Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 8031039 | 11 pages | https://doi.org/10.1155/2019/8031039

Anemoside B4 Protects Rat Kidney from Adenine-Induced Injury by Attenuating Inflammation and Fibrosis and Enhancing Podocin and Nephrin Expression

Academic Editor: Mayank Thakur
Received11 Nov 2018
Revised24 Dec 2018
Accepted27 Mar 2019
Published02 May 2019

Abstract

Anemoside B4 (B4) isolated from Radix Pulsatilla has anti-inflammatory activities in the colon and antitumor effects. However, its role in the prevention and treatment of kidney injury has not been reported. Here, we reported the effects of B4 on chronic kidney injury (CKI) and studied its related mechanism based on an adenine-induced kidney injury model in rats. The results showed that serum BUN (blood urea nitrogen), Crea (creatinine), and urinary proteins increased significantly after oral administration of adenine. Meanwhile, the adenine contents in both renal tissue and urine increased markedly compared with those of normal rats. Moreover, IL-1β, IL-6, TNFα, and NFκB expression was upregulated in the kidney. Simultaneously, the expression of NLRP3 (the nucleotide-binding and oligomerization domain–like receptor, leucine-rich repeat and pyrin domain–containing 3) in the inflammasome, which consists of Caspase 1, ASC (apoptosis-associated speck-like protein containing a caspase recruitment domain), and IL-18, was significantly upregulated. B4 could significantly decrease BUN and Crea; reduce urinary proteins in rats; suppress the expression of IL-6, IL-1β, NFκB, NLRP3, Caspase 1, ASC, and IL-18; and increase urinary adenine contents and promote its excretion. In addition, B4 also upregulated the expression of podocin and nephrin, two major podocyte proteins, and reduced the fiber collagen in the renal interstitial, suggesting that B4 could protect the glomerular matrix from adenine injury in addition to its anti-inflammatory effects. The results of this study show new perspective of B4 as a potential drug against adenine-induced renal injury.

1. Introduction

Pulsatilla chinensis (Bge.) Reg (Pulsatilla) is commonly used in traditional Chinese medicine and has antimicrobial and anti-inflammatory functions [14]. Saponins are major ingredients in Pulsatilla [58]; for example, anemoside B4 (B4), which is isolated from the radix of Pulsatilla, has a content of 4% [9, 10]. Referring to the pharmacological studies on B4 in the latest five years mainly includes the detection of pharmacokinetics, tissue distribution, excretion by LC-MS /MS method, and biotransformation and metabolic profile of anemoside B4 in rat small and large intestine microflora [1113]. Relevant studies have shown that B4 has antiviral and immunoregulatory effects in vitro and in viv; B4 could reduce the incidence and severity of porcine circovirus 2 PCV2-induced immunopathological damage, improving the phenomenon of body temperature elevation, weight loss, anaemia, and internal organ swelling, and affect the immunoglobulin levels and protein absorption [14]. B4 might effectively regulate immune responses via upregulated IL-2 expression levels after endothelial cells were challenged with PRRSV [15]. Moreover, B4 has both anti-inflammatory and anticancer effects [1621]. It has certain cytotoxicity on the human myelogenous leukemia K562 cell line and its metabolites could exhibit a reduction in cell viability of SMMC-7721. In a preliminary study, we found that B4 could protect the kidney from injury induced by a variety factors in mice. Thus, we speculated on its protective effects against renal damage.

Most kidney injury is caused by multiple causes and progressive deterioration, resulting in high levels of nephron destruction, irreversible damage to the renal parenchyma, and the subsequent deterioration of renal function. There are clinical manifestations of metabolite retention, including water, electrolyte, acid-base balance, and systemic involvement [22]. During this pathological process, there are also various associated inflammatory factors, such as TNFα and IL-6 [2325]. Excessive adenine cannot be excreted from the kidney in a timely manner, which could lead to crystal formation and kidney microinflammation, resulting in severe kidney injury [26]. Therefore, adenine is a common agent for inducing chronic renal injury [27], as it interferes with the body's normal adenine metabolism, leading to metabolic disorders. Xanthine oxidase in corroboration with 2,8-dihydroxyadenine, an adenine metabolite that is very difficult to dissolve in water and is often deposited in the renal tubules, causes renal tubular obstruction, which leads to a significant increase in serum uric acid, creatinine (Crea) and urea nitrogen (BUN) [28].

To explore the pharmacological actions of B4, we evaluated the effects of B4 on rat renal injury induced by overloaded adenine in this work. We observed changes in the renal pathology and elucidated the mechanism associated with the actions of B4.

