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澳大利亚帚尾袋貂(Trichosurus vulpecula)肠道中的电生性离子转运:有袋类动物新型转运模式的迹象

Electrogenic ion transport in the intestine of the Australian common brushtail possum, Trichosurus vulpecula: indications of novel transport patterns in a marsupial.

作者信息

Butt A G, Mathieson S E, McLeod B J

机构信息

Department of Physiology, School of Medical Sciences, University of Otago, PO Box 913 Dunedin, New Zealand.

出版信息

J Comp Physiol B. 2002 Aug;172(6):495-502. doi: 10.1007/s00360-002-0275-y. Epub 2002 Jun 26.

Abstract

In this study, electrogenic ion transport in the intestine of the Australian common brushtail possum, Trichosurus vulpecula was investigated. In the ileum, a Na(+)-dependent, phloridzin- and amiloride-insensitive short-circuit current ( Isc) was present. Mucosal glucose stimulated a further phloridzin-sensitive, dose-dependent increase in Isc. A Na(+)-dependent, ouabain-sensitive Isc was also present in the caecum and colon. In the proximal and distal colon, amiloride (100 micro mol l(-1), mucosal) inhibited this Isc by 81+/-4% and 65+/-3%, respectively and the Ki for amiloride (approximately 1 micro mol l(-1)) was consistent with the inhibition of a classical epithelial Na(+) channel. In the caecum, 50% of the Isc was inhibited by amiloride (100 micro mol l(-1), mucosal). The amiloride-insensitive Isc in the colon was not due to electrogenic Cl(-) secretion, as serosal bumetanide (100 micro mol l(-1)) had no effect on the Isc. Furthermore, the secretagogues forskolin (10 micro mol l(-1)), carbachol (100 micro mol l(-1)) and dibutyryl-cAMP or dibutyryl-cGMP (100 micro mol l(-1)) did not stimulate electrogenic Cl(-) secretion by the colon. These results indicate that the transport properties of the hindgut of the possum differ significantly from those of eutherian mammals and may be associated with different functions of the hindgut of possums when compared to eutherian mammals.

摘要

在本研究中,对澳大利亚普通帚尾袋貂(Trichosurus vulpecula)肠道中的生电离子转运进行了研究。在回肠中,存在一种依赖Na⁺、对根皮苷和氨氯吡咪不敏感的短路电流(Isc)。黏膜葡萄糖刺激Isc进一步出现根皮苷敏感的、剂量依赖性增加。在盲肠和结肠中也存在依赖Na⁺、对哇巴因敏感的Isc。在近端结肠和远端结肠中,氨氯吡咪(100 μmol l⁻¹,黏膜给药)分别使该Isc抑制81±4%和65±3%,氨氯吡咪的Ki(约1 μmol l⁻¹)与经典上皮Na⁺通道的抑制情况一致。在盲肠中,氨氯吡咪(100 μmol l⁻¹,黏膜给药)使50%的Isc受到抑制。结肠中对氨氯吡咪不敏感的Isc并非由生电Cl⁻分泌所致,因为浆膜给予布美他尼(100 μmol l⁻¹)对Isc无影响。此外,促分泌剂福斯可林(10 μmol l⁻¹)、卡巴胆碱(100 μmol l⁻¹)以及二丁酰-cAMP或二丁酰-cGMP(100 μmol l⁻¹)均未刺激结肠的生电Cl⁻分泌。这些结果表明,袋貂后肠的转运特性与真兽类哺乳动物有显著差异,并且与袋貂后肠相对于真兽类哺乳动物的不同功能可能相关。

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