首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Comparison of the effects of caffeine and procaine on noradrenergic transmission in the guinea-pig mesenteric artery.
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Comparison of the effects of caffeine and procaine on noradrenergic transmission in the guinea-pig mesenteric artery.

机译:比较咖啡因和普鲁卡因对豚鼠肠系膜动脉中去甲肾上腺素能传递的影响。

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摘要

The effects of caffeine and procaine on noradrenergic transmission in the guinea-pig mesenteric artery were investigated by recording electrical responses of smooth muscle cells and by measuring the outflow of noradrenaline (NA) and 3,4-dihydroxyphenylglycol (DOPEG) induced by perivascular nerve stimulation. Caffeine possessed dual actions on the membrane, i.e., at low concentrations (2.5 X 10(-4)-5 X 10(-4)M), it hyperpolarized the membrane and decreased the membrane resistance and at high concentrations (over 2.5 X 10(-3)M) it depolarized the membrane and increased the membrane resistance. Procaine (over 10(-4)M) consistently depolarized the membrane and increased the membrane resistance. The amplitude of the excitatory junction potential (e.j.p.) produced by perivascular nerve stimulation was increased by low concentrations of procaine (2.5 X 10(-5)-10(-4)M) or high concentrations (10(-3)-5 X 10(-3)M) of caffeine and was decreased by low concentrations of caffeine (2.5 X 10(-5)-10(-4)M) or high concentrations of procaine (5 X 10(-4)-10(-3)M). Higher concentrations of caffeine (over 5 X 10(-3)M) induced a spike potential on the e.j.p., while higher concentrations of procaine (over 2.5 X 10(-3)M) inhibited the generation of e.j.ps. Facilitation of e.j.ps produced by repetitive stimulation of perivascular nerves remained unchanged by caffeine, while it was enhanced by procaine at any given concentration (caffeine 2.5 X 10(-4)-10(-3)M; procaine 10(-4)-10(-3)M). The membrane depolarization produced by exogenously applied NA (10(-5)M) was not blocked by pretreatment with procaine. Conduction velocity of perivascular nerve excitation remained unchanged by application of caffeine (up to 5 X 10(-3)M), and was reduced by application of procaine (over 2.5 X 10(-4)M). Outflow of NA during perivascular nerve stimulation remained unchanged by caffeine (10(-4)-3 X 10(-3)M), while it was enhanced by procaine (over 2.5 X 10(-4)M). The outflow of DOPEG was slightly reduced by caffeine (10(-3)-5 X 10(-3)M) and by lower concentrations of procaine (10(-4)-2.5 X 10(-4)M) but was not altered by higher concentrations of procaine (10(-3)-5 X 10(-3)M). It is concluded that in the guinea-pig mesenteric artery, high concentrations of caffeine (over 10(-3)M) increased the e.j.p. amplitude which might be due to an increase in membrane resistance of the smooth muscle cells. No marked effect of caffeine was observed on transmitter release from the nerve terminals. Procaine (over 2.5 X 10(-4)M) increased transmitter release from perivascular nerves and blocked the re-uptake mechanism of released NA.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:通过记录平滑肌细胞的电响应并通过测量血管周神经刺激引起的去甲肾上腺素(NA)和3,4-二羟基苯二醇(DOPEG)的流出,研究了咖啡因和普鲁卡因对豚鼠肠系膜中去甲肾上腺素能传递的影响。 。咖啡因对膜具有双重作用,即在低浓度(2.5 X 10(-4)-5 X 10(-4)M)下,咖啡因会使膜超极化并降低膜电阻,在高浓度下(超过2.5 X 10 (-3)M)使膜去极化并增加膜电阻。普鲁卡因(超过10(-4)M)始终使膜去极化并增加膜电阻。低浓度的普鲁卡因(2.5 X 10(-5)-10(-4)M)或高浓度的普鲁卡因(10(-3)-5 X)会增加血管周围神经刺激产生的兴奋性连接电位(ejp)的幅度咖啡因10(-3)M,低浓度咖啡因(2.5 X 10(-5)-10(-4)M)或高浓度普鲁卡因(5 X 10(-4)-10(- 3)M)。较高浓度的咖啡因(超过5 X 10(-3)M)会在e.j.p上产生尖峰电位,而较高浓度的普鲁卡因(超过2.5 X 10(-3)M)会抑制e.j.ps的产生。咖啡因对重复刺激血管周神经产生的ejps的促进作用保持不变,而咖啡因在任何给定浓度下都被普鲁卡因增强(咖啡因2.5 X 10(-4)-10(-3)M;普鲁卡因10(-4)- 10(-3)M)。普鲁卡因预处理不会阻止外源性应用NA(10(-5)M)产生的膜去极化作用。通过使用咖啡因(高达5 X 10(-3)M),血管周围神经兴奋的传导速度保持不变,而通过使用普鲁卡因(超过2.5 X 10(-4)M)降低了传导速度。咖啡因(10(-4)-3 X 10(-3)M)在血管周围神经刺激过程中产生的NA流出量保持不变,而普鲁卡因(超过2.5 X 10(-4)M)则增加了流出量。咖啡因(10(-3)-5 X 10(-3)M)和较低浓度的普鲁卡因(10(-4)-2.5 X 10(-4)M)可使DOPEG的流出量略有减少,但并未降低被较高浓度的普鲁卡因(10(-3)-5 X 10(-3)M)改变。结论是在豚鼠肠系膜动脉中,高浓度的咖啡因(超过10(-3)M)增加了e.j.p.。振幅可能是由于平滑肌细胞的膜阻力增加所致。没有观察到咖啡因对神经末梢释放递质的明显作用。普鲁卡因(超过2.5 X 10(-4)M)增加了从血管周围神经释放的递质并阻止了释放的NA的再摄取机制。(摘要截短为400字)

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