2. Materials and Methods

2.1. Animals

Male Wistar rats weighing 160g-180g were purchased from Hunan SJA Laboratory Animal Co., Ltd., Changsha, China. This experiment was completed at the Laboratory of Barrier Environment of the Jiangxi Bencao-Tiangong Technology Co., Ltd. (Nanchang, China). The animals were housed in temperature- and humidity-controlled rooms under a 12 h light/dark cycle and provided with unrestricted amounts of rodent chow and drinkable water. All procedures described were reviewed and approved by the Institutional Animal Care & Use Committee of Jiangxi University of Traditional Chinese Medicine (TCM) and the Animal Welfare & Ethics Committee of Jiangxi University of TCM (approval ID: 17-JunLi-B4). The experimental procedure strictly followed the guidelines of the Experimental Animal Welfare and Ethics of China.

2.2. Chemical and Materials

Anemoside B4 (B4), whose chemical structure is shown in Figure 1(a) (Batch No. 20161107, purity of 98% using HPLC determination, the chromatogram of anemoside B4 is shown in Figure 1(b)) was presented by Professor Yu-Lin Feng from the Phytochemical Department of our university. Prednisolone (pred.) (11-beta,17-alpha; 11,17,21-trihydroxypregna-1,4-diene-3,20-dione; (11beta)-11,17-dihydroxy- 3,20- dioxopregna-1,4-dien-21-yl acetate) (Batch No. 161165) was purchased from Xianju Pharmaceutical Ltd. (Zhejiang, China). Adenine (Sigma-Aldrich, Lot#WXBB0585V) was purchased from Sigma (Shanghai, China). Creatinine (Crea), urea nitrogen (BUN), and total protein (TP) kits were purchased from Heguan Chemical Company (Beijing, China). The Bradford Protein Assay Kit (P0006) was purchased from Beyotime Biotechnology Company (Beijing, China). The qPCR detection kit (Lot# L20509) was purchased from Quanshijin BioChem Tech Ltd. (Beijing, China). Hematoxylin (MHS16-500ML, LOT#SLBK4909V) and Eosin Y (HT110116-500ML, LOT#J6425V) were purchased from Sigma (Shanghai, China). Masson’s trichrome kits (Lot:0606A18) were purchased from Leagene Biotechnology Co., Ltd. (Beijing, China). A Bio-Rad electrophoresis unit and Bio-Rad ChemiDocXRS+ Gel Imaging System (Beijing, China), LEICA RM2235 paraffin slicer, and LEICA DM2500 Optical Microscope (Beijing, China) were used in this study.

2.3. Dosages and Groups

All rats were randomly separated into the following six groups (each group consisting of 10 rats, n=10): the normal control group, model control group, positive control groups, B4 large dose group (2.5 mg/kg), B4 medium dose group (1.25 mg/kg), and B4 small dose group (0.625 mg/kg). All the B4 dosages were determined by the preexperiment, and B4 was given by intravenous administration. Prednisolone, a type of glucocorticoid, was used as positive control (5mg/kg) by oral administration.

2.4. Experimental Process

The chronic kidney disease model was referenced in the Ali and Diwan reports [29, 30]. The rat model was created by oral administration of adenine (mixture with 0.5% CMC-Na solution, 220 mg/kg) for 3 weeks. At day 14 after adenine administration, three dosages of B4 were given by intravenous injection continuously for 4 weeks (one time per day) (the schematic protocol is shown in Figure 1(c)). The normal control was given vehicle with 0.5% CMC-Na solution, the model control was given normal saline, and the positive control was given prednisolone. After 4 weeks of administration, the blood and urine samples were collected, and the rats were killed with anesthesia. The rat kidneys were isolated; the right kidney was fixed with 10% formalin and left kidney was stored at -80°C for protein expression analysis.

During the experiment, the general manifestations of the rats, such as their spirit, motor action, and rat fire light and color, were observed and recorded. Additionally, their body weights were detected and recorded each week. Rat urine was collected each week using metabolite cages. The quantity of urine collected in 24 h was determined, and the urine protein content was tested. Serum was isolated from the rat blood for the biochemical tests. The serum BUN, Crea, and TP were tested using a 7100 automatic biochemical analyzer (Hitachi, Japan). The kidney tissue treated with 10% formalin was analyzed by H.E. preparation or by staining the tissue with picrosirius red and Masson’s trichrome and making observations with a microscope. Grayscale scanning of the images was carried out by using Adobe PhotoshopCS3 (Adobe, California, USA).

