yohimbine

[joʊ'hɪmˌbi:n][jəʊ'hɪmbi:n]

n.育亨宾(从茜草科柯楠树皮提炼出的生物碱),壮阳碱

  • Arousal Effect of Tolazoline and Yohimbine on Jing Song Ling and Bao Ding Ning & Induced General Anaesthesia in Sheep

    妥拉苏林和 亨宾对静松灵及保定宁麻醉羊的催醒实验

  • Using tail-flick test and writhing test the effect of intrathecal injection ( IT ) of yohimbine at different concentrations on the analgesic action of ketamine was observed .

    用甩尾法和扭体法观察鞘内注射不同浓度的 亨宾对氯胺酮镇痛作用的影响。

  • HA and the effects of pretreatment with α 2 receptor selective antagonist yohimbine ( YOH ) into the peripheral vein on the responses of CBR to HA .

    选择性α2受体拮抗剂 亨宾(YOH)对CBR的影响。

  • Homology Modeling and Docking Studies of the α 2A-adrenergic Receptor

    α2A-肾上腺素受体的同源模建及与 Yohimbine的对接 研究

  • Determination of yohimbine hydrochloride and its tablets with HPLC

    HPLC测定盐酸 亨宾及其片剂的含量

  • Effects of clonidine and yohimbine on electroacupuncture analgesia

    可乐宁和 亨宾对电针镇痛的影响

  • Radioligand Binding Analysis of Adrenergic Receptor Subtypes on the Rat Liver Plasma Membrane with ( ~ 3H ) - prazosin and ( ~ 3H ) - yohimbine Subtypes of CNV are also existed .

    采用~3H-哌唑嗪、~3H-育 亨宾结合分析法测定鼠肝中α1、α2受体此外还存在脉络膜新生血管的 特殊 形式

  • With reference to the related foreign literatures we decided to put the synthesis of yohimbine on our schedule and design routine .

    课题 在参照国外文献报道的基础上,确定 亨宾合成研究课题,并设计了 整体的合成路线。

  • Pretreatment with phentolamine prazosin but not yohimbine attenuated icv SP-induced cardiovascular responses compared with controls ( P < 0.05 ) .

    酚妥拉明或哌唑嗪预处理可显著减弱脑室注射SP引起心血管增强效应(P<0.05),但 亨宾预处理对注射SP引起的心血管效应无明显影响(P<0.05)。

  • The resulting thermograms indicated that yohimbine hydrochloride had a high activation energy and a good stability ;

    实验表明:盐酸 亨宾具有较高的活化能,稳定性较好;

  • Yohimbine ( 0.5 ~ 5 mg / kg sc ) exhibited an antagonistic action on the inhibitory effect of clonidine on the gastrointestinal propulsion and defecation in mice .

    亨宾(0.5~5mg/kg,sc)剂量依赖式地拮抗可乐定对小鼠胃肠推进运动及排便的抑制作用。

  • The antagonism of intrathecal injection of yohimbine on the analgesia by ketamine

    鞘内注射 亨宾拮抗氯胺酮的镇痛作用

  • Yohimbine has even been shown to increase the force and the amount of ejaculate enhancing the male orgasm .

    亨宾能够提高男性射精时的力度和数量,从而增强男性的快感。

  • Methods The antidepressant effect of TT was examined by mice forced swimming test ( FST ) learned helplessness ( LH ) experiment chronic mild stress ( CMS ) model yohimbine induced lethality test and 5-HTP induced head-twitches test .

    方法采用小鼠强迫游泳实验,获得性无助实验,慢性温和应激模型, 亨宾毒性增强实验以及5-羟色胺酸诱导甩头实验等多种动物模型考察TT的抗实验性抑郁作用及其可能的机制。

  • But yohimbine could not antagonize the central hypotensive action of GABA while picrotoxin could entirely block it .

    但是 亨宾不能阻断侧脑室注射GABA的中枢降压作用,而苦味毒则能完全阻断其降压效应。

  • The contractions uere enhanced after blocking of presynaptic a receptors with yohimbine .

    亨宾阻断突触前膜x2受体后。

  • Cocaine and yohimbine increased the release of NE from artery strips probably through a different course of action .

    可卡因和 亨宾通过不同的作用途径使动脉条释放NE增加。

  • Yohimbine α 2 antagonist blocked the spontaneous discharges of C ( 8 / 41 ) and A δ ( 22 / 79 ) units whereas clonidine increased the discharge frequencies of these units .

    在具有自发放电的C( 841)和Aδ(2279)单位中,α2受体拮抗剂 亨宾 阻断这些单位的自发电活动,而可乐定则使这些单位的放电频率增加;

  • AIM : To observe the influences of propofol anesthesia on the release of noradrenaline ( NA ) and α 2 NA receptor inhibitor yohimbine in rat hippocampus so as to identify the mechanisms of central noradrenaline in propofol anesthesia .

    目的:观察大鼠异丙酚麻醉与中枢神经系统海马去甲基肾上腺素(NA)的释放以及α2NA受体抑制剂 之间 相互 关系,探讨中枢性NA机制在异丙酚麻醉中发生的作用。

  • TT ( 50 mg · kg-1 ig qd × 14 d ) enhanced the mortality of mice after administration of yohimbine for 4 h and distinctly increased the head-twitch number in the 5-HTP induced head-twitches test .

    TT(50mg·kg-1,qd×14d)可提高 亨宾给药后4h的小鼠死亡率;并且显著增加5-羟色胺酸诱导小鼠的甩头次数。

  • Methods The antidepressant effects of Bioactive compounds from entomogenous fungi was examined on the chronic unpredictable stress test yohimbine induced lethality test and 5-HTP induced head-twitches test .

    方法采用未预知的慢性应激实验、 亨宾毒性实验、5羟色胺酸诱导甩头实验等多种模型研究BCEF抗实验性抑郁作用及可能的作用机制。