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细胞内和细胞外pH值对离体大鼠门静脉收缩作用的比较。

A comparison of the effects of intracellular and extracellular pH on contraction in isolated rat portal vein.

作者信息

Taggart M, Austin C, Wray S

机构信息

Physiological Laboratory, University of Liverpool.

出版信息

J Physiol. 1994 Mar 1;475(2):285-92. doi: 10.1113/jphysiol.1994.sp020069.

Abstract
  1. The effects of changes in extracellular and intracellular pH on spontaneous contractile activity in isolated rat portal vein have been investigated. 2. Small strips of portal vein were loaded with the pH-sensitive fluorophore carboxy-SNARF and intracellular pH (pHi) and contraction were measured simultaneously at 37 degrees C. The tissue was superfused with oxygenated, Hepes-buffered solutions at pH 7.4. Intracellular pH was altered by isosmotic substitution of weak acids or bases. External pH (pHo) was altered by addition of strong acid or base to the solution. 3. The mean resting value of pHi was 7.06 +/- 0.03 (n = 28). Alteration of pHi led to changes in spontaneous activity. Addition of butyrate (20 mM) reduced pHi by 0.18 +/- 0.01 pH units (n = 8). Decreasing pHi produced an early, brief increase in contractile activity followed by a longer lasting decrease or even abolition of contraction. 4. Addition of 20 mM trimethylamine or NH4Cl increased pHi by around 0.2 pH units and produced an early transient decrease in contractile activity followed by a later maintained increase, both in frequency and magnitude. Removal of base produced a rapid rebound decrease in pHi which was associated with a further transient increase in contractile activity followed by decreased activity. The effects of base on both pHi and contraction were concentration dependent over the range investigated (2.5-30 mM). 5. Alteration of pHo produced a change in pHi in the portal vein. The pHi change was rapid compared to other non-vascular cells (about 1 min to half-maximal response).(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 研究了细胞外和细胞内pH变化对离体大鼠门静脉自发收缩活性的影响。2. 将门静脉小条加载pH敏感荧光团羧基-SNARF,并在37℃同时测量细胞内pH(pHi)和收缩情况。组织用pH 7.4的含氧、Hepes缓冲溶液进行灌流。通过等渗替代弱酸或弱碱来改变细胞内pH。通过向溶液中添加强酸或强碱来改变细胞外pH(pHo)。3. pHi的平均静息值为7.06±0.03(n = 28)。pHi的改变导致自发活性发生变化。添加丁酸盐(20 mM)使pHi降低0.18±0.01个pH单位(n = 8)。降低pHi会导致收缩活性早期短暂增加,随后是持续时间更长的降低甚至收缩消失。4. 添加20 mM三甲胺或氯化铵使pHi升高约0.2个pH单位,并导致收缩活性早期短暂降低,随后在频率和幅度上出现后期持续增加。去除碱会使pHi迅速反弹降低,这与收缩活性进一步短暂增加随后降低有关。在所研究的浓度范围(2.5 - 30 mM)内,碱对pHi和收缩的影响均呈浓度依赖性。改变pHo会使门静脉中的pHi发生变化。与其他非血管细胞相比,pHi变化迅速(约1分钟达到最大反应的一半)。(摘要截短至250字)

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