17, no. 6, p. 42, 2017. View at: Publisher Site | Google Scholar
  9. R. Dalan and G. Liuh Ling, “The protean role of haptoglobin and haptoglobin genotypes on vascular complications in diabetes mellitus,” European Journal of Preventive Cardiology, vol. 25, no. 14, pp. 1502–1519, 2018. View at: Publisher Site | Google Scholar
  10. M. Y. Donath and S. E. Shoelson, “Type 2 diabetes as an inflammatory disease,” Nature Reviews Immunology, vol. 11, no. 2, pp. 98–107, 2011. View at: Publisher Site | Google Scholar
  11. T. Reinehr and C. L. Roth, “Inflammation markers in type 2 diabetes and the metabolic syndrome in the pediatric population,” Current Diabetes Reports, vol. 18, no. 12, p. 131, 2018. View at: Publisher Site | Google Scholar
  12. A. Mastrofrancesco, M. Ottaviani, G. Cardinali et al., “Pharmacological PPARγ modulation regulates sebogenesis and inflammation in SZ95 human sebocytes,” Biochemical Pharmacology, vol. 138, pp. 96–106, 2017. View at: Publisher Site | Google Scholar
  13. R. E. Soccio, E. R. Chen, and M. A. Lazar, “Thiazolidinediones and the promise of insulin sensitization in type 2 diabetes,” Cell Metabolism, vol. 20, no. 4, pp. 573–591, 2014. View at: Publisher Site | Google Scholar
  14. B. Gross, M. Pawlak, P. Lefebvre, and B. Staels, “PPARs in obesity-induced T2DM, dyslipidaemia and NAFLD,” Nature Reviews Endocrinology, vol. 13, no. 1, pp. 36–49, 2017. View at: Publisher Site | Google Scholar
  15. I. Ballesteros, M. I. Cuartero, J. M. Pradillo et al., “Rosiglitazone-induced CD36 up-regulation resolves inflammation by PPARγ and 5-LO-dependent pathways,” Journal of Leukocyte Biology, vol. 95, no. 4, pp. 587–598, 2014. View at: Publisher Site | Google Scholar
  16. D. Serra, L. M. Almeida, and T. C. P. Dinis, “Anti-inflammatory protection afforded by cyanidin-3-glucoside and resveratrol in human intestinal cells via Nrf2 and PPAR-γ: comparison with 5-aminosalicylic acid,” Chemico-Biological Interactions, vol. 260, pp. 102–109, 2016. View at: Publisher Site | Google Scholar
  17. N. B. Janakiram and C. V. Rao, “iNOS-selective inhibitors for cancer prevention: promise and progress,” Future Medicinal Chemistry, vol. 4, no. 17, pp. 2193–2204, 2012. View at: Publisher Site | Google Scholar
  18. Z. Gray, G. Shi, X. Wang, and Y. Hu, “Macrophage inducible nitric oxide synthase promotes the initiation of lung squamous cell carcinoma by maintaining circulated inflammation,” Cell Death & Disease, vol. 9, no. 6, p. 642, 2018. View at: Publisher Site | Google Scholar
  19. M. Ghasemi, “Nitric oxide: antidepressant mechanisms and inflammation,” Advances in Pharmacology, vol. 86, pp. 121–152, 2019. View at: Publisher Site | Google Scholar
  20. N. Stettner, C. Rosen, B. Bernshtein et al., “Induction of nitric-oxide metabolism in enterocytes alleviates colitis and inflammation-associated colon cancer,” Cell Reports, vol. 23, no. 7, pp. 1962–1976, 2018. View at: Publisher Site | Google Scholar
  21. D. Kumar, K. Shankar, S. Patel et al., “Chronic hyperinsulinemia promotes meta-inflammation and extracellular matrix deposition in adipose tissue: implications of nitric oxide,” Molecular and Cellular Endocrinology, vol. 477, pp. 15–28, 2018. View at: Publisher Site | Google Scholar