2.5. Protein Expression

Protein expression was analyzed using Western blotting as previously described [31, 32]. For Western blot analysis, primary antibodies against NFκB (rabbit polyclonal antibody, ab16502), TNFα (rabbit polyclonal antibody, ab6671), NLRP3 (rabbit polyclonal antibody, ab210491), IL-1β (rabbit polyclonal antibody, ab9722), IL-6 (mouse monoclonal antibody, ab9324), Caspase 1 (rabbit polyclonal antibody, ab1872), and nephrin (rabbit monoclonal antibody, ab216341) were purchased from Abcam (Shanghai, China). TLR4 (mouse monoclonal antibody, sc-293072) and ASC (mouse monoclonal antibody, sc-271054) antibodies were purchased from Santa Cruz (Beijing, China). The IL-18 (rabbit polyclonal antibody, TA324190) and podocin (rabbit polyclonal antibody, TA351459) antibodies were purchased from ORIGENE (Shanghai, China). The goat anti-mouse IgG-HRP (ZB2305) and goat anti-rabbit (ZB2301) IgG-HRP secondary antibodies were purchased from ZSGB-Bio (Shanghai, China). The targeted proteins were visualized with the Super Signal West Femto Chemiluminescent Substrate (Thermo Scientific Pierce, Beijing, China), and the intensities of the visualized bands were analyzed using the Quantity One software (Bio-Rad, Shanghai, China). β-actin (mouse monoclonal antibody, TA-09, Zhongshan Jinqiao Biotech company, Beijing, China) was used as an internal control. The data were expressed as the ratio to β-actin.

2.6. Detection of Adenine Using LC/MS

Quantitative determination was performed using a Rapid Resolution Liquid Chromatography System (1290 Infinity, Agilent) coupled to a triple quadrupole mass spectrometer (6460, Agilent) [33]. The liquid chromatography system was equipped with a binary pump, a thermostatic column compartment, an autosampler, and an ultraviolet diode-array detector.

Chromatographic separation was achieved on a Welch Ultimate Luna 3μm HILIC 200A (2.0×150mm). The mobile phase was a mixture of 0.1% formic acid in water (A) and acetonitrile (B). The gradient elution was programmed as follows: 95% B,0.01-2 min; 95-80% B,2-3 min; 80-70% B,3-4.5 min; 60-95 % B,5.5- 6 min; and 95% B,6.0-7.0 min. The total run time was 7 min. The column temperature was maintained at 30°C and the injection volume was 2μL. The flow rate was set at 0.25 mL/min. The electrospray ionization (ESI) was performed in positive mode. The mass spectrometer parameters were optimized as follows: drying gas flow rate, 9 L/min; drying gas temperature, 325°C; nebulizer pressure, 45 psi; and capillary voltage, 3000 V. Nitrogen was used in all cases. The precursor product ion pairs used in MRM mode were m/z 136.1-119.5 for epinephrine. The fragmentor was set at 100 V and the collision energy (CE) was set at 23 eV. The dwell time of each ion pair was 100 ms. Instrument control, data acquisition, and evaluation were performed with the Mass Hunter workstation software (Version B.04.00).

2.7. Data Analysis

The data were expressed as the mean ± SEM and statistically analyzed using one-way ANOVA analysis, and the t-t test was performed for two groups. The testing was performed using the SPSS 19.0 software (IBM, Chicago, USA). P values less than 0.05 were considered statistically significant. The statistical graphs were produced using the GraphPad Prism 5.0 software (GraphPad Company, San Diego, California, USA) or the Microsoft Office Excel 2010 software (Microsoft, Maryland, USA).

3. Results

3.1. Effect of B4 on the General Conditions and Body Weights of the Rats with Adenine-Induced Renal Injuries

After adenine administration, rats in each group showed signs of apathy, coarse and messy fur, weight loss, and decreased activity. After B4 intervention, these phenomena were improved. The rats’ body weights are displayed in Figures 1(d) and 1(e). Their weights were obviously reduced, implying that the adenine model could influence body weight. B4 at the large and medium doses could reverse the decrease in weight. The small B4 dose had no effect on weight. Prednisolone could not inhibit the decrease in body weight.

3.2. Effect of B4 on Serum Biochemical Indexes in Rats with Adenine-Induced Renal Damage

Figure 2 presents the rats’ kidney functions after the intravenous administration of B4. First, adenine could injure the rat kidney, causing a distinct increase in BUN and Crea. B4 at the large and medium doses could suppress the increase in BUN and Crea compared with the model groups after 2 weeks of B4 administration. Based on Figures 2(a), 2(b), and 2(c), we found that BUN and Crea could decrease with time, reflecting kidney self-recovery. The AUCs (area under the curve) of BUN and Crea were calculated to evaluate the effect of B4 on BUN and Crea, respectively. The AUCs of BUN and Crea in the rat model increased compared with those of the control groups, indicating that adenine actually injured the rat kidneys. B4 at the large and medium doses could also decrease the BUN and Crea AUCs, which is in agreement with the BUN and Crea levels at week 2 (Figures 2(h) and 2(i)). The small B4 dose had no effects. Prednisolone could decrease BUN and Crea similar to B4. However, during all the experiments, the blood total protein (TP) displayed negative changes compared with the control groups (Figures 2(a), 2(d), and 2(g)).

