Citation:
HU Yong-Sheng, XU Peng-Tao, YE Sheng-Jie, SHI Wen-Yu, GAO Hong-Chang, ZHUO Yang, ZHAO Liang-Cai. Effects of Celastrol on Accelerated Healing of Skin Wounds of Diabetic Ulceration in Rats and Mechanism Revealed by Nuclear Magnetic Resonance-based Metabonomics[J]. Chinese Journal of Analytical Chemistry,
;2018, 46(2): 170-177.
doi:
10.11895/j.issn.0253-3820.170323
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The experimental SD rats were randomly divided into normal control group (Con group), diabetic ulcer model group (DM group) and Celastrol group (Cel group). Except the control group, diabetic ulceration rat models were established by intraperitoneal injection of streptozotocin along with skin scald. And then, each group was treated by spraying the saline solution on the affected skin with (Cel group) or without (Con group and DM group) Cel (q.d.×14 d). Nuclear magnetic resonance (NMR)-based metabonomic analysis was applied to detect metabolic characteristics, accompanied by healing rate calculation and HE and Masson staining to study therapeutic effect of celastrol on accelerated healing of skin wounds of diabetic ulceration rats, which could be used to elucidate therapeutic effects of celastrol on the rat diabetic ulceration and its mechanism. The results showed that celastrol could induce epithelial regeneration of the rat ulcer wound, regulate the infiltration of inflammatory cells and the distribution of collagen fibers, and promote the healing of the ulcer wound. About 20 endogenous potential differential metabolites were screened and identified by partial least square analysis. Metabolic pathway analysis was carried out to show that celastrol can significantly recovery the level of the tricarboxylic acid cycle, promote its energy supply, accelerate the protein synthesis, improve mitochondrial dysfunction and oxidative stress, and accelerate the self-repair ability of skin tissue. Celastrol can promote the healing of ulcers skins of the diabetic rats, which contribute to experimental basis of the drugs for the treatment of diabetic ulcers.
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