Kuba K, Kumamoto E
J Physiol. 1986 May;374:515-30. doi: 10.1113/jphysiol.1986.sp016095.
Long-term potentiation (l.t.p.) of transmitter release induced by adrenaline in bull-frog sympathetic ganglia was studied using intracellular recording techniques. The quantal content of the fast excitatory post-synaptic potentials (fast e.p.s.p.s: evoked by the nicotinic action of acetylcholine) was potentiated for more than several hours after treatment with adrenaline (1-100 microM). A similar l.t.p. of quantal content was produced consistently by isoprenaline (10 microM) and only in a certain fraction of cells by dopamine (10 microM). The l.t.p. induced by adrenaline (10 microM) was blocked by a beta-antagonist, propranolol (1 microM), but not by an alpha-antagonist, phenoxybenzamine (1 microM). Dibutyryl adenosine 3',5'-phosphate (dibutyryl cyclic AMP) (0.8-1.0 mM), adenosine 3',5'-phosphate (cyclic AMP) (4 mM), 3-isobutyl-1-methylxanthine (10 microM), caffeine (1-2 mM), and cholera toxin (2 micrograms ml-1) applied for 20-30 min, all caused the l.t.p. of quantal content. By contrast, adenosine 5'-phosphate (AMP) (4 mM) and adenosine (4 mM) had no potentiating action. Treatment of the ganglion with adrenaline (2.5-160 microM) or dibutyryl cyclic AMP (4 mM) for 15-30 min resulted in the l.t.p. of the frequency of miniature e.p.s.p.s. The l.t.p. of quantal content induced by adrenaline was markedly suppressed by lowering temperature from 20-25 degrees C to 11-13 degrees C, and blocked by dibutyryl guanosine 3',5'-phosphate (dibutyryl cyclic GMP) (100 microM) consistently when applied together, but inconsistently when given after adrenaline. The post-synaptic sensitivity to acetylcholine was unchanged for at least 1 h after exposure to adrenaline (2.5-160 microM) or dibutyryl cyclic AMP (0.8-4 mM). It can be concluded that adrenaline produces l.t.p. of transmitter release by activating a cyclic-AMP-dependent metabolic process through the activation of beta-adrenoceptors, and that this mechanism is presumably regulated by a process involving endogenous guanosine 3',5'-phosphate (cyclic GMP).
运用细胞内记录技术,研究了肾上腺素在牛蛙交感神经节中诱导的递质释放的长期增强效应(LTP)。在用肾上腺素(1 - 100微摩尔)处理后,快速兴奋性突触后电位(快速EPSP:由乙酰胆碱的烟碱样作用诱发)的量子含量增强了几个多小时。异丙肾上腺素(10微摩尔)能持续产生类似的量子含量的LTP,而多巴胺(10微摩尔)仅在一定比例的细胞中产生这种效应。肾上腺素(10微摩尔)诱导的LTP被β拮抗剂普萘洛尔(1微摩尔)阻断,但不被α拮抗剂酚苄明(1微摩尔)阻断。二丁酰腺苷3',5'-磷酸(二丁酰环磷酸腺苷)(0.8 - 1.0毫摩尔)、腺苷3',5'-磷酸(环磷酸腺苷)(4毫摩尔)、3 - 异丁基 - 1 - 甲基黄嘌呤(10微摩尔)、咖啡因(1 - 2毫摩尔)和霍乱毒素(2微克/毫升)作用20 - 30分钟,均能引起量子含量的LTP。相比之下,腺苷5'-磷酸(AMP)(4毫摩尔)和腺苷(4毫摩尔)没有增强作用。用肾上腺素(2.5 - 160微摩尔)或二丁酰环磷酸腺苷(4毫摩尔)处理神经节15 - 30分钟,可导致微小EPSP频率的LTP。将温度从20 - 25摄氏度降至11 - 13摄氏度,能显著抑制肾上腺素诱导的量子含量的LTP,当同时应用二丁酰鸟苷3',5'-磷酸(二丁酰环磷酸鸟苷)(100微摩尔)时可将其阻断,但在肾上腺素作用后给予则阻断效果不一致。暴露于肾上腺素(2.5 - 160微摩尔)或二丁酰环磷酸腺苷(0.8 - 4毫摩尔)后,突触后对乙酰胆碱的敏感性至少1小时内未发生变化。可以得出结论,肾上腺素通过激活β肾上腺素能受体来激活依赖环磷酸腺苷的代谢过程,从而产生递质释放的LTP,并且该机制可能受涉及内源性鸟苷3',5'-磷酸(环磷酸鸟苷)的过程调控。