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桑桂饮通过抑制 db/db 小鼠和 MIN6 胰岛β细胞内质网应激和自噬预防棕榈酸诱导的细胞凋亡。

Sangguayin preparation prevents palmitate-induced apoptosis by suppressing endoplasmic reticulum stress and autophagy in db/db mice and MIN6 pancreatic β-cells.

机构信息

Department of pharmacy, Xiangtan Central Hospital, Xiangtan 411100, China.

Department of pharmacy, Xiangtan Central Hospital, Xiangtan 411100, China.

出版信息

Chin J Nat Med. 2020 Jun;18(6):472-480. doi: 10.1016/S1875-5364(20)30054-6.

Abstract

Sangguayin preparation (SGY-P) is refined from the traditional Chinese medicinal compound Sangguayin, which "clears heat and promotes fluid" and "tonifies kidney and spleen" for "Xiaoke", commonly known as 'Diabetes mellitus' in clinics. Previous studies have shown that SGY-P could reduce insulin resistance and repair damaged pancreas in db/db mice, but the underlying mechanisms were unclear. Here, we investigated whether treatment with SGY-P could protect pancreatic β-cells from apoptosis and uncovered the underlying mechanisms. db/db mice were used to observe the hypoglycemic and islet protective effect in vivo. Apoptosis was induced in mouse insulinoma 6 (MIN6) cells by palmitate, following which the cells were treated with SGY-P for elucidating the anti-apoptotic mechanism in vitro. Cell viability and nuclear morphology were detected by CCK-8 assay and Hoechst 33258 staining. The expression levels of apoptosis-, endoplasmic reticulum (ER) stress-, and autophagy-related proteins were measured by western blot. The results showed that SGY-P reduced fasting blood glucose, pancreatic pathological changes, and islet β-cell apoptosis in db/db mice. Palmitate-induced apoptosis in MIN6 cells was decreased by SGY-P treatment. Hence, SGY-P therapy exhibited a protective effect on pancreatic β-cells by decreasing the expression of cleaved caspase-3, cleaved PARP and Bax, and increasing Bcl-2 by suppressing ER stress (Bip/XBP1/IRE1α/CHOP/Caspase-12) and autophagy (LC3/p62/Atg5) pathways.2/Atg5) pathways.

摘要

降糖益肾方(SGY-P)是由传统中药方剂降糖益肾方精制而成,具有“清热生津”、“补肾健脾”的功效,常用于临床“消渴”,即“糖尿病”。既往研究表明,SGY-P 可降低 db/db 小鼠的胰岛素抵抗,修复受损的胰腺,但具体机制尚不清楚。本研究旨在探讨 SGY-P 是否能保护胰岛β细胞免受凋亡,并揭示其潜在机制。采用 db/db 小鼠观察体内降糖和胰岛保护作用,用棕榈酸诱导小鼠胰岛素瘤 6(MIN6)细胞凋亡,然后用 SGY-P 处理细胞,阐明其体外抗凋亡机制。通过 CCK-8 法和 Hoechst 染色检测细胞活力和核形态。Western blot 检测凋亡、内质网(ER)应激和自噬相关蛋白的表达水平。结果表明,SGY-P 降低了 db/db 小鼠的空腹血糖、胰腺病理变化和胰岛β细胞凋亡。SGY-P 处理可减少棕榈酸诱导的 MIN6 细胞凋亡。因此,SGY-P 治疗通过抑制 ER 应激(Bip/XBP1/IRE1α/CHOP/Caspase-12)和自噬(LC3/p62/Atg5)途径,降低 cleaved caspase-3、cleaved PARP 和 Bax 的表达,增加 Bcl-2 的表达,对胰岛β细胞发挥保护作用。

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