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Niazirin from Moringa oleifera Lam. attenuates high glucose-induced oxidative stress through PKCζ/Nox4 pathway
Fang Wang1, Yifan Bao1, Xinchun Shen1
1College of Food Science and Engineering/Collaborative Innovation Center for Modern Grain Circulation and Safety/Key Laboratory of Grains and Oils Quality Control and Processing, Nanjing University of Finance and Economics, Nanjing 210023, China.
Background:
Diabetic complications-coronary atherosclerosis is closely related to the increased reactive oxygen species (ROS) induced by hyperglycemia. ROS are reported to induce the abnormal proliferation of vascular smooth muscle cells (VSMCs) under high glucose conditions. Leaf and seed extracts from Moringa oleifera are found to exhibit antioxidant activity. However, few studies are evaluating the antioxidant activities of chemical compounds isolated from the M. oleifera especially in cardiovascular field.
Purpose:
The aim of this study is to explore the antioxidative effect during hyperglycemia of niazirin from M. oleifera.
Study Design:
A cell model was applied.
Methods:
After the taking the in vitro antioxidant experiment including ferric reducing antioxidant power (FRAP), 2,2'-azinobis-(3-ethylbenzthiazoline-6-sulphonate) (ABTS) assay and 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. Cell viability was carried out using high glucose-induced VSMCs model. ROS production was tested by 2',7'-dichlorofluorescein diacetate (DCF-DA) assay. The protein kinase C zeta (PKCζ) and NADPH oxidase 4 (Nox 4) expression in vitro and in vivo were measured by western blot analysis.
Results:
Niazirin showed good free radical scavenging activity. Niazirin significantly attenuated the proliferation of high glucose-induced VSMCs. Furthermore, it could decrease the ROS and malondialdehyde (MDA) productions, while increased total antioxidant capacity (T-AOC), superoxide dismutase (SOD) as well as glutathione peroxidase (GPx) levels in high glucose-induced VSMCs and streptozotocin-induced mice. In addition, niazirin could eliminate the high glucose-induced PKCζ activation, indicated by Thr410 phosphorylation and inhibition of the Nox4 protein expression in vitro and in vivo.
Conclusion:
Niazirin from M. oleifera exhibited notably antioxidant activities and could be utilized as a potential natural antioxidant in preventing diabetic atherosclerosis.
Insights
Niazirin from Moringa oleifera demonstrates significant antioxidant activity, reducing reactive oxygen species (ROS) and vascular smooth muscle cell proliferation. This natural compound shows promise in preventing diabetic atherosclerosis.
Area of Science:
- Cardiovascular Pharmacology
- Natural Product Chemistry
- Oxidative Stress Research
Background:
- Diabetic atherosclerosis is linked to hyperglycemia-induced reactive oxygen species (ROS), which promote vascular smooth muscle cell (VSMC) proliferation.
- Moringa oleifera extracts possess antioxidant properties, but specific compounds' cardiovascular effects are understudied.
Purpose of the Study:
- To investigate the antioxidant effects of niazirin, a compound from Moringa oleifera, under hyperglycemic conditions.
Main Methods:
- In vitro antioxidant assays (FRAP, ABTS, DPPH) and cell viability tests on high glucose-induced VSMCs.
- Measurement of ROS production, malondialdehyde (MDA), total antioxidant capacity (T-AOC), superoxide dismutase (SOD), and glutathione peroxidase (GPx).
- Western blot analysis of protein kinase C zeta (PKCζ) and NADPH oxidase 4 (Nox 4) expression in vitro and in vivo.
Main Results:
- Niazirin exhibited potent free radical scavenging activity and attenuated VSMC proliferation under high glucose.
- It reduced ROS and MDA levels while increasing T-AOC, SOD, and GPx in hyperglycemic VSMCs and mice.
- Niazirin inhibited high glucose-induced PKCζ activation and Nox4 protein expression.
Conclusions:
- Niazirin from Moringa oleifera possesses significant antioxidant properties.
- It effectively mitigates oxidative stress and cellular damage associated with hyperglycemia.
- Niazirin is a potential natural antioxidant for preventing diabetic atherosclerosis.
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