3.3. Effects of B4 on 24 h Urinary Protein Excretion in Rats within Adenine-Induced Renal Injury

Urinary protein is a key index reflecting kidney injury. After adenine overload, the urinary protein levels in the model group were higher than those in the control group, and the total urinary protein at 24 h after 4 weeks was also higher than that of the control group (Figure 3). B4 at the large and small doses could reduce the 24h total protein levels, implying that B4 protects the kidney from adenine injury (Figure 3(d)). After 4 weeks of B4 treatment, there was more urine from the model group at 24 h, and there were no differences in the protein concentrations in model groups; however, the model groups were higher than the normal groups (Figures 3(e) and 3(f)). Finally, the total protein in the B4-treated rat was lower than in the model rat, showing that B4 affects kidney damage by decreasing urinary protein levels.

3.4. Effects of B4 on the Renal Histopathology of Rats with Adenine-Induced Renal Injury

With respect to morphology, the kidney structure of the normal group rats was clear and showed normal glomeruli (renal body), renal tubules, and interstitium. In contrast, the number of nephrons in the model control group decreased, and granulomas were present in the renal interstitium (mainly consisting of macrophage-like lesions). Visible brown adenine crystals were observed in the lumen and interstitium of the renal tubules, and the renal tubules expanded in a reticular pattern and partially disappeared, indicating that adenine could damage the kidney renal tubules (Figure 4). The renal tubule dilation was alleviated in the B4 high- and low-dose groups.

In the model groups, adenine crystallized, implying that the kidney could not handle the adenine overload, and resulted in injury to the kidney tubules. B4 could protect the kidney from the damage caused by the adenine by reducing the number of adenine crystals (Figure 4(a)). To determine the exact adenine contents in the kidney, LC/MS was employed for adenine detection (Figures 4(b)–4(d)). A standard curve was constructed, and the following correlation equation was determined to calculate the adenine concentration: y=326.13x+237.46 (R2=1). After adenine overload, the concentration of adenine in the rat kidney was distinctly higher than in the normal control rat. B4 at the small dose and prednisolone could decrease the adenine levels, but the results were not statistically significant (Figure 4(e)). Interestingly, the adenine contents in rat urine from the groups treated with the middle and small B4 doses were higher than those from the model groups, implying that B4 could promote the secretion of adenine in the urine (Figure 4(f)). To confirm this result, we examined the ratio of adenine in the kidney to adenine in urine (adenine in kidney/adenine in urine). In accordance with the adenine contents, this ratio was lower in the middle and small B4 dose groups than in the model groups, and the results were statistically significant, showing that there were higher adenine levels in urine from the B4 groups than in the model groups (Figure 4(g)). The positive control prednisolone displayed increased adenine levels in urine, but the results were not statistically significant.

3.5. Effect of B4 on the Expression of Inflammatory-Related Factors in the Renal Tissue

In Figure 5, we found that, in addition to adenine overload, the inflammatory cytokines were dramatically upregulated compared with normal control rats, except TLR4. B4 could suppress the expression of IL-6, IL-1β, and NFκB but had a negative effect on TNFα expression, indicating that the anti-inflammatory effects of B4 on adenine-induced kidney damage are related to IL-6 and IL-1β/NFκB signaling. A recent study showed that adenine crystals stored in the tubules caused localized inflammasome expression, which resulted in kidney damage [24]. In our experiments, the expression of NLRP3 and its components were distinctly upregulated by chronic adenine stimulation. However, B4 could effectively suppress this expression, suggesting that the NLRP3 inflammasome is a major inflammatory pathway after adenine overload. The positive control prednisolone could also attenuate the expression of the NLRP3 inflammasome.

3.6. Effects of B4 on Renal Fiber Collagen

Figures 6(a)–6(g) show the fibrous status of the kidney tissue. Figure 6(a) shows that renal tubulointerstitial fibrosis was less likely in kidneys from normal rats. After adenine overloaded, the rat kidney tissue fibers proliferated significantly. B4 showed a specific inhibition of renal fibrosis, which was evident at the medium dose (Figure 6(e)). The positive control prednisolone showed the ability to promote tubulointerstitial fibrosis (Figure 6(c)), which will require further study. The analytic results by using grayscale scanning present that B4 could attenuate the collagen in the renal tubulointerstitial being consistent with the histological images (Figure 6(g)). The initiation of renal fibrosis is generally thought to be associated with high TGF-β (transforming growth factor-beta) expression [34, 35]; therefore TGF-β1 might play a role in the effect of B4 on suppress renal tubulointerstitial fibers caused by adenine overloaded, which needs to be studied further. Nephrin and podocin are the main factors in podocyte-associated protein expression, and their expression directly affects the permeability of the glomerular matrix membrane, which in turn affects kidney function [36]. B4 may significantly increase the expression of nephrin and podocin in a dose-dependent manner, indicating that the ability of B4 to prevent and treat renal injury is related to the promotion of nephrin and podocin expression and in turn improving glomerular podocytes (Figures 6(h)–6(j)).

