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抗生素四环素对大鼠皮层去甲肾上腺素能腺苷酸环化酶及苯丙胺诱发的多动的抑制作用。

Inhibition by antibiotic tetracyclines of rat cortical noradrenergic adenylate cyclase and amphetamine-induced hyperactivity.

作者信息

Kofman O, Klein E, Newman M, Hamburger R, Kimchi O, Nir T, Shimon H, Belmaker R H

机构信息

Beer Sheva Mental Health Centre, Ben Gurion University of the Negev, Israel.

出版信息

Pharmacol Biochem Behav. 1990 Nov;37(3):417-24. doi: 10.1016/0091-3057(90)90006-4.

Abstract

Two antibiotic tetracyclines, demeclocycline (DMC) and minocycline, share several biochemical and behavioral properties with lithium (Li). DMC inhibited both noradrenaline- and chloradenosine-sensitive cyclic AMP accumulation in rat cerebral cortical slices both in vitro and ex vivo following two weeks of chronic dietary treatment. Minocycline, a lipophilic tetracycline, produced similar results in vitro. Both DMC and minocycline reduced open-field activity levels in rats following acute treatment, four hours prior to testing. Moreover, both drugs inhibited amphetamine-induced hyperactivity in the open field. Chronic treatment with 0.4% and 0.8% dietary DMC for two weeks attenuated amphetamine hyperactivity without affecting baseline activity levels in the open field. Neither DMC nor minocycline attenuated apomorphine-induced stereotypy at doses that attenuated amphetamine hyperactivity, a profile which is similar to that of lithium. Unlike lithium, however, DMC did not reverse reserpine-induced hypoactivity.

摘要

两种抗生素四环素,即地美环素(DMC)和米诺环素,与锂(Li)具有一些生化和行为特性。在经过两周的慢性饮食治疗后,无论是在体外还是体内,DMC均能抑制大鼠大脑皮质切片中去甲肾上腺素和氯腺苷敏感的环磷酸腺苷(cAMP)积累。亲脂性四环素米诺环素在体外产生了类似的结果。在测试前四小时进行急性治疗后,DMC和米诺环素均降低了大鼠在旷场试验中的活动水平。此外,两种药物均抑制了苯丙胺在旷场中引起的多动。用0.4%和0.8%的饮食DMC进行两周的慢性治疗可减弱苯丙胺引起的多动,而不影响旷场试验中的基线活动水平。在减弱苯丙胺多动的剂量下,DMC和米诺环素均未减弱阿扑吗啡引起的刻板行为,这一特征与锂相似。然而,与锂不同的是,DMC并未逆转利血平引起的活动减退。

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