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糖苷刺激亚种(M.A. Rau)K.K. Khanna & An. Kumar 的葡萄糖摄取:TNF-α 诱导 L6 成肌细胞胰岛素抵抗的研究。

Stimulation of glucose uptake by glycosides from subsp. (M.A. Rau) K.K. Khanna & An. Kumar: An study of TNF-α induced insulin resistance in L6 myoblasts.

机构信息

Analytical Chemistry Department, Phytochemistry Division, CSIR-Central Institute of Medicinal and Aromatic Plants, Lucknow, India.

Bioprospection Department, CSIR-Central Institute of Medicinal and Aromatic Plants, Lucknow, India.

出版信息

Nat Prod Res. 2023 Jun;37(12):2024-2030. doi: 10.1080/14786419.2022.2112957. Epub 2022 Aug 19.

DOI:10.1080/14786419.2022.2112957
PMID:35983769
Abstract

subsp. (M.A. Rau) K.K. Khanna & An. Kumar (Orobanchaceae) is a parasitic plant indigenous to India. Locally, the plant is known as ' and . It is used to treat fever, piles, cardiovascular disorders, and blood-borne non-infectious diseases by ethnic communities. The phytochemical investigation of subsp. rhizome led to the isolation of azafrin (), rehmaionoside-C (), and mussaenoside (). Compounds ( and () are being reported for the first time from this plant. Compounds were evaluated for their intercellular glucose uptake activity in basal and insulin-TNF-α-stimulated L6 muscle cells. In particular, rehmaionoside C exhibited activity comparative to metformin, increasing uptake by basal- and insulin-TNF-αstimulated cells by 4.88- and 3.90-fold and 5.04- and 4.04-fold. While azafrin and mussaenoside have produced 3.03- and 2.36-fold; 4.03- and 3.22-fold increase in intercellular glucose uptake. Compounds did not show toxicities in rat L6 myoblast cells. The study suggests that rehmaionoside-C from subsp. might activate glucose uptake by insulin mimics and could be a nontoxic anti-diabetes lead for drug discovery.

摘要

(M.A. Rau)K.K. Khanna & An. Kumar(列当科)是一种原产于印度的寄生植物。在当地,这种植物被称为“和”。它被民族社区用于治疗发热、痔疮、心血管疾病和血液传播的非传染性疾病。对 亚种根茎的植物化学研究导致分离出了氮杂佛林()、瑞马酮 C()和麦萨诺苷()。化合物(和()是首次从该植物中报道的。对化合物进行了评价,以研究它们在基础状态和胰岛素-TNF-α刺激的 L6 肌肉细胞中的细胞间葡萄糖摄取活性。特别是,瑞马酮 C 表现出与二甲双胍相当的活性,使基础状态和胰岛素-TNF-α刺激的细胞的摄取分别增加了 4.88-和 3.90 倍和 5.04-和 4.04 倍。而氮杂佛林和麦萨诺苷分别产生了 3.03-和 2.36 倍;4.03-和 3.22 倍的细胞间葡萄糖摄取增加。化合物在大鼠 L6 成肌细胞中没有显示出毒性。该研究表明, 亚种中的瑞马酮 C 可能通过胰岛素模拟物激活葡萄糖摄取,并且可能是一种无毒的抗糖尿病药物发现先导化合物。

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