Involvement of the NF-κB signaling pathway in the renoprotective effects of isorhamnetin in a type 2 diabetic rat model
- Authors:
- Published online on: March 22, 2016 https://doi.org/10.3892/br.2016.636
- Pages: 628-634
Abstract
Introduction
As a leading cause of clinical end-stage renal disease, diabetic nephropathy (DN) is the second most prevalent diabetes-associated complication (1). A number of factors are associated with the pathogenesis of DN. However, the exact mechanisms have not been well elucidated. Therefore, no specific therapies have been developed.
Accumulating evidence indicates that inflammation is one of the major factors that has significant roles in the initiation and progression of DN (2–4). The activation of the nuclear factor-κB (NF-κB) signaling pathway has been suggested to be associated with DN (5–7). The roles of the downstream inflammatory mediators of the NF-κB signaling pathway, such as tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), IL-6, intercellular adhesion molecule-1 (ICAM-1) and transforming growth factor-β1 (TGF-β1), have been well demonstrated (8–10). They can promote the glomerular hypertrophy, expansion of the mesangial matrix and thickening of the glomerular and tubular basement membranes, ultimately resulting in proteinuria, glomerulosclerosis and tubulointerstitial fibrosis.
Excessive production of reactive oxygen species has been found in diabetic animals and patients (11). Recently, studies have demonstrated that oxidative stress is an important pathogenic factor of diabetic complications including nephropathy (12–14). Oxidative stress and inflammation are linked, as each begets and amplifies the other. NF-κB has an important role between the interaction of oxidative stress and inflammation.
Considering the crucial roles of inflammation and oxidative stress in the pathogenesis of DN, antioxidant therapy and anti-inflammation therapy have been tested in DN. Cumulative evidence suggests that these managements can preserve renal function and prevent or slow the progression of DN (15–17). Isorhamnetin (ISO) is a plant flavonoid abundant in herbal medicinal plants, such as Hippophae rhamnoides L. In recent studies, ISO exhibited strong antioxidant and anti-inflammatory properties. Its protective effects on lipopolysaccharide (LPS)-induced acute lung injury in mice (18), apoptosis in TNF-α-induced HUVECs injury (19) and chemically-induced inflammatory bowel disease (20) have been reported. A previous study showed that ISO could negatively regulate the NF-κB signaling cascade in gastric cancer (21). However, its effects on kidney function, the NF-κB signaling pathway, inflammatory response and oxidative stress in diabetic subjects have not been evaluated. Therefore, the present study was designed to test the hypothesis that ISO presents renoprotective effects in type 2 diabetic rats and to detect its possible mechanisms.
Materials and methods
Animals
Sprague-Dawley rats (8 weeks old and 180–220 g) obtained from the SLAC Lab Animal Center (Shanghai, China) were used in this study. Procedures used in the current study were approved by the Ethics Committee of Affiliated Hospital of Weifang Medical College (Weifang, Shandong, China). Animals were housed 5/cage in a controlled environment (22±1°C, 12-h light/dark cycle).
Induction of diabetes in rats
Type 2 diabetes mellitus (DM) was induced according to the method described in the literature (22). Rats were fed a high-fat diet consisting of a total kcal value of 40 kJ/kg (22% protein, 20% fat and 45% carbohydrate). A single dose of streptozocin (STZ) [freshly diluted with 0.01 M citrate buffer, (pH 4.5), 30 mg/kg] was intraperitoneally injected into the rats after 4 weeks of the high-fat diet. On day 7 post-STZ injection, blood glucose was measured using the OneTouch®Ultra machine (LifeScan, Livingstone, UK). Rats with hyperglycemia (>16.7 mmol/l) were considered to be diabetic and were included for further study. Normal control rats were fed a regular chow diet with a total kcalories value of 20 kJ/kg (20% protein, 5% fat and 52% carbohydrate) without STZ injection.
