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Crocin improves renal function by declining Nox-4, IL-18, and p53 expression levels in an experimental model of
Habib Yaribeygi1,2, Mohammad T Mohammadi3,4, Ramin Rezaee5
1Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Abstract:
Oxidative damage, inflammation and apoptosis play significant roles in diabetic nephropathy. Previous studies demonstrated anti-inflammatory and anti-oxidative effects of crocin, but there is no evidence about its effects on IL-18, NOX-4, and p53 expression in diabetic kidneys. The aim of this study was to evaluate possible effects of crocin on improving main mechanisms underlying diabetic nephropathy. Male Wistar rats were randomly divided into four separate groups as normal (C), normal treated (CC), diabetic (D), and diabetic treated (DC) (n = 6). Diabetes was induced by a single dose of streptozotocin (40 mg/kg/intravenous). Treated groups received crocin (40 mg/kg, intraperitoneal) for 8 weeks. At the end of the 8th week of the study, all rats were sacrificed and urine, blood and tissue were collected. Levels of urea, uric acid, creatinine and glucose were determined collected sera, and proteinuria was measured in urine samples. Moreover, the contents of malondialdehyde (MDA), nitrate, and glutathione (GLT) as well as catalase (CAT) and superoxide dismutase (SOD) enzymes activities were measured. The expression of NOX-4, IL-18, and p53 at both mRNA and protein levels were also assessed. Hyperglycemia significantly increased proteinuria in diabetic rats (D). Also, depressed antioxidant defense system potency, but increased NOX-4 expression and free radicals production resulting in oxidative stress, were observed. Moreover, expressions of IL-18 (as a marker of inflammation) and p53 (as a marker of apoptosis) were increased. These outcomes were accompanied by enhanced histological damages and renal failure but, treatment with crocin improved these deteriorations, and ameliorated renal function. It potentiated renal cells antioxidant defense system and declined inflammation. Also, crocin lowered apoptosis and improved histological damages in renal cells. Oxidative stress, inflammation and apoptosis are considered three main mechanisms underlying diabetic nephropathy. Treatment with crocin prevented these deleterious effects and improved renal function under diabetic conditions.
Insights
Crocin treatment improved kidney function in diabetic rats by reducing oxidative stress, inflammation, and apoptosis. This study shows crocin
Area of Science:
- Nephrology
- Pharmacology
- Biochemistry
Background:
- Diabetic nephropathy is characterized by oxidative damage, inflammation, and apoptosis.
- Crocin exhibits anti-inflammatory and antioxidant properties, but its effects on key diabetic nephropathy markers are unknown.
Purpose of the Study:
- To investigate the effects of crocin on oxidative stress, inflammation, and apoptosis in a rat model of diabetic nephropathy.
- To assess crocin's impact on Interleukin-18 (IL-18), NADPH oxidase 4 (NOX-4), and p53 expression in diabetic kidneys.
Main Methods:
- Male Wistar rats were induced with diabetes using streptozotocin.
- Diabetic and normal rats were treated with crocin (40 mg/kg) or vehicle for 8 weeks.
- Kidney function, oxidative stress markers (MDA, GLT, CAT, SOD), and expression of NOX-4, IL-18, and p53 were evaluated.
Main Results:
- Diabetes significantly increased proteinuria, oxidative stress (elevated NOX-4, MDA; reduced GLT, CAT, SOD), inflammation (IL-18), and apoptosis (p53).
- Crocin treatment ameliorated renal function, reduced proteinuria, and improved antioxidant defense.
- Crocin significantly decreased NOX-4, IL-18, and p53 expression in diabetic kidneys.
Conclusions:
- Crocin effectively mitigates oxidative stress, inflammation, and apoptosis in diabetic nephropathy.
- Crocin treatment improves renal function and histological damage in diabetic conditions.
- Crocin demonstrates therapeutic potential for managing diabetic nephropathy.
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