4. Discussion

In this study, we observed the pharmacological effects of B4. The results showed that B4 can effectively reduce the increase in BUN and Crea induced by adenine and simultaneously reduce urinary protein levels caused by kidney damage, which are related to the inhibition of inflammatory reactions. Additionally, B4 can also improve renal podocytes by enhancing the expression of podocin and nephrin. It is also interesting that B4 promotes the excretion of the overloaded adenine from the kidney, thereby reducing the renal damage.

Studies have shown that localized microinflammation (microlocation) is common in patients with chronic renal failure (CRF); this further promotes the deterioration associated with kidney disease and the emergence of various complications [37]. The degree of microinflammation has been considered as a reliable indicator of CRF prognosis [38]. Therefore, inflammatory factors, such as IL-6, IL-1β, and TNFα, should be examined when studying renal function impairment [28]. The expression of the NLRP3 inflammasome should also be examined because it is correlated with chronic inflammation. Our results show that renal inflammatory factor expression was significantly increased in adenine-induced rat kidney injury. B4 could significantly inhibit the expression of IL-6, TNFα, and NFκB through this related signaling pathway. However, there were no obvious inhibitory effects on IL-1β, which requires further study. Meanwhile, adenine could increase the expression of the NLRP3 inflammasome. In addition to the NLRP3 inflammasome, B4 also significantly inhibited the expression of other three proteins, Caspase 1, ASC, and IL-18, indicating that B4 has a distinct effect on the pathways related to these two kinds of inflammatory responses.

Based on the morphological observations, adenine mainly damages the renal tubules and causes less glomerular damage. In the model group, renal interstitial hyperplasia and tubular dilatation were observed in the kidneys, and adenine crystals were observed in the renal tubules. Inflammatory hyperplasia could be observed around the crystalline tubules, and the wall of the tube was thickened. B4 could improve this kind of tubular hyperplasia to a certain extent and reduce crystallization. The results of the adenine test in the kidney tissue and its excreted urine revealed that B4 could increase adenine levels in rat urine, suggesting that B4 can promote adenine excretion. Excessive adenine excretion from the body could reduce not only the accumulation of crystals in the renal tubules but also the renal tubular damage and inflammatory reactions caused by these crystals.

It is generally believed that renal damage caused by adenine occurs mainly in the renal tubules [39]. Our results showed that urinary protein levels increased significantly in the model group and that B4 could significantly reduce urinary protein levels. Because the increase in urinary protein levels is mainly due to glomerular basement membrane damage, it is suggested that adenine could also damage the glomerular matrix and that B4 could not only act on the renal tubules but also protect the glomerulus from injury.

Glucocorticoids are commonly used drugs in the treatment of acute and chronic kidney injury [40]. Therefore, prednisolone, an active glucocorticoid metabolite, was employed as a positive control in this study [41]. The results showed that prednisolone had a specific effect on adenine-induced renal injury by inhibiting the expression of inflammatory factors and improving renal function. Prednisolone reduced urinary protein levels but had no effect on urinary adenine excretion. Additionally, prednisolone did not improve body weight loss during adenine-induced kidney damage, while B4 could increase rat body weights during adenine overload. In particular, the increase in body weight was significant and statistically significant compared with the model group at the large and medium B4 doses. In addition to its anti-inflammatory role, B4 could also reduce urinary protein levels and accelerate the excretion of adenine.

During this pathological process, podocin and nephrin were significantly downregulated in the model group, while B4 could significantly upregulate their expression, indicating that the protective effects of B4 in the kidney involve protection of the glomerular basement membrane and maintenance of normal podocyte physiological state. Prednisolone had no significant effects on podocin and nephrin expression, implying that the role of this hormone may be mainly to inhibit the expression of inflammatory factors but not to improve the function of the basement membrane, which may be one of the most important differences between prednisolone and B4. B4 can not only inhibit the expression of inflammatory factors but also upregulate the expression of nephrin and podocin and the podocyte function-related proteins, thereby protecting the glomerular basement membrane from damage induced by adenine.

Adenine causes renal tubulointerstitial fibrosis [27, 42, 43], which was also confirmed in our experiments. Our results showed that there was significant fibrosis in the renal tubulointerstitial 6 weeks after adenine overloaded. B4 can inhibit renal interstitial fibrosis distinctly. The mechanism for the B4 inhibition of renal fibrosis caused by adenine remains to be further studied.

Taken together, B4 may be effective for treating chronic kidney injury (CKI) induced by adenine. The mechanism of B4 in CKI is correlated with decreasing BUN, Crea, and urinary protein levels; protecting glomeruli; promoting adenine excretion; and inhibiting the expression of inflammatory factors, thereby attenuating renal tubular injury. Additionally, B4 can also upregulate the expression of nephrin and podocin, preventing the glomeruli from injury induced by adenine.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Qin Gong and Lu-Ling He equally contributed to this work.