Experimental groups and ISO treatment
The diabetic rats were randomly divided into 3 groups (n=10 in each group): DM, 50 mg/kg ISO (ISO-50) and 150 mg/kg ISO (ISO-150) groups. Rats in the ISO-50 and ISO-150 groups were orally administered ISO (50 and 150 mg/kg/day, respectively) after grouping for consecutive 12 weeks. Rats in the control group (n=10 in each group) and the DM group were orally administrated with the same volume of saline.
Preparation of renal homogenate and urine
On the last day of ISO treatment, the rats were placed in metabolic cages and 24-h urine was collected. The kidney was removed and rinsed with ice-cold saline. A section of kidney tissue was homogenized (100 mg renal tissue/ml saline) and centrifuged at 1,050 × g for 10 min. The supernatant was collected and further centrifuged at 10,000 × g for 10 min.
Measurements of renal damage biochemical markers and blood glucose
Levels of urinary osteopontin and kidney injury molecule-1 (KIM-1) were measured using ELISA kits according to the instructions provided by the manufacturer (Boster Biological Technology, Ltd., Wuhan, Hubei, China). The levels of urinary albumin were measured using an automatic biochemistry analyzer. Fasting blood glucose (FBG) was measured using OneTouch®Ultra machine.
Cell culture with LPS and ISO
Rat glomerular mesangial cells (GMCs) (Chinese Center for Typical Culture Collection, Wuhan, Hubei, China) were maintained at 5% CO2 and 37°C in Dulbecco's modified Eagle's medium (Wisent Bioproducts, St. Bruno, Quebec, Canada) containing fetal bovine serum, 100 µg/ml streptomycin 100 U/ml penicillin. GMCs were randomly divided into the following 4 groups: Normal control (NC), LPS [with the presence of 10 nmol/ml LPS (Sigma-Aldrich, St. Louis, MO, USA) in the medium], ISO-5 (10 nmol/ml LPS and 5 µM ISO in the medium) and ISO-10 (10 nmol/ml LPS and 10 µM ISO in the medium) groups. The cells in each group were cultured for 72 h and the medium was collected. Cells were lysed with lysis buffer and the supernatants of the cell lysates were collected after centrifugation at 18,000 × g for 10 min at 4°C.
Measurements of NF-κB p65, phospho-NF-κB p65, inhibitor of NF-κB (IκBα) and phospho-IκBα
The levels of NF-κB p65, phospho-NF-κB p65, IκBα and phospho-IκBα in the cell lysate and in the renal homogenate were measured using ELISA kits, according to the manufacturer's protocols. NF-κB p65 ELISA kits were purchased from Cusabio Biotech Co., Ltd. (Wuhan, China), phospho-NF-κB p65 and phospho-IκBα ELISA kits were purchased from Cell Signaling Technology, Inc. (Beverly, MA, USA), and the IκBα ELISA kits were purchased from Jining Co. (Shanghai, China).
NF-κB p65 DNA-binding activity
Nuclear protein was extracted from the kidney and rat GMCs. NF-κB DNA-binding activity was measured using the NF-κB p65 transcription factor ELISA assay kits (Cayman Chemical Co., Ann Arbor, MI, USA) according to the manufacturer's protocol.
Measurements of inflammatory mediators
The levels of the NF-κB downstream inflammatory mediators, TNF-α, IL-1β, IL-6, ICAM-1 and TGF-β1, in the cell culture medium and in the renal homogenate were measured using ELISA kits from R&D Systems, Inc. (Minneapolis, MN, USA) according to the manufacturer's protocol.