  22. L. Xu, S. Wang, B. Li, A. Sun, Y. Zou, and J. Ge, “A protective role of ciglitazone in ox-LDL-induced rat microvascular endothelial cells via modulating PPARγ-dependent AMPK/eNOS pathway,” Journal of Cellular and Molecular Medicine, vol. 19, no. 1, pp. 92–102, 2015. View at: Publisher Site | Google Scholar
  23. L. Xiao, J. H. Dong, X. Teng et al., “Hydrogen sulfide improves endothelial dysfunction in hypertension by activating peroxisome proliferator-activated receptor delta/endothelial nitric oxide synthase signaling,” Journal of Hypertension, vol. 36, no. 3, pp. 651–665, 2018. View at: Publisher Site | Google Scholar
  24. A. P. Singh, N. Singh, D. Pathak, and P. M. S. Bedi, “Estradiol attenuates ischemia reperfusion-induced acute kidney injury through PPAR-γ stimulated eNOS activation in rats,” Molecular and Cellular Biochemistry, vol. 453, no. 1-2, pp. 1–9, 2019. View at: Publisher Site | Google Scholar
  25. Y. Yamada, M. Eto, Y. Ito et al., “Suppressive role of PPARγ-regulated endothelial nitric oxide synthase in adipocyte lipolysis,” PLoS One, vol. 10, no. 8, article e0136597, 2015. View at: Publisher Site | Google Scholar
  26. K. K. Kuo, B. N. Wu, E. Y. Chiu et al., “NO donor KMUP-1 improves hepatic ischemia-reperfusion and hypoxic cell injury by inhibiting oxidative stress and pro-inflammatory signaling,” International Journal of Immunopathology and Pharmacology, vol. 26, no. 1, pp. 93–106, 2013. View at: Publisher Site | Google Scholar
  27. Z. J. Mao, M. Lin, X. Zhang, and L. P. Qin, “Combined use of astragalus polysaccharide and berberine attenuates insulin resistance in IR-HepG2 cells via regulation of the gluconeogenesis signaling pathway,” Frontiers in Pharmacology, vol. 10, p. 1508, 2019. View at: Publisher Site | Google Scholar
  28. E. Goshi, G. Zhou, and Q. He, “Nitric oxide detection methods in vitro and in vivo,” Medical Gas Research, vol. 9, no. 4, pp. 192–207, 2019. View at: Publisher Site | Google Scholar
  29. K. Eguchi and R. Nagai, “Islet inflammation in type 2 diabetes and physiology,” The Journal of Clinical Investigation, vol. 127, no. 1, pp. 14–23, 2017. View at: Publisher Site | Google Scholar
  30. Y. Kobayashi, “The regulatory role of nitric oxide in proinflammatory cytokine expression during the induction and resolution of inflammation,” Journal of Leukocyte Biology, vol. 88, no. 6, pp. 1157–1162, 2010. View at: Publisher Site | Google Scholar
  31. N. Jelić-Knezović, S. Galijašević, M. Lovrić, M. Vasilj, S. Selak, and I. Mikulić, “Levels of nitric oxide metabolites and myeloperoxidase in subjects with type 2 diabetes mellitus on metformin therapy,” Experimental and Clinical Endocrinology & Diabetes, vol. 127, no. 1, pp. 56–61, 2019. View at: Publisher Site | Google Scholar
  32. S. Apakkan Aksun, B. Özmen, D. Özmen et al., “Serum and urinary nitric oxide in type 2 diabetes with or without microalbuminuria: relation to glomerular hyperfiltration,” Journal of Diabetes and its Complications, vol. 17, no. 6, pp. 343–348, 2003. View at: Publisher Site | Google Scholar
  33. W. Yuan, C. Ma, Y. Zhou, M. Wang, G. Zeng, and Q. Huang, “Negative regulation of eNOS-NO signaling by over-SUMOylation of PPARγ contributes to insulin resistance and dysfunction of vascular endothelium in rats,” Vascular Pharmacology, vol. 122-123, article 106597, 2019. View at: Publisher Site | Google Scholar

Copyright © 2020 Hua Guo 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
Views234
Downloads189
Citations

Related articles