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芳氨基苯甲酸酯类氯离子通道阻滞剂对兔结肠等效短路电流的影响。

Effects of arylaminobenzoate-type chloride channel blockers on equivalent short-circuit current in rabbit colon.

作者信息

Greger R, Nitschke R B, Lohrmann E, Burhoff I, Hropot M, Englert H C, Lang H J

机构信息

Physiologisches Institut, Albert-Ludwigs-Universität, Freiburg, Federal Republic of Germany.

出版信息

Pflugers Arch. 1991 Sep;419(2):190-6. doi: 10.1007/BF00373006.

Abstract

Arylaminobenzoates were examined in rabbit colon mounted in an Ussing chamber. The open-circuit transepithelial voltage (Vte) and resistance (Rte) were measured and the equivalent short-circuit current (Isc = Vte/Rte) was calculated. After serosal (s) and mucosal (m) addition of indomethacin (1 mumol/l) Isc was -71 +/- 11 (n = 118) microA/cm2. Amiloride (0.1 mmol/l, m) inhibited this current and reversed the polarity to +32 +/- 4 (n = 118) microA/cm2. In the presence of amiloride and indomethacin, prostaglandin E2 (1 mumol/l, s), known to induce Cl- secretion, generated an Isc of -143 +/- 8 (n = 92) microA/cm2. The arylaminobenzoate and Cl- channel blocker 5-nitro-2-(3-phenylpropylamino)-benzoate (NPPB) reduced Isc reversibly with a half-maximal inhibition (IC50) at approximately 0.35 mmol/l and 0.2 mmol/l for mucosal and serosal application respectively. To test whether the poor effect was caused by mucus covering the luminal surface, dose/response curves of the mucosal effect were repeated after several pretreatments. Acidic pH on the mucosal side reduced IC50 to approximately 0.1 mmol/l. A similar effect was observed after N-acetyl-L-cysteine (m) preincubation. Pretreatment with N-acetyl-L-cysteine (m) and carbachol (s), in order to exhaust mucus secretion, and L-homocysteine (m) were more effective and reduced IC50 to approximately 50 mumol/l. To test whether this effect of NPPB was caused by non-specific effects, the two enantiomers of 5-nitro-2-(+/-1-phenylethylamino)-benzoate were tested of which only the (+) form inhibited the Cl- conductance in the thick ascending limb of the loop of Henle (TAL).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在置于尤斯灌流小室的兔结肠中对芳基氨基苯甲酸酯进行了研究。测量了开路跨上皮电压(Vte)和电阻(Rte),并计算了等效短路电流(Isc = Vte/Rte)。在浆膜侧(s)和黏膜侧(m)加入吲哚美辛(1 μmol/L)后,Isc为-71±11(n = 118)μA/cm²。氨氯吡脒(0.1 mmol/L,m)抑制了该电流,并使极性反转至+32±4(n = 118)μA/cm²。在存在氨氯吡脒和吲哚美辛的情况下,已知可诱导氯离子分泌的前列腺素E2(1 μmol/L,s)产生了-143±8(n = 92)μA/cm²的Isc。芳基氨基苯甲酸酯和氯离子通道阻滞剂5-硝基-2-(3-苯丙基氨基)-苯甲酸酯(NPPB)分别在黏膜侧和浆膜侧应用时,以约0.35 mmol/L和0.2 mmol/L的半数最大抑制浓度(IC50)可逆地降低Isc。为了测试这种不良效应是否由覆盖管腔表面的黏液引起,在进行几次预处理后重复了黏膜效应的剂量/反应曲线。黏膜侧的酸性pH将IC50降低至约0.1 mmol/L。在N-乙酰-L-半胱氨酸(m)预孵育后观察到类似的效果。用N-乙酰-L-半胱氨酸(m)和卡巴胆碱(s)进行预处理以耗尽黏液分泌,以及L-高半胱氨酸(m)更有效,并将IC50降低至约50 μmol/L。为了测试NPPB的这种效应是否由非特异性效应引起,对5-硝基-2-(±1-苯乙氨基)-苯甲酸酯的两种对映体进行了测试,其中只有(+)形式抑制了亨氏袢厚升支(TAL)中的氯离子电导。(摘要截短于250字)

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