mRNA expression levels of NF-κB p65, TNF-α, IL-1β, IL-6, ICAM-1 and TGF-β1
Total RNA was isolated from fresh kidney tissue and GMCs using TRIzol reagents (Invitrogen, Thermo Fisher Scientific, Inc., Waltham, MA, USA). cDNA was synthesized using the cDNA synthesis kit (Takara Bio, Inc., Kyoto, Japan) and amplified by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The primer sequences were: TNF-α forward, 5′-TGATCGGTCCCAACAAGGA-3′ and reverse primer, 5′-TGCTTGGTGGTTTGCTACGA-3′; IL-1β forward, 5′-ACTATGGCAACTGTCCCTGAAC-3′ and reverse primer, 5′-GTGCTTGGGTCCTCATCCTG-3′; IL-6 forward, 5′-AGTTGCCTTCTTGGGACTGA-3′ and reverse primer 5′-CAGAATTGCCATTGCACAAC-3′; NF-κB p65 forward, 5′-TGCAGGCTCCTGTGCGAGTG-3′ and reverse primer, 5′-TCCGGTGGCGATCGTCTGTGT-3′; ICAM-1 forward, 5′-CGTGGCGTCCATTTACACCT-3′ and reverse primer, 5′-TTAGGGCCTCCTCCTGAGC-3′; TGF-β1 forward, TGGCGTTACCTTGGTAACC and reverse primer, GGTGTTGAGCCCTTTCCAG; and β-actin forward, 5′-AGGCCCCTCTGAACCCTAAG-3′ and reverse primer, 5′-CCAGAGGCATACAGGGACAAC-3′. The PCR program involved 95°C for 30 sec and 40 PCR cycles (95°C for 5 sec and 60°C for 30 sec). The PCR reactions were perforemd with an iQ5 Real-Time PCR Detection system (Bio-Rad, Hercules, CA, USA).
Measurements of oxidative stress activity and antioxidant activity
Oxidative stress activity was assessed by measuring the levels of malondialdehyde (MDA) in the cell culture medium and in the renal homogenate using chemichromatometry kits (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). Antioxidant activity was assessed by measuring levels of total superoxide dismutase (T-SOD) using chemichromatometry kits (Nanjing Jiancheng Bioengineering Institute, Nanjing, China).
Statistical analysis
Statistical analyses were carried out using SPSS software 14.0 (SPSS, Inc., Chicago, IL, USA). Data are reported as mean ± standard deviation and were analyzed using one-way analysis of variance followed by Student-Newman-Keuls test for multiple comparisons. For all the tests, P<0.05 was considered to indicate a statistically significant difference.
Results
Effects of ISO on renal damage biochemical markers
The DM group had higher levels of urinary osteopontin, KIM-1 and albumin compared to the control group (P<0.05). The ISO-50 and ISO-150 groups had lower levels of these renal damage markers compared to the DM group (P<0.05), and those levels of the ISO-150 group were lower compared to the ISO-50 group (P<0.05), indicating that ISO dose-dependently improved the renal function in the diabetic rats (Table I).
Effects of ISO on blood glucose
No significant differences in the FBG levels were observed among the DM, the ISO-50 and the ISO-150 groups (P>0.05). All three groups had higher levels of FBG compared to the control group (P<0.05) (Table I).
Effects of ISO on NF-κB p65, phospho-NF-κB p65, IκBα and phospho-IκBα
In the in vivo study, the high-fat diet plus STZ injection activated the renal NF-κB signaling by increasing levels of NF-κB p65 (protein and mRNA), phospho-NF-κB p65 and phospho-IκBα in the DM group when compared to the control group (P<0.05). The NF-κB activation was inhibited by ISO if compared to the DM group (P<0.05), and the inhibitory effects were dose-dependent in the ISO-50 group and the ISO-150 group (P<0.05). In the in vitro study, LPS increased the generation of NF-κB p65 (protein and mRNA), phospho-NF-κB p65 and phospho-IκBα in GMCs when compared to the normal control cells (P<0.05). ISO dose-dependently (5 and 10 µM) inhibited the overproduction of NF-κB p65 (protein and mRNA), phospho-NF-κB p65 and phospho-IκBα if compared to the LPS group (P<0.05). No significant differences in levels IκBα were observed among the groups in the in vivo and in vitro studies (P>0.05) (Tables II and III).
Effects of ISO on NF-κB p65 DNA-binding activity
In the in vivo study, the DM group had a higher NF-κB p65 DNA-binding activity compared to the control group (P<0.05). ISO (50 and 150 mg) dose-dependently decreased the NF-κB p65 DNA-binding activity when compared to the DM group (P<0.05). In the in vitro study, the LPS group showed higher NF-κB p65 DNA-binding activity compared to the normal control cells (P<0.05), and ISO dose-dependently (5 and 10 µM) inhibited the NF-κB p65 DNA-binding activity when compared to the LPS group (P<0.05) (Tables II and III).
