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枸杞多糖通过抑制 PI3K/Akt 通路介导的雄性小鼠异常自噬来减轻糖尿病睾丸功能障碍。

Lycium barbarum polysaccharide attenuates diabetic testicular dysfunction via inhibition of the PI3K/Akt pathway-mediated abnormal autophagy in male mice.

机构信息

College of Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.

Department of Pharmacology, Ningxia Medical University, Yinchuan, 750004, China.

出版信息

Cell Tissue Res. 2018 Dec;374(3):653-666. doi: 10.1007/s00441-018-2891-1. Epub 2018 Aug 2.

Abstract

Testicular dysfunction is one of the serious secondary complications in diabetes. Lycium barbarum polysaccharide (LBP) has long been considered to possess a wide range of beneficial properties including antiaging, anticancer and reproductive-enhancing. Abnormal autophagy was reported to play a significant role in accelerating diabetic reproductive injury. However, the autophagy regulation mechanism of LBP on diabetic testicular dysfunction is incompletely understood. We investigate the protective effects of LBP on diabetic testicular dysfunction and its underlying mechanism with different approaches. Protective effects of LBP (40 mg/kg) on testicular functions were assessed through the use of sperm parameters, testosterone levels and hematoxylin and eosin staining. Antioxidant capacity and serum malondialdehyde levels were determined using assay kits. Immune intensity of Beclin-1 and LC3I in testes was detected by immunofluorescence staining. Western blot analysis was used to detect expressions of p-PI3K, Akt, p-Akt, Beclin-1, LC3I and LC3II proteins. Q-PCR was used to evaluate Beclin-1 and LC3I mRNA expressions in testis. Administration of LBP (40 mg/kg) considerably recovered testicular function, obviously improved testicular histopathologic structure and significantly increased antioxidant enzyme activities. Immunofluorescence staining showed that immune intensity of Beclin-1 and LC3I significantly decreased in the LBP 40 mg/kg group. The results of Q-PCR and western blot analysis showed that LBP 40 mg/kg significantly downregulated Beclin-1 and LC3I protein expressions upregulated p-PI3K and p-Akt protein expressions and decreased Beclin-1 and LC3I mRNA expressions compared with diabetic mice. In conclusion, inhibition of PI3K/Akt pathway-mediated testicular excessive autophagy may be a target for protective effects of LBP on diabetic testicular dysfunction.

摘要

睾丸功能障碍是糖尿病的严重继发性并发症之一。枸杞多糖(LBP)长期以来被认为具有广泛的有益特性,包括抗衰老、抗癌和增强生殖能力。异常自噬被报道在加速糖尿病生殖损伤中起重要作用。然而,LBP 对糖尿病睾丸功能障碍的自噬调节机制尚不完全清楚。我们通过不同的方法研究了 LBP 对糖尿病睾丸功能障碍的保护作用及其潜在机制。通过使用精子参数、睾酮水平和苏木精和伊红染色来评估 LBP(40mg/kg)对睾丸功能的保护作用。使用试剂盒测定抗氧化能力和血清丙二醛水平。通过免疫荧光染色检测睾丸中 Beclin-1 和 LC3I 的免疫强度。通过 Western blot 分析检测 p-PI3K、Akt、p-Akt、Beclin-1、LC3I 和 LC3II 蛋白的表达。使用 Q-PCR 评估睾丸中 Beclin-1 和 LC3I mRNA 的表达。给予 LBP(40mg/kg)可显著恢复睾丸功能,明显改善睾丸组织病理学结构,显著提高抗氧化酶活性。免疫荧光染色显示,LBP 40mg/kg 组 Beclin-1 和 LC3I 的免疫强度显著降低。Q-PCR 和 Western blot 分析结果表明,与糖尿病小鼠相比,LBP 40mg/kg 可显著下调 Beclin-1 和 LC3I 蛋白表达,上调 p-PI3K 和 p-Akt 蛋白表达,降低 Beclin-1 和 LC3I mRNA 表达。总之,抑制 PI3K/Akt 通路介导的睾丸过度自噬可能是 LBP 对糖尿病睾丸功能障碍保护作用的靶点。

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