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美沙酮在体外可抑制5-羟色胺和去甲肾上腺素摄取进入大鼠脑突触体和突触小泡,但在体内则无此作用。

Methadone inhibits serotonin and norephinephrine uptake into rat brain synaptosomes and synaptic vesicles in vitro but not in vivo.

作者信息

Slotkin T A, Seidler F J, Whitmore W L

出版信息

Eur J Pharmacol. 1978 Jun 15;49(4):357-62. doi: 10.1016/0014-2999(78)90309-6.

Abstract

Methadone in vitro inhibited biogenic amine uptake into synaptosomes isolated from rat whole brain; the IC50 for inhibition of serotonin uptake was between 0.1 and 1 micron, and for norepinephrine uptake, 10 micron when the serotonin or norepinephrine concentration was 0.05 micron. Methadone in vitro also inhibited uptake of norepinephrine into rat brain synaptic vesicles to the same extent that it inhibited synaptosomal norepinephrine uptake. In all cases, all cases, morphine in vitro was much less effective in blocking uptake. However, in vivo acute or chronic administration of methadone to rats failed to cause inhibition of serotonin or norepinephrine uptakes in synaptosomes isolated from the brains of treated rats, nor was inhibition of vesicular norepinephrine uptake produced. Amine uptake in situ also was unaffected by methadone administration, as evidenced by normal incorporation of intracisternally administered 3H-serotonin into synaptic endings. These data show that inhibition of synaptosomal and vesicular biogenic amine uptake by methadone in vitro is probably not a major determinant of the alterations in biogenic amine turnover caused by methadone administration. Thus, results obtained with platelets and adrenomedullary chromaffin vesicles, in which methadone administration does cause effective inhibition of amine uptake in vivo, cannot be extended to the central nervous system.

摘要

美沙酮在体外可抑制从大鼠全脑分离出的突触体摄取生物胺;当血清素或去甲肾上腺素浓度为0.05微米时,抑制血清素摄取的IC50在0.1至1微米之间,抑制去甲肾上腺素摄取的IC50为10微米。美沙酮在体外还能抑制去甲肾上腺素摄取到大鼠脑突触小泡中的程度与它抑制突触体去甲肾上腺素摄取的程度相同。在所有情况下,吗啡在体外阻断摄取的效果要差得多。然而,对大鼠进行美沙酮的体内急性或慢性给药未能抑制从经处理大鼠脑部分离出的突触体中血清素或去甲肾上腺素的摄取,也未产生对突触小泡去甲肾上腺素摄取的抑制。原位胺摄取也不受美沙酮给药的影响,脑池内注射的3H-血清素正常掺入突触末梢就证明了这一点。这些数据表明,美沙酮在体外对突触体和突触小泡生物胺摄取的抑制可能不是美沙酮给药引起生物胺周转改变的主要决定因素。因此,在血小板和肾上腺髓质嗜铬小泡中获得的结果(在这些实验中,美沙酮给药确实会在体内有效抑制胺摄取)不能推广到中枢神经系统。

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