Effects of ISO on inflammatory mediators
The changes (protein and mRNA) of TNF-α, IL-1β, IL-6, ICAM-1 and TGF-β1, which are the downstream inflammatory mediators of NF-κB signaling pathway, were investigated. In the in vivo study, there were higher levels of these inflammatory mediators in the DM group compared to the control group (P<0.05). ISO (50 and 150 mg) dose-dependently decreased these inflammatory mediators when compared to the DM group (P<0.05). In the in vitro study, there were higher levels of these inflammatory mediators in the LPS group compared to the normal control cells (P<0.05). ISO (5 and 10 µM) dose-dependently decreased these inflammatory mediators when compared to the LPS group (P<0.05) (Tables IV–VII).
Table VII.Effects of ISO treatment on mRNA expression of inflammatory mediators in the glomerular mesangial cells. |
Effects of ISO on oxidative stress
The levels of MDA and T-SOD were investigated. In the in vivo study, the DM group had higher levels of MDA and lower levels of T-SOD compared to the control group (P<0.05). ISO (50 and 150 mg) dose-dependently reversed the changes of MDA and T-SOD when compared to the DM group (P<0.05). In the in vitro study, the LPS group showed higher levels of MDA and lower levels of T-SOD compared to the normal control cells (P<0.05). ISO (5 and 10 µM) dose-dependently reversed the changes of MDA and T-SOD when compared to the LPS group (P<0.05) (Tables VIII and IX).
Table IX.Effects of ISO treatment on the oxidative stress markers in the glomerular mesangial cells. |
Discussion
The prevalence of DN is rapidly increasing worldwide due to a rise in the prevalence of type 2 DM (23); however, no specific therapies for DN have been developed. Adequate glycemic control is believed to contribute to the decrease of renal vascular damage risks. The renin-angiotensin system blockade with angiotensin-converting-enzyme inhibitor is currently employed as a first-line treatment for DN (24). Angiotensin II type 1 receptor antagonist is also used to slow the progression of DN (25). However, DN still progresses with these drugs, and therefore, more novel agents are required.
ISO is a plant flavonoid abundant in herbal medicinal plants, such as Hippophae rhamnoides L. It has been tested in inflammation-associated diseases (18,20,26) and oxidative stress-associated diseases (27,28). However, to the best of our knowledge, no studies had evaluated its effects on kidney function in DN animals, which is also associated with inflammation and oxidative stress. In the study, a type 2 diabetes model was established in rats fed a high-fat diet and a small dose of STZ, as described previously (22). Levels of urinary osteopontin and KIM-1, which are specific biomarkers of the early-stage renal damage and urinary albumin, were determined to evaluate the renal function damage of the animals. The DM group showed markedly higher levels of urinary osteopontin, KIM-1 and albumin compared to the control group, indicating that the high-fat diet and STZ injection induced significant renal function damage. However, ISO dose-dependently inhibited the increases of the three parameters when compared to the DM group. Therefore, the results of the present analyses indicated that ISO possesses renoprotective effects in type 2 diabetic rats.
Regulation of blood glucose is believed to contribute to a reduced renal risk. The blood glucose levels of the animals were evaluated and the DM and ISO groups had comparable levels of blood glucose. The results indicated that the recovery of renal damage did not benefit from blood glucose reduction.