Acknowledgments

We thank all the colleagues in our laboratory for the assistance of the article. This work was supported by National Innovative Drugs 13th Five-Year Major Special Project of China (2018ZX09301030-002).

References

  1. W.-H. Wang, J. Yang, H.-S. Peng, and J.-P. Qian, “Study on morphological characteristics and microscopic structure of medicinal organs of pulsatilla chinensis (Bunge) regel,” Microscopy Research and Technique, vol. 80, no. 8, pp. 950–958, 2017. View at: Publisher Site | Google Scholar
  2. Y. Shi, M. Zhao, H. Yao et al., “Rapidly discriminate commercial medicinal Pulsatilla chinensis (Bge.) regel from its adulterants using ITS2 barcoding and specific PCR-RFLP assay,” Scientific Reports, vol. 7, Article ID e40000, 2017. View at: Google Scholar
  3. L.-D. Li, W.-C. Li, C.-W. Liu et al., “Giardia intestinalis: effects of pulsatilla chinensis extracts on trophozoites,” Parasitology Research, vol. 111, no. 5, pp. 1929–1935, 2012. View at: Publisher Site | Google Scholar
  4. F. Zhou, O. Lv, Y. Zheng et al., “Inhibitory effect of Pulsatilla chinensis polysaccharides on glioma,” International Journal of Biological Macromolecules, vol. 50, no. 5, pp. 1322–1326, 2012. View at: Publisher Site | Google Scholar
  5. Y. Mimaki, A. Yokosuka, M. Kuroda, M. Hamanaka, C. Sakuma, and Y. Sashida, “New bisdesmosidic triterpene saponins from the roots of Pulsatilla chinensis,” Journal of Natural Products, vol. 64, no. 9, pp. 1226–1229, 2001. View at: Publisher Site | Google Scholar
  6. L. I. Glebko, N. P. Krasovskaj, L. I. Strigina, K. P. Ulanova, V. A. Denisenko, and P. S. Dmitrenok, “Triterpene glycosides from Pulsatilla chinensis,” Russian Chemical Bulletin, vol. 51, no. 10, pp. 1945–1950, 2002. View at: Publisher Site | Google Scholar
  7. M.-M. Jin, W.-D. Zhang, Y.-M. Xu et al., “Simultaneous determination of 12 active components in the roots of Pulsatilla chinensis using tissue-smashing extraction with liquid chromatography and mass spectrometry,” Journal of Separation Science, vol. 40, no. 6, pp. 1283–1292, 2017. View at: Publisher Site | Google Scholar
  8. K. Xu, Z. Shu, Q.-M. Xu et al., “Cytotoxic activity of Pulsatilla chinensis saponins and their structure-activity relationship,” Journal of Asian Natural Products Research, vol. 15, no. 6, pp. 680–686, 2013. View at: Publisher Site | Google Scholar
  9. Y. Ling, Z. Lin, W. Zha, T. Lian, and S. You, “Rapid detection and characterisation of triterpene saponins from the root of pulsatilla chinensis (Bunge) Regel by HPLC-ESI-QTOF-MS/MS,” Phytochemical Analysis, pp. 174–183, 2016. View at: Publisher Site | Google Scholar
  10. L. Wang, Q. Xu, S. Su et al., “Simultaneous purification of pulchinenoside B4 and B5 from pulsatilla chinensis using macroporous resin and preparative high performance liquid chromatography,” Industrial & Engineering Chemistry Research, vol. 51, no. 45, pp. 14859–14866, 2012. View at: Publisher Site | Google Scholar
  11. L. Yang, X. Meng, X. Yu, and H. Kuang, “Simultaneous determination of anemoside B4, phellodendrine, berberine, palmatine, obakunone, esculin, esculetin in rat plasma by UPLC–ESI–MS/MS and its application to a comparative pharmacokinetic study in normal and ulcerative colitis rats,” Journal of Pharmaceutical and Biomedical Analysis, vol. 134, pp. 43–52, 2017. View at: Publisher Site | Google Scholar
  12. X. Guo, Y. Xie, S. Lian et al., “A sensitive HPLC–MS/MS method for the simultaneous determination of anemoside B4, anemoside A3 and 23-hydroxybetulinic acid: application to the pharmacokinetics and liver distribution of Pulsatilla chinensis saponins,” Biomedical Chromatography, vol. 32, no. 3, Article ID e4124, 2018. View at: Publisher Site | Google Scholar
  13. M. He, H. Ouyang, M. He et al., “Application of a liquid chromatography–tandem mass spectrometry method to the application of a liquid chromatography–tandem mass spectrometry method to the pharmacokinetics, tissue distribution and excretion in the study of anemoside B4, a novel antiviral agent candidate, in rats,” Biomedical Chromatography, vol. 31, no. 7, Article ID e3914, 2017. View at: Publisher Site | Google Scholar
