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首页> 外文期刊>Acta physiologica Scandinavica >Serosal application of Ba(2+) induces oscillatory chloride secretion via activation of submucosal cholinergic neurones in guinea-pig distal colon.
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Serosal application of Ba(2+) induces oscillatory chloride secretion via activation of submucosal cholinergic neurones in guinea-pig distal colon.

机译:浆液中Ba(2+)的应用通过豚鼠远端结肠粘膜下胆碱能神经元的激活诱导氯化物的分泌。

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摘要

The enteric nervous system regulates ion and fluid secretion in the mammalian intestine at both resting and stimulated conditions. To determine the type and activation mechanism of neurones involved, mucosa-submucosa sheets isolated from guinea-pig distal colon were studied in vitro in Ussing chambers. Serosal addition of 0.5-1 mM barium (Ba(2+)), a potassium (K(+)) channel inhibitor, caused oscillatory increases in short-circuit current (I(sc)). Mean values of the size and frequency of I(sc) were 369.1 microA cm(-2) and 2.3 min(-1). The oscillatory I(sc) induced by the low concentrations of Ba(2+) was blocked by either higher concentrations of Ba(2+) (2-5 mM) or other K(+) channel inhibitors, such as tetraethylammonium (TEA) (1 mM) and quinine (20 mM). The Ba(2+)-induced oscillatory I(sc) was also inhibited by tetrodotoxin (TTX) and atropine. In a nominally Ca(2+) free solution plus serosal addition of 0.1 mM ethylene glycol-bis (beta-aminoethyl ether) N,N,N',N'-tetraacetic acid (EGTA), a Ca(2+) chelator, the oscillatory I(sc) slowed and diminished. Further, the Ba(2+)-induced oscillatory I(sc) was partially inhibited by apical addition of 100 microM 5'-nitro-2-(3-phenylpropylamino)benzoic-acid (NPPB), a Cl(-) channel inhibitor, and completely disappeared in a low Cl(-) solution (11 mM) on both sides. On the other hand, application of either cimetidine, a histamine H(2) receptor antagonist, or hexamethonium, a nicotinic antagonist, to the serosal side did not affect the Ba(2+)-induced oscillatory I(sc). In conclusion, the Ba(2+)-induced oscillatory I(sc) is the transepithelial Cl(-) current which is stimulated by activation of cholinergic neurones in submucosal plexus of guinea-pig distal colon.
机译:肠道神经系统在静止和刺激条件下均能调节哺乳动物肠道中的离子和液体分泌。为了确定所涉及的神经元的类型和激活机制,在Ussing室中对从豚鼠远端结肠分离的粘膜下粘膜下层进行了体外研究。浆膜添加0.5-1 mM钡(Ba(2+)),钾(K(+))通道抑制剂,引起短路电流(I(sc))振荡增加。 I(sc)的大小和频率平均值为369.1 microA cm(-2)和2.3 min(-1)。低浓度的Ba(2+)诱导的振荡I(sc)被较高浓度的Ba(2+)(2-5 mM)或其他K(+)通道抑制剂(例如四乙铵(TEA))阻止(1 mM)和奎宁(20 mM)。 Ba(2+)诱导的振荡I(sc)也被河豚毒素(TTX)和阿托品抑制。在名义上不含Ca(2+)的溶液中,加上浆膜添加0.1 mM乙二醇-双(β-氨基乙基醚)N,N,N',N'-四乙酸(EGTA),Ca(2+)螯合剂,振荡I(sc)减慢并减小。此外,通过添加100 microM 5'-硝基-2-(3-苯基丙基氨基)苯甲酸(NPPB),Cl(-)通道抑制剂来部分抑制Ba(2+)诱导的振荡I(sc)。 ,并在两侧的低Cl(-)溶液(11 mM)中完全消失。另一方面,将西咪替丁,组胺H(2)受体拮抗剂或六甲铵(烟碱类拮抗剂)应用于浆膜侧,不会影响Ba(2+)诱导的振荡I(sc)。总之,Ba(2+)诱导的振荡I(sc)是跨上皮Cl(-)电流,该电流受豚鼠远端结肠粘膜下丛中胆碱能神经元的激活刺激。

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