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福斯高林可诱导氯离子通过大鼠降结肠的离体黏膜进行分泌。

Forskolin induced chloride secretion across the isolated mucosa of rat colon descendens.

作者信息

Bridges R J, Rummel W, Simon B

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1983 Aug;323(4):355-60. doi: 10.1007/BF00512476.

Abstract

The effects of forskolin, a diterpene reported to stimulate adenylate cyclase, on electrolyte transport across the isolated colonic mucosa of rat colon descendens were investigated. Forskolin, over a concentration range of 10(-7)-10(-5) M, dose-dependently increased short circuit current (Isc) and transmural potential difference (Vms). The nearly 2-fold increase in Isc and Vms caused by forskolin was accompanied by a small increase in transmural conductance (Gt). The effects of forskolin were rapid and completely reversible without any loss in tissue sensitivity. Forskolin (5 X 10(-6) M) inhibited the absorption of Na+ and reversed Cl- absorption to secretion. These effects were due to an inhibition of the mucosal-to-serosal fluxes of Na+ and Cl-. Ion substitution experiments revealed that the effects of forskolin were both Na+ and Cl- dependent and these ions were required in the serosal solution. Furosemide (10(-4) M) as well as scilliroside (10(-4) M) reversed and prevented the increase in Isc caused by forskolin. Adenylate cyclase activity in homogenates of colonic mucosa was increased 3-fold by forskolin. These results with rat colon are compared with those reported for rabbit colon and ileum and the mechanism of cyclic-AMP induced Cl- secretion in these epithelia is discussed.

摘要

据报道,二萜类化合物福斯高林可刺激腺苷酸环化酶,本研究探讨了其对大鼠降结肠离体结肠黏膜电解质转运的影响。福斯高林在10(-7)-10(-5)M的浓度范围内,剂量依赖性地增加短路电流(Isc)和跨膜电位差(Vms)。福斯高林引起的Isc和Vms近2倍的增加伴随着跨膜电导(Gt)的小幅增加。福斯高林的作用迅速且完全可逆,组织敏感性无任何损失。福斯高林(5×10(-6)M)抑制Na+的吸收,并使Cl-的吸收逆转至分泌。这些作用是由于抑制了Na+和Cl-从黏膜到浆膜的通量。离子置换实验表明,福斯高林的作用既依赖于Na+也依赖于Cl-,且这些离子存在于浆膜溶液中是必需的。呋塞米(10(-4)M)以及海葱苷(10(-4)M)可逆转并阻止福斯高林引起的Isc增加。福斯高林使结肠黏膜匀浆中的腺苷酸环化酶活性增加了3倍。将大鼠结肠的这些结果与兔结肠和回肠的报道结果进行了比较,并讨论了这些上皮细胞中环磷酸腺苷诱导的Cl-分泌机制。

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