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川芎嗪刺激啮齿动物远端结肠中囊性纤维化跨膜传导调节因子介导的阴离子分泌。

Tetramethylpyrazine stimulates cystic fibrosis transmembrane conductance regulator-mediated anion secretion in distal colon of rodents.

作者信息

He Qiong, Zhu Jin-Xia, Xing Ying, Tsang Lai-Ling, Yang Ning, Rowlands Dewi Kenneth, Chung Yiu-Wa, Chan Hsiao-Chang

机构信息

Department of Physiology, Zhengzhou University, Henan Province, China.

出版信息

World J Gastroenterol. 2005 Jul 21;11(27):4173-9. doi: 10.3748/wjg.v11.i27.4173.

Abstract

AIM

To investigate the effect of tetramethylpyrazine (TMP), an active compound from Ligustium Wollichii Franchat, on electrolyte transport across the distal colon of rodents and the mechanism involved.

METHODS

The short-circuit current (I(SC)) technique in conjunction with pharmacological agents and specific inhibitors were used in analyzing the electrolyte transport across the distal colon of rodents. The underlying cellular signaling mechanism was investigated by radioimmunoassay analysis (RIA) and a special mouse model of cystic fibrosis.

RESULTS

TMP stimulated a concentration-dependent rise in I(SC), which was dependent on both Cl(-) and HCO(3)(-), and inhibited by apical application of diphenylamine-2,2'-dicarboxylic acid (DPC) and glibenclamide, but resistant to 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid disodium salt hydrate (DIDS). Removal of Na(+) from basolateral solution almost completely abolished the I(SC) response to TMP, but it was insensitive to apical Na(+) replacement or apical Na(+) channel blocker, amiloride. Pretreatment of colonic mucosa with BAPTA-AM, a membrane-permeable selective Ca(2+) chelator, did not significantly alter the TMP-induced I(SC). No additive effect of forskolin and 3-isobutyl-1-methylxanthine (IBMX) was observed on the TMP-induced I(SC), but it was significantly reduced by a protein kinase A inhibitor, H(89). RIA results showed that TMP (1 mmol/L) elicited a significant increase in cellular cAMP production, which was similar to that elicited by the adenylate cyclase activator, forskolin (10 micromol/L). The TMP-elicited I(SC) as well as forskolin- or IBMX-induced I(SC) were abolished in mice with homozygous mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) presenting defective CFTR functions and secretions.

CONCLUSION

TMP may stimulate cAMP-dependent and CFTR-mediated Cl(-) and HCO(3)(-) secretion. This may have implications in the future development of alternative treatment for constipation.

摘要

目的

研究川芎活性成分川芎嗪(TMP)对啮齿动物远端结肠电解质转运的影响及其作用机制。

方法

采用短路电流(I(SC))技术结合药理学试剂和特异性抑制剂,分析TMP对啮齿动物远端结肠电解质转运的影响。通过放射免疫分析(RIA)和一种特殊的囊性纤维化小鼠模型研究其潜在的细胞信号转导机制。

结果

TMP刺激I(SC)呈浓度依赖性升高,这依赖于Cl(-)和HCO(3)(-),顶端应用二苯胺-2,2'-二羧酸(DPC)和格列本脲可抑制该作用,但对4,4'-二异硫氰基芪-2,2'-二磺酸二钠盐一水合物(DIDS)耐药。从基底外侧溶液中去除Na(+)几乎完全消除了TMP引起的I(SC)反应,但对顶端Na(+)置换或顶端Na(+)通道阻滞剂氨氯地平不敏感。用膜通透性选择性Ca(2+)螯合剂BAPTA-AM预处理结肠黏膜,并未显著改变TMP诱导的I(SC)。福斯高林和3-异丁基-1-甲基黄嘌呤(IBMX)对TMP诱导的I(SC)无相加作用,但蛋白激酶A抑制剂H(89)可使其显著降低。RIA结果显示,TMP(1 mmol/L)引起细胞内cAMP生成显著增加,这与腺苷酸环化酶激活剂福斯高林(10 μmol/L)引起的情况相似。在囊性纤维化跨膜传导调节因子(CFTR)纯合突变且CFTR功能和分泌存在缺陷的小鼠中,TMP诱导的I(SC)以及福斯高林或IBMX诱导的I(SC)均被消除。

结论

TMP可能刺激cAMP依赖的、CFTR介导的Cl(-)和HCO(3)(-)分泌。这可能对未来便秘替代治疗的发展具有重要意义。

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