Among the complex mechanisms leading to DN, inflammation has a key role (2–4). Increased levels of the inflammatory factors are associated with the initiation and progression of DN (8–10,29). Among the inflammatory factors, activated NF-κB can induce inflammatory cascade reactions, ultimately leading to renal damage. The present study showed that the DM group had increased protein and mRNA levels of NF-κB p65 and its active form phospho-NF-κB p65. The result was consistent with previous studies, which found increased NF-κB activity in diabetic animals (5,7,30). IκBα is an inhibitor of the activation of NF-κB p65, which can suppress the phosphorylation of NF-κB p65. However, significant differences were not found in the levels of IκBα among all the groups. As the phosphorylation of IκBα can induce the NF-κB activation, the levels of phospho-IκBα were measured and the DM group had higher levels of phospho-IκBα compared to the control group. Theoretically, the activated NF-κB p65 can be translocated to the nucleus to promote the transcription of the target genes. Consistently, the DM group had higher NF-κB p65 DNA-binding activity compared to the control groups. Furthermore, the investigations of the downstream inflammatory mediators of NF-κB signaling pathway also showed that the DM group had increased protein and mRNA levels of TNF-α, IL-1β, IL-6, ICAM-1 and TGF-β1. The roles of TNF-α, IL-1β, IL-6, ICAM-1 and TGF-β1 in the initiation and progression of DN have been well demonstrated in previous studies (8–10). Controlling the overexpression of these inflammatory mediators has exhibited beneficial effects in DN subjects (17,31). Notably, the present study found that ISO dose-dependently inhibited the increased production of NF-κB p65, phospho-NF-κB p65, phospho-IκBα and inflammatory cytokines, and decreased the NF-κB p65 DNA-binding activity as well when compared to the DM group. The result indicated that ISO could negatively regulate the NF-κB signaling pathway. This was consistent with the studies reporting that ISO inhibited the NF-κB activity in inflammatory disorders (18,20,32) and tumors (21). On the basis of those prior studies and the present data, it is hypothesized that the inhibitory effects on the NF-κB-mediated inflammatory response may be beneficial for the recovery of renal damage.
In addition to mediating an inflammatory response, NF-κB also triggers the oxidative reactions. NF-κB has an important role between the interaction of oxidative stress and inflammation. Oxidative stress is involved in numerous disorders (33). In the present study, the DM group had higher levels of oxidative marker MDA and lower levels of antioxidative marker T-SOD. This was consistent with the studies that reported increased oxidative activity in diabetic subjects (34,35). There is increasing evidence from pre-clinical and clinical studies, which suggests that antioxidant agents have potential ameliorative effects on diabetic complications, including DN (17,36,37). In the present study, ISO dose-dependently inhibited the overgeneration of MDA and increased the T-SOD activity, which suggested antioxidative activity of ISO in diabetic rats. Similarly, certain studies have also reported its antioxidative activity in other disorders (26–28,38). Therefore, the ameliorative effects on renal damage may also benefit from the suppression of oxidative stress.
In order to confirm the anti-inflammatory and antioxidative activity of ISO, rat GMCs were cultured with the presence of LPS or LPS+ISO. LPS is extensively used to induce an inflammatory state in vitro and in vivo (39). The present study showed that rat GMCs with LPS stimulation produced higher levels of NF-κB p65, phospho-NF-κB p65, phospho-IκBα, TNF-α, IL-1β, IL-6, ICAM-1 and TGF-β1, and increased the NF-κB p65 DNA-binding activity and oxidative stress, when compared to the normal control cells. Notably, ISO inhibited the changes induced by LPS stimulation. This was consistent with the in vivo investigations in the present study.
Collectively, ISO had renoprotective effects in type 2 diabetic rats. The recovery of renal damage may be associated with the inhibition of the NF-κB signaling pathway.
