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甲硫氨酸脑啡肽和吗啡肽调节椎实螺中枢神经系统中γ-氨基丁酸诱导的内向电流。

Met-enkephalin and morphiceptin modulate a GABA-induced inward current in the CNS of Lymnaea stagnalis L.

作者信息

Rózsa K S, Rubakhin S S, Szücs A, Stefano G B

机构信息

Balaton Limnological Research Institute of the Hungarian Academy of Sciences, Hungary.

出版信息

Gen Pharmacol. 1996 Dec;27(8):1337-45. doi: 10.1016/s0306-3623(96)00147-4.

Abstract
  1. The interaction between GABA and opioid peptides (met-enkephalin and morphiceptin) was studied on the identified, isolated and internally perfused neurons of Lymnaea stagnalis L. (Gastropoda, Basommatophora). 2. GABA (10(-7)-10(-5)M) activated a Cl-dependent inward current with about -20 mV equilibrium potential. Slow and fast GABA-induced inward currents were recorded with different kinetic parameters in distinct identified neurons. 3. Both types of GABA-induced inward currents were reduced or blocked by met-enkephalin (10(-7)-10(-5)M) and morphiceptin (10(-7)-10(-5)M) in a dose-dependent manner. GABA-activated fast inward current was modulated in a biphasic way in some neurons. Opioid reduction of the GABA-activated slow inward current was reversible, whereas the fast current was not. 4. The reversible inhibition of the GABA-induced slow inward current produced by met-enkephalin or morphiceptin was naloxone (10(-5)-10(-4)M)-sensitive, whereas the irreversible block of the fast GABA response was not antagonised by naloxone. Some additive effects between GABA and the peptides were also noted. 5. The modulatory effect of the opioid peptides on the GABA response altered the peak current, the time-to-peak and inactivation time-course of the GABA-induced current. 6. Thus, the identified, isolated and internally perfused neurons of Lymnaea stagnalis L. provide a useful model for studying postsynaptic mechanisms of interaction between GABA and opioid peptides. This interaction is a phenomenon of evolutionary significance because of it is also found in mammals.
摘要
  1. 研究了γ-氨基丁酸(GABA)与阿片肽(甲硫氨酸脑啡肽和吗啡肽)在静水椎实螺(腹足纲,基眼目)已鉴定、分离并进行内部灌流的神经元上的相互作用。2. GABA(10⁻⁷ - 10⁻⁵M)激活了一种平衡电位约为 -20 mV的氯离子依赖性内向电流。在不同的已鉴定神经元中,记录到了具有不同动力学参数的慢速和快速GABA诱导的内向电流。3. 两种类型的GABA诱导的内向电流均被甲硫氨酸脑啡肽(10⁻⁷ - 10⁻⁵M)和吗啡肽(10⁻⁷ - 10⁻⁵M)以剂量依赖性方式降低或阻断。在一些神经元中,GABA激活的快速内向电流以双相方式被调节。阿片肽对GABA激活的慢速内向电流的降低是可逆的,而快速电流则不可逆。4. 甲硫氨酸脑啡肽或吗啡肽对GABA诱导的慢速内向电流的可逆抑制对纳洛酮(10⁻⁵ - 10⁻⁴M)敏感,而快速GABA反应的不可逆阻断则不受纳洛酮拮抗。还注意到GABA与这些肽之间存在一些相加作用。5. 阿片肽对GABA反应的调节作用改变了GABA诱导电流的峰值电流、峰值时间和失活时间进程。6. 因此,静水椎实螺已鉴定、分离并进行内部灌流的神经元为研究GABA与阿片肽之间突触后相互作用机制提供了一个有用的模型。这种相互作用是一种具有进化意义的现象,因为在哺乳动物中也发现了这种现象。

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