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氨基酸抑制月桂酸钠(一种吸收促进剂)诱导的细胞凋亡。

Amino acids suppress apoptosis induced by sodium laurate, an absorption enhancer.

机构信息

Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Okayama University, 1-1-1 Tsushima-naka, Okayama 700-8530, Japan.

出版信息

J Pharm Sci. 2009 Dec;98(12):4629-38. doi: 10.1002/jps.21757.

Abstract

The formulation containing sodium laurate (C12), an absorption enhancer, and several amino acids such as taurine (Tau) and L-glutamine (L-Gln) is a promising preparation that can safely improve the intestinal absorption of poorly absorbable drugs. The safety for intestinal mucosa is achieved because the amino acids prevent C12 from causing mucosal damages via several mechanisms. In the present study, the possible involvement of apoptosis, programmed cell death, in mucosal damages caused by C12 and cytoprotection by amino acids was examined. C12 induced DNA fragmentation, a typical phenomenon of apoptosis, in rat large-intestinal epithelial cells while the addition of amino acids significantly attenuated it. C12 alone significantly increased the release of cytochrome C, an apoptosis-inducing factor, from mitochondria, which could be via the decrease in the level of Bcl-2, an inhibiting factor of cytochrome C release. The enhancement of cytochrome C release by C12 led to the activation of caspase 9, an initiator enzyme, and the subsequent activation of caspase 3, an effector enzyme. On the other hand, Tau or L-Gln significantly suppressed the release of cytochrome C from mitochondria and attenuated the activities of both caspases, which could be attributed to the maintenance of Bcl-2 expression.

摘要

含有月桂酸钠(C12)、吸收增强剂和牛磺酸(Tau)和 L-谷氨酰胺(L-Gln)等几种氨基酸的配方是一种很有前途的制剂,它可以安全地提高难吸收药物的肠道吸收。由于氨基酸通过几种机制防止 C12 引起粘膜损伤,因此对肠粘膜是安全的。在本研究中,检查了 C12 引起的粘膜损伤和氨基酸的细胞保护作用中细胞凋亡(程序性细胞死亡)的可能参与。C12 在大鼠大肠上皮细胞中诱导 DNA 片段化,这是细胞凋亡的典型现象,而添加氨基酸则显著减弱了这种现象。C12 本身可显著增加细胞色素 C(一种凋亡诱导因子)从线粒体中的释放,这可能是通过降低细胞色素 C 释放的抑制因子 Bcl-2 的水平来实现的。C12 增强细胞色素 C 释放导致起始酶 caspase 9 的激活,以及随后的效应酶 caspase 3 的激活。另一方面,Tau 或 L-Gln 可显著抑制线粒体中细胞色素 C 的释放,并减弱两种半胱天冬酶的活性,这可能归因于 Bcl-2 表达的维持。

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