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矢车菊素-3-O-(对香豆酰基鼠李糖苷)-5-O-葡萄糖苷对 D-半乳糖诱导衰老小鼠的多种保护作用。

Multi-Protective Effects of Petunidin-3-O-(-coumaroylrutinoside)-5-O-glucoside on D-Gal-Induced Aging Mice.

机构信息

Qinghai Provincial Key Laboratory of Tibetan Medicine Research and CAS Key Laboratory of Tibetan Medicine Research, Northwest Institute of Plateau Biology, Xining 810008, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Int J Mol Sci. 2024 Oct 13;25(20):11014. doi: 10.3390/ijms252011014.

Abstract

Petunidin-3-O-(-coumaroylrutinoside)-5-O-glucoside (PtCG), the primary anthocyanin ingredient in Murr., possesses a range of biological activities, including antioxidative properties and melanin inhibition. This study aimed to investigate the protective effect of PtCG on D-galactose (D-gal)-induced aging in female mice and elucidate the underlying molecular pathways. Behavioral experiments, including the MWW and Y-maze tests, revealed that PtCG significantly ameliorated cognitive decline and enhanced learning and memory abilities in aging mice. Regarding biochemical indicators, PtCG considerably improved superoxide dismutase (SOD) and glutathione (GSH) activity while reducing malondialdehyde (MDA) and acetylcholinesterase (AChE) levels in the hippocampus and serum. Furthermore, PtCG ingestion alleviated liver injury by decreasing alanine transaminase (ALT), aspartate transaminase (AST), and alkaline phosphatase (AKP) levels, and attenuated renal damage by reducing blood urea nitrogen (BUN) and uric acid (UA) levels. Transmission electron microscopy (TEM) results demonstrated that PtCG restored the function and quantity of synapses in the hippocampus. Hematoxylin and eosin (H&E), Masson's trichrome, and Nissl staining revealed that PtCG significantly improved the relevant pathological characteristics of liver and hippocampal tissues in aging mice. The molecular mechanism investigation showed that PtCG downregulated the protein expression of microglial marker ionized calcium-binding adapter molecule 1 (Iba1), astrocytic marker glial fibrillary acidic protein (GFAP), β-secretase 1 (BACE-1), and amyloid-beta (Aβ) in the hippocampus of aging mice. The protein expression of inflammatory pathway components, including nuclear factor-kappa B (NF-κB), cyclooxygenase-2 (COX2), inducible nitric oxide synthase (iNOS), and interleukin-1 beta (IL-1β), was also suppressed. These findings suggest that PtCG may possess anti-aging properties, with its mechanism of action potentially linked to the attenuation of neuroinflammation, oxidative stress, and liver and kidney damage. PtCG may have future applications as a functional food for the treatment of aging-related disorders.

摘要

矢车菊素-3-O-(-咖啡酰基芦丁苷)-5-O-葡萄糖苷(PtCG)是杨梅属植物中的主要花色苷成分,具有多种生物活性,包括抗氧化和抑制黑色素形成。本研究旨在探讨 PtCG 对 D-半乳糖(D-gal)诱导的雌性小鼠衰老的保护作用,并阐明其潜在的分子途径。行为实验,包括 MWW 和 Y 迷宫测试,表明 PtCG 可显著改善衰老小鼠的认知能力下降,并增强其学习和记忆能力。在生化指标方面,PtCG 可显著提高超氧化物歧化酶(SOD)和谷胱甘肽(GSH)的活性,同时降低海马体和血清中丙二醛(MDA)和乙酰胆碱酯酶(AChE)的水平。此外,PtCG 通过降低丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)和碱性磷酸酶(AKP)水平减轻肝损伤,并通过降低血尿素氮(BUN)和尿酸(UA)水平减轻肾损伤。透射电子显微镜(TEM)结果表明,PtCG 恢复了海马体中突触的功能和数量。苏木精和伊红(H&E)、马松三色和尼氏染色显示,PtCG 显著改善了衰老小鼠肝和海马组织的相关病理特征。分子机制研究表明,PtCG 下调了衰老小鼠海马体中小胶质细胞标志物离子钙结合接头分子 1(Iba1)、星形胶质细胞标志物胶质纤维酸性蛋白(GFAP)、β-分泌酶 1(BACE-1)和淀粉样β(Aβ)的蛋白表达。炎症通路成分,包括核因子-κB(NF-κB)、环氧化酶-2(COX2)、诱导型一氧化氮合酶(iNOS)和白细胞介素-1β(IL-1β)的蛋白表达也受到抑制。这些发现表明,PtCG 可能具有抗衰老特性,其作用机制可能与减轻神经炎症、氧化应激以及肝和肾损伤有关。PtCG 可能作为一种功能性食品,用于治疗与衰老相关的疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/097a/11506951/d339104782b4/ijms-25-11014-g001.jpg

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