  14. H. Yang, X. Chen, C. Jiang, K. He, and Y. Hu, “Antiviral and immunoregulatory role against PCV2 in vivo of Chinese herbal medicinal ingredients,” Journal of Veterinary Research (Poland), vol. 61, no. 4, pp. 405–410, 2017. View at: Publisher Site | Google Scholar
  15. Y. Hu, A. Mao, Y. Tan, Y. Zhao, and K. He, “Role of 5 saponins in secretion of cytokines by PRRSV-induced endothelial cells,” Drug Research, vol. 66, no. 7, pp. 357–362, 2016. View at: Publisher Site | Google Scholar
  16. M. Liu, X. Zhao, L. Xiao et al., “Cytotoxicity of the compounds isolated from Pulsatilla chinensis saponins and apoptosis induced by 23-hydroxybetulinic acid,” Pharmaceutical Biology, vol. 53, no. 1, pp. 1–9, 2015. View at: Publisher Site | Google Scholar
  17. Y.-Y. Luo, L.-Y. Chen, H. Jian et al., “Regulation of saponins from Pulsatilla chinensis on energy metabolism of Bel-7402 xenograft in nude mice,” Chinese Traditional and Herbal Drugs, vol. 45, no. 7, pp. 973–977, 2014. View at: Google Scholar
  18. T. Liu, L. Ye, X. Guan et al., “Immunopontentiating and antitumor activities of a polysaccharide from Pulsatilla chinensis (Bunge) Regel,” International Journal of Biological Macromolecules, vol. 54, no. 1, pp. 225–229, 2013. View at: Publisher Site | Google Scholar
  19. Q.-M. Xu, Z. Shu, W.-J. He et al., “Antitumor activity of Pulsatilla chinensis (Bunge) Regel saponins in human liver tumor 7402 cells in vitro and in vivo,” Phytomedicine, vol. 19, no. 3-4, pp. 293–300, 2012. View at: Publisher Site | Google Scholar
  20. Y. Mimaki, M. Kuroda, T. Asano, and Y. Sashida, “Triterpene saponins and lignans from the roots of Pulsatilla chinensis and their cytotoxic activity against HL-60 cells,” Journal of Natural Products, vol. 62, no. 9, pp. 1279–1283, 1999. View at: Publisher Site | Google Scholar
  21. J. Y. Wan, Y. Z. Zhang, J. B. Yuan et al., “Biotransformation and metabolic profile of Anemoside B4 with rat small and large intestine microflora by ultra-high performance liquid chromatography-quadrupole time of flight tandem mass spectrometry,” Biomedical Chromatography, 2016. View at: Google Scholar
  22. M. Al Za'abi, A. Shalaby, P. Manoj, and B. H. Ali, “The in vivo effects of adenine-induced chronic kidney disease on some renal and hepatic function and CYP450 metabolizing enzymes,” Physiological Research, vol. 66, no. 2, pp. 263–271, 2017. View at: Google Scholar
  23. H. L. Runolfsdottir, R. Palsson, I. M. Agustsdottir, O. S. Indridason, and V. O. Edvardsson, “Kidney disease in adenine phosphoribosyltransferase deficiency,” American Journal of Kidney Diseases, vol. 67, no. 3, pp. 431–438, 2016. View at: Publisher Site | Google Scholar
  24. O. Akchurin, A. Sureshbabu, S. B. Doty et al., “Lack of hepcidin ameliorates anemia and improves growth in an adenine-induced mouse model of chronic kidney disease,” American Journal of Physiology-Renal Physiology, vol. 311, no. 5, pp. F877–F889, 2016. View at: Publisher Site | Google Scholar
  25. M. Correa-Costa, T. T. Braga, R. J. F. Felizardo et al., “Macrophage trafficking as key mediator of adenine-induced kidney injury,” Mediators of Inflammation, vol. 2014, Article ID e291024, 12 pages, 2014. View at: Publisher Site | Google Scholar
  26. S. L. Chong and Y. H. Ng, “Obstructive uropathy and severe acute kidney injury from renal calculi due to adenine phosphoribosyltransferase deficiency,” World Journal of Pediatrics, vol. 12, no. 2, pp. 243–245, 2016. View at: Publisher Site | Google Scholar
  27. V. Diwan, L. Brown, and G. C. Gobe, “Adenine-induced chronic kidney disease in rats,” Nephrology, vol. 23, no. 1, pp. 5–11, 2018. View at: Publisher Site | Google Scholar
  28. B. S. Franklin, M. S. Mangan, and E. Latz, “Crystal formation in inflammation,” Annual Review of Immunology, vol. 34, pp. 173–202, 2016. View at: Publisher Site | Google Scholar
  29. B. H. Ali, L. Cahliková, L. Opletal et al., “Effect of aqueous extract and anthocyanins of calyces of Hibiscus sabdariffa (Malvaceae) in rats with adenine-induced chronic kidney disease,” Journal of Pharmacy and Pharmacology, vol. 69, no. 9, pp. 1219–1229, 2017. View at: Publisher Site | Google Scholar