References
Si X, Li P, Zhang Y, Zhang Y, Lv W and Qi D: Renoprotective effects of olmesartan medoxomil on diabetic nephropathy in streptozotocin-induced diabetes in rats. Biomed Rep. 2:24–28. 2014.PubMed/NCBI | |
Downs CA and Faulkner MS: Toxic stress, inflammation and symptomatology of chronic complications in diabetes. World J Diabetes. 6:554–565. 2015.PubMed/NCBI | |
Barutta F, Bruno G, Grimaldi S and Gruden G: Inflammation in diabetic nephropathy: Moving toward clinical biomarkers and targets for treatment. Endocrine. 48:730–742. 2015. View Article : Google Scholar : PubMed/NCBI | |
García-García PM, Getino-Melián MA, Domínguez-Pimentel V and Navarro-González JF: Inflammation in diabetic kidney disease. World J Diabetes. 5:431–443. 2014. View Article : Google Scholar : PubMed/NCBI | |
Yi B, Hu X, Zhang H, Huang J, Liu J, Hu J, Li W and Huang L: Nuclear NF-κB p65 in peripheral blood mononuclear cells correlates with urinary MCP-1, RANTES and the severity of type 2 diabetic nephropathy. PLoS One. 9:e996332014. View Article : Google Scholar : PubMed/NCBI | |
Ahad A, Ganai AA, Mujeeb M and Siddiqui WA: Ellagic acid, an NF-κB inhibitor, ameliorates renal function in experimental diabetic nephropathy. Chem Biol Interact. 219:64–75. 2014. View Article : Google Scholar : PubMed/NCBI | |
Yang SM, Ka SM, Wu HL, Yeh YC, Kuo CH, Hua KF, Shi GY, Hung YJ, Hsiao FC, Yang SS, et al: Thrombomodulin domain 1 ameliorates diabetic nephropathy in mice via anti-NF-κB/NLRP3 inflammasome-mediated inflammation, enhancement of NRF2 antioxidant activity and inhibition of apoptosis. Diabetologia. 57:424–434. 2014. View Article : Google Scholar : PubMed/NCBI | |
Ahad A, Ahsan H, Mujeeb M and Siddiqui WA: Gallic acid ameliorates renal functions by inhibiting the activation of p38 MAPK in experimentally induced type 2 diabetic rats and cultured rat proximal tubular epithelial cells. Chem Biol Interact. 240:292–303. 2015. View Article : Google Scholar : PubMed/NCBI | |
Wu JS, Shi R, Lu X, Ma YM and Cheng NN: Combination of active components of Xiexin decoction ameliorates renal fibrosis through the inhibition of NF-κB and TGF-β1/Smad pathways in db/db diabetic mice. PLoS One. 10:e01226612015. View Article : Google Scholar : PubMed/NCBI | |
Gui D, Huang J, Guo Y, Chen J, Chen Y, Xiao W, Liu X and Wang N: Astragaloside IV ameliorates renal injury in streptozotocin-induced diabetic rats through inhibiting NF-κB-mediated inflammatory genes expression. Cytokine. 61:970–977. 2013. View Article : Google Scholar : PubMed/NCBI | |
Nishikawa T, Brownlee M and Araki E: Mitochondrial reactive oxygen species in the pathogenesis of early diabetic nephropathy. J Diabetes Investig. 6:137–139. 2015. View Article : Google Scholar : PubMed/NCBI | |
Kamiyama M, Urushihara M, Morikawa T, Konishi Y, Imanishi M, Nishiyama A and Kobori H: Oxidative stress/angiotensinogen/renin-angiotensin system axis in patients with diabetic nephropathy. Int J Mol Sci. 14:23045–23062. 2013. View Article : Google Scholar : PubMed/NCBI | |
Liu J, Wang C, Liu F, Lu Y and Cheng J: Metabonomics revealed xanthine oxidase-induced oxidative stress and inflammation in the pathogenesis of diabetic nephropathy. Anal Bioanal Chem. 407:2569–2579. 2015. View Article : Google Scholar : PubMed/NCBI | |
Tabur S, Korkmaz H, Eren MA, Oğuz E, Sabuncu T and Aksoy N: Urotensin-II level and its association with oxidative stress in early diabetic nephropathy. J Diabetes Complications. 29:115–119. 2015. View Article : Google Scholar : PubMed/NCBI | |
