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Yohimbine anxiogenesis in the elevated plus maze is disrupted by bilaterally disconnecting the bed nucleus of the stria terminalis from the central nucleus of the amygdala.育亨宾在高架十字迷宫中的焦虑诱导作用被双侧切断终纹床核与杏仁中央核的连接所破坏。
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本文引用的文献

1
Autonomic and psychic effects of yohimbine hydrochloride.盐酸育亨宾的自主神经及精神效应。
Psychopharmacologia. 1961;2:93-106. doi: 10.1007/BF00592678.
2
Partial agonist properties of rauwolscine and yohimbine for the inhibition of adenylyl cyclase by recombinant human 5-HT1A receptors.萝芙辛和育亨宾对重组人5-HT1A受体抑制腺苷酸环化酶的部分激动剂特性。
Biochem Pharmacol. 1993 Jun 9;45(11):2337-41. doi: 10.1016/0006-2952(93)90208-e.
3
Abnormal noradrenergic function in posttraumatic stress disorder.创伤后应激障碍中去甲肾上腺素能功能异常。
Arch Gen Psychiatry. 1993 Apr;50(4):266-74. doi: 10.1001/archpsyc.1993.01820160036003.
4
Presynaptic alpha 2-autoreceptors in brain cortex: alpha 2D in the rat and alpha 2A in the rabbit.大脑皮层中的突触前α2 自身受体:大鼠中的α2D 和兔子中的α2A。
Naunyn Schmiedebergs Arch Pharmacol. 1993 Jul;348(1):35-45. doi: 10.1007/BF00168534.
5
Endogenous noradrenaline activates alpha 2-adrenoceptors on serotonergic nerve endings in human and rat neocortex.内源性去甲肾上腺素激活人和大鼠新皮质中5-羟色胺能神经末梢上的α2-肾上腺素能受体。
J Neurochem. 1993 Aug;61(2):474-80. doi: 10.1111/j.1471-4159.1993.tb02148.x.
6
An assessment of the elevated X-maze for studying anxiety and anxiety-modulating drugs.用于研究焦虑及焦虑调节药物的高架十字迷宫评估。
J Pharmacol Toxicol Methods. 1993 Jun;29(3):129-38. doi: 10.1016/1056-8719(93)90063-k.
7
Pharmacologic and therapeutic applications of alpha 2-adrenoceptor subtypes.α2 -肾上腺素能受体亚型的药理及治疗应用
Annu Rev Pharmacol Toxicol. 1993;33:243-79. doi: 10.1146/annurev.pa.33.040193.001331.
8
Modulation of central noradrenergic function by RS-15385-197.RS-15385-197对中枢去甲肾上腺素能功能的调节作用
Br J Pharmacol. 1993 Feb;108(2):526-33. doi: 10.1111/j.1476-5381.1993.tb12835.x.
9
The pharmacology of RS-15385-197, a potent and selective alpha 2-adrenoceptor antagonist.强效选择性α2肾上腺素能受体拮抗剂RS-15385-197的药理学
Br J Pharmacol. 1993 Feb;108(2):516-25. doi: 10.1111/j.1476-5381.1993.tb12834.x.
10
Alpha 2-adrenoceptors: more subtypes but fewer functional differences.α2肾上腺素能受体:亚型更多但功能差异更少。
Trends Pharmacol Sci. 1994 Apr;15(4):119-23. doi: 10.1016/0165-6147(94)90048-5.

使用选择性拮抗剂地来夸明,对大鼠中α2肾上腺素能受体在育亨宾致焦虑效应中的作用进行重新评估。

A re-evaluation of the role of alpha 2-adrenoceptors in the anxiogenic effects of yohimbine, using the selective antagonist delequamine in the rat.

作者信息

Redfern W S, Williams A

机构信息

Department of Pharmacology, Syntex Research Centre (now Quintiles Scotland Ltd), Heriot-Watt University Research Park, Riccarton, Edinburgh.

出版信息

Br J Pharmacol. 1995 Oct;116(3):2081-9. doi: 10.1111/j.1476-5381.1995.tb16415.x.

DOI:10.1111/j.1476-5381.1995.tb16415.x
PMID:8640349
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1908953/
Abstract
  1. The acute behavioural effects of the alpha2-adrenoceptor antagonists, yohimbine, idazoxan and delequamine (RS-15385-197) were compared in two tests of exploratory behaviour in the rat, operated in tandem. These were the elevated X-maze test (5 min) and a modified holeboard test (12 min), which comprised a holeboard arena with a small roof in one corner as a 'refuge'. Rats were first placed into this corner, thus enabling measurements of initial emergence latency and the number of forays. The experiments were always done with a concomitant vehicle control group, with 10-12 rats per group, and with the treatment blinded. 2. In order to validate the tests, the effects of representatives of four classes of psychoactive agents were examined, viz. picrotoxin (anxiogenic), chlordiazepoxide (anxiolytic), (+)-amphetamine (stimulant) and diphenhydramine (sedative). The modified holeboard tended to be more sensitive than the measurement of total arm entries in the elevated X-maze at detecting drug effects on exploratory behaviour, but unlike the X-maze it could not clearly identify each class of agent. Thus, picrotoxin (5 mg kg(-1), i.p.) reduced total arm entries and open arm exploration in the X-maze (P<0.02) and suppressed most measures of activity in the holeboard (P<0.05); chlordiazepoxide (7.5 mg kg(-1), i.p.) increased total arm entries and open arm exploration (P<0.02) in the X-maze, without clear-cut effects in the holeboard; (+)-amphetamine (1 mg kg(-1), i.p.) had no significant effects in the X-maze, but increased most holeboard activities (P<0.05), and diphenhydramine (30 mg kg(-1), i.p.) reduced total arm entries in the X-maze (P<0.002) and hole exploration in the holeboard (P<0.05).
摘要
  1. 在两项同步进行的大鼠探索行为测试中,比较了α2 -肾上腺素能受体拮抗剂育亨宾、伊达唑新和地来夸明(RS - 15385 - 197)的急性行为效应。这两项测试分别是高架X迷宫测试(5分钟)和改良的洞板测试(12分钟),改良洞板测试的场地是一个洞板 arena,在一个角落有一个小屋顶作为“避难所”。大鼠首先被放置在这个角落,从而能够测量初始出现潜伏期和突袭次数。实验总是设置一个相应的溶剂对照组,每组10 - 12只大鼠,并且实验过程是双盲的。2. 为了验证这些测试,研究了四类精神活性药物代表物的效应,即苦味毒(致焦虑)、氯氮卓(抗焦虑)、(+)-苯丙胺(兴奋剂)和苯海拉明(镇静剂)。在检测药物对探索行为的影响方面,改良洞板测试往往比高架X迷宫中总臂进入次数的测量更敏感,但与X迷宫不同的是,它不能清晰地识别每一类药物。因此,苦味毒(5毫克/千克,腹腔注射)减少了X迷宫中的总臂进入次数和开放臂探索次数(P < 0.02),并抑制了洞板测试中的大多数活动指标(P < 0.05);氯氮卓(7.5毫克/千克,腹腔注射)增加了X迷宫中的总臂进入次数和开放臂探索次数(P < 0.02),在洞板测试中没有明显效果;(+)-苯丙胺(1毫克/千克,腹腔注射)在X迷宫中没有显著影响,但增加了洞板测试中的大多数活动(P < 0.05),苯海拉明(30毫克/千克,腹腔注射)减少了X迷宫中的总臂进入次数(P < 0.002)和洞板测试中的洞探索次数(P < 0.05)。