  30. V. Diwan, G. Gobe, and L. Brown, “Glibenclamide improves kidney and heart structure and function in the adenine-diet model of chronic kidney disease,” Pharmacological Research, vol. 79, pp. 104–110, 2014. View at: Publisher Site | Google Scholar
  31. X. Wang, X. Yu, X. Yan et al., “TRPM8 in the negative regulation of TNFα expression during cold stress,” Scientific Reports, vol. 7, no. 1, Article ID e45155, 2017. View at: Publisher Site | Google Scholar
  32. Z. Yuan, X. Lu, F. Lei et al., “TATA boxes in gene transcription and poly(A) tails in mRNA stability: new perspective on the effects of berberine,” Scientific Reports, vol. 5, no. 1, Article ID e18326, 2016. View at: Publisher Site | Google Scholar
  33. J. Shi, H.-F. Liu, J. M. Wong, R. N. Huang, E. Jones, and T. J. Carlson, “Development of a robust and sensitive LC-MS/MS method for the determination of adenine in plasma of different species and its application to in vivo studies,” Journal of Pharmaceutical and Biomedical Analysis, vol. 56, no. 4, pp. 778–784, 2011. View at: Publisher Site | Google Scholar
  34. Y.-Y. Zhao, X.-L. Cheng, F. Wei et al., “Intrarenal metabolomic investigation of chronic kidney disease and its TGF-β1 mechanism in induced-adenine rats using UPLC Q-TOF/HSMS/MSE,” Journal of Proteome Research, vol. 12, no. 2, pp. 692–703, 2013. View at: Publisher Site | Google Scholar
  35. P. Wang, M. L. Luo, E. Song et al., “Long noncoding RNA lnc-TSI inhibits renal fibrogenesis by negatively regulating the TGF-/Smad3 pathway,” Science Translational Medicine, vol. 10, p. e2039, 2018. View at: Publisher Site | Google Scholar
  36. A. Tofighi, S. Ahmadi, S. M. Seyyedi, A. Shirpoor, F. Kheradmand, and F. H. Gharalari, “Nandrolone administration with or without strenuous exercise promotes overexpression of nephrin and podocin genes and induces structural and functional alterations in the kidneys of rats,” Toxicology Letters, vol. 282, pp. 147–153, 2018. View at: Publisher Site | Google Scholar
  37. S. Cottone, M. C. Lorito, R. Riccobene et al., “Oxidative stress, inflammation and cardiovascular disease in chronic renal failure,” Journal of Nephrology, vol. 21, no. 2, pp. 175–179, 2008. View at: Google Scholar
  38. E. Avci, E. Çakir, S. C. Cevher, H. Yaman, M. Agilli, and C. Bilgi, “Determination of oxidative stress and cellular inflammation in patients with diabetic nephropathy and non-diabetic nephropathy being administered hemodialysis treatment due to chronic renal failure,” Renal Failure, vol. 36, no. 5, pp. 767–773, 2014. View at: Publisher Site | Google Scholar
  39. D. Claramunt, H. Gil-Peña, R. Fuente et al., “Chronic kidney disease induced by adenine: a suitable model of growth retardation in uremia,” American Journal of Physiology-Renal Physiology, vol. 309, no. 1, pp. F57–F62, 2015. View at: Publisher Site | Google Scholar
  40. T. Hamano, N. Fujii, Y. Nagasawa et al., “Serum NTX is a practical marker for assessing antiresorptive therapy for glucocorticoid treated patients with chronic kidney disease,” Bone, vol. 39, no. 5, pp. 1067–1072, 2006. View at: Publisher Site | Google Scholar
  41. R. Rebolledo, B. Liu, M. Z. Akhtar et al., “Prednisolone has a positive effect on the kidney but not on the liver of brain dead rats: a potencial role in complement activation,” Journal of Translational Medicine, vol. 12, no. 1, article e111, 2014. View at: Publisher Site | Google Scholar
  42. V. Diwan, L. Brown, and G. C. Gobe, “The flavonoid rutin improves kidney and heart structure and function in an adenine-induced rat model of chronic kidney disease,” Journal of Functional Foods, vol. 33, pp. 85–93, 2017. View at: Publisher Site | Google Scholar
  43. R. Thakur, A. Sharma, M. C. Lingaraju et al., “Ameliorative effect of ursolic acid on renal fibrosis in adenine-induced chronic kidney disease in rats,” Biomedicine & Pharmacotherapy, vol. 101, pp. 972–980, 2018. View at: Publisher Site | Google Scholar

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