Mao ZM, Shen SM, Wan YG, Sun W, Chen HL, Huang MM, Yang JJ, Wu W, Tang HT and Tang RM: Huangkui capsule attenuates renal fibrosis in diabetic nephropathy rats through regulating oxidative stress and p38MAPK/Akt pathways, compared to α-lipoic acid. J Ethnopharmacol. 173:256–265. 2015. View Article : Google Scholar : PubMed/NCBI | |
Pal PB, Sinha K and Sil PC: Mangiferin attenuates diabetic nephropathy by inhibiting oxidative stress mediated signaling cascade, TNFα related and mitochondrial dependent apoptotic pathways in streptozotocin-induced diabetic rats. PLoS One. 9:e1072202014. View Article : Google Scholar : PubMed/NCBI | |
Kolati SR, Kasala ER, Bodduluru LN, Mahareddy JR, Uppulapu SK, Gogoi R, Barua CC and Lahkar M: BAY 11–7082 ameliorates diabetic nephropathy by attenuating hyperglycemia-mediated oxidative stress and renal inflammation via NF-κB pathway. Environ Toxicol Pharmacol. 39:690–699. 2015. View Article : Google Scholar : PubMed/NCBI | |
Yang B, Li XP, Ni YF, Du HY, Wang R, Li MJ, Wang WC, Li MM, Wang XH, Li L, et al: Protective effect of isorhamnetin on lipopolysaccharide-induced acute lung injury in mice. Inflammation. 39:129–137. 2016. View Article : Google Scholar : PubMed/NCBI | |
Chen TL, Zhu GL, Wang JA, Zhang GD, Liu HF, Chen JR, Wang Y and He XL: Protective effects of isorhamnetin on apoptosis and inflammation in TNF-α-induced HUVECs injury. Int J Clin Exp Pathol. 8:2311–2320. 2015.PubMed/NCBI | |
Dou W, Zhang J, Li H, Kortagere S, Sun K, Ding L, Ren G, Wang Z and Mani S: Plant flavonol isorhamnetin attenuates chemically induced inflammatory bowel disease via a PXR-dependent pathway. J Nutr Biochem. 25:923–933. 2014. View Article : Google Scholar : PubMed/NCBI | |
Manu KA, Shanmugam MK, Ramachandran L, Li F, Siveen KS, Chinnathambi A, Zayed ME, Alharbi SA, Arfuso F, Kumar AP, et al: Isorhamnetin augments the anti-tumor effect of capeciatbine through the negative regulation of NF-κB signaling cascade in gastric cancer. Cancer Lett. 363:28–36. 2015. View Article : Google Scholar : PubMed/NCBI | |
Qian C, Zhu C, Yu W, Jiang X and Zhang F: High-fat diet/low-dose streptozotocin- induced type 2 diabetes in rats impacts ostegenesis and Wnt signaling in bone marrow stromal cells. PLoS One. 10:e01363902015. View Article : Google Scholar : PubMed/NCBI | |
Zimmet P, Alberti KG and Shaw J: Global and societal implications of the diabetes epidemic. Nature. 414:782–787. 2001. View Article : Google Scholar : PubMed/NCBI | |
Ruggenenti P, Cravedi P and Remuzzi G: The RAAS in the pathogenesis and treatment of diabetic nephropathy. Nat Rev Nephrol. 6:319–330. 2010. View Article : Google Scholar : PubMed/NCBI | |
Brenner BM, Cooper ME, de Zeeuw D, Keane WF, Mitch WE, Parving HH, Remuzzi G, Snapinn SM, Zhang Z and Shahinfar S: RENAAL Study Investigators: Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy. N Engl J Med. 345:861–869. 2001. View Article : Google Scholar : PubMed/NCBI | |
Kim B, Choi YE and Kim HS: Eruca sativa and its flavonoid components, quercetin and isorhamnetin, improve skin barrier function by activation of peroxisome proliferator-activated receptor (PPAR)-α and suppression of inflammatory cytokines. Phytother Res. 28:1359–1366. 2014. View Article : Google Scholar : PubMed/NCBI | |
Yang JH, Shin BY, Han JY, Kim MG, Wi JE, Kim YW, Cho IJ, Kim SC, Shin SM and Ki SH: Isorhamnetin protects against oxidative stress by activating Nrf2 and inducing the expression of its target genes. Toxicol Appl Pharmacol. 274:293–301. 2014. View Article : Google Scholar : PubMed/NCBI | |
Dong GZ, Lee JH, Ki SH, Yang JH, Cho IJ, Kang SH, Zhao RJ, Kim SC and Kim YW: AMPK activation by isorhamnetin protects hepatocytes against oxidative stress and mitochondrial dysfunction. Eur J Pharmacol. 740:634–640. 2014. View Article : Google Scholar : PubMed/NCBI | |
Duran-Salgado MB and Rubio-Guerra AF: Diabetic nephropathy and inflammation. World J Diabetes. 5:393–398. 2014. View Article : Google Scholar : PubMed/NCBI | |
Lazaro I, Oguiza A, Recio C, Mallavia B, Madrigal-Matute J, Blanco J, Egido J, Martin-Ventura JL and Gomez-Guerrero C: Targeting HSP90 ameliorates nephropathy and atherosclerosis through suppression of NF-κB and STAT signaling pathways in diabetic mice. Diabetes. 64:3600–3613. 2015. View Article : Google Scholar : PubMed/NCBI | |
Sakai N and Wada T: Revisiting inflammation in diabetic nephropathy: The role of the Nlrp3 inflammasome in glomerular resident cells. Kidney Int. 87:12–14. 2015. View Article : Google Scholar : PubMed/NCBI | |
Jin JY, Choi EY, Park HR, Choi JI, Choi IS and Kim SJ: Isorhamnetin inhibits Prevotella intermedia lipopolysaccharide-induced production of interleukin-6 in murine macrophages via anti-inflammatory heme oxygenase-1 induction and inhibition of nuclear factor-κB and signal transducer and activator of transcription 1 activation. J Periodontal Res. 48:687–695. 2013.PubMed/NCBI | |
Muchová J, Országhová Z, Žitnanová I, Trebatický B, Breza J and Duracková Z: The effect of natural polyphenols on the oxidative stress markers in patients with diabetic nephropathy. Free Radic Biol Med. 75(Suppl 1): S422014. View Article : Google Scholar | |
Verma AK, Chandra S, Singh RG, Singh TB, Srivastava S and Srivastava R: Serum prolidase activity and oxidative stress in diabetic nephropathy and end stage renal disease: a correlative study with glucose and creatinine. Biochem Res Int. 2014:2914582014. View Article : Google Scholar : PubMed/NCBI | |
Gomes IB, Porto ML, Santos MC, Campagnaro BP, Pereira TM, Meyrelles SS and Vasquez EC: Renoprotective, anti-oxidative and anti-apoptotic effects of oral low-dose quercetin in the C57BL/6J model of diabetic nephropathy. Lipids Health Dis. 13:1842014. View Article : Google Scholar : PubMed/NCBI | |
Mima A: Inflammation and oxidative stress in diabetic nephropathy: new insights on its inhibition as new therapeutic targets. J Diabetes Res. 2013:2485632013. View Article : Google Scholar : PubMed/NCBI | |
Bao M and Lou Y: Isorhamnetin prevent endothelial cell injuries from oxidized LDL via activation of p38MAPK. Eur J Pharmacol. 547:22–30. 2006. View Article : Google Scholar : PubMed/NCBI | |
Han X, Piao MJ, Kim KC, Madduma Hewage SR, Yoo ES, Koh YS, Kang HK, Shin JH, Park Y, Yoo SJ, et al: Isorhamnetin Protects Human Keratinocytes against Ultraviolet B-Induced Cell Damage. Biomol Ther (Seoul). 23:357–366. 2015. View Article : Google Scholar : PubMed/NCBI | |
Ding Y, Yang H, Xiang W, He X, Liao W and Yi Z: CD200R1 agonist attenuates LPS-induced inflammatory response in human renal proximal tubular epithelial cells by regulating TLR4-MyD88-TAK1-mediated NF-κB and MAPK pathway. Biochem Biophys Res Commun. 460:287–294. 2015. View Article : Google Scholar : PubMed/NCBI |