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大鼠离体肛尾肌对来自东亚钳蝎毒液的一种新毒素(马卡毒素I)的肾上腺素能和一氧化氮能反应。

Adrenergic and nitrergic responses of the rat isolated anococcygeus muscle to a new toxin (makatoxin I) from the venom of the scorpion Buthus martensi Karsch.

作者信息

Gong J P, Gwee M C, Gopalakrishnakone P, Kini R M, Chung M C

机构信息

Department of Anatomy, Faculty of Medicine, National University of Singapore, Singapore.

出版信息

J Auton Pharmacol. 1997 Apr;17(2):129-35. doi: 10.1046/j.1365-2680.1997.00448.x.

Abstract
  1. Makatoxin I (MkTx I) is a new toxin purified from the venom of the scorpion Buthus martensi Karsch. Contractile (excitatory, adrenergic) and relaxant (inhibitory, nitrergic) responses of the rat isolated anococcygeus muscle (Acm) to MkTx I were investigated. 2. MkTx I (0.28 microM) produced a rapid and very marked rise in the tone of the Acm which then gradually wanted to the control baseline. Phentolamine (5 microM), guanethidine (5 microM), tetrodotoxin (2 microM) and reserpine pretreatment in vivo (5 mg kg-1 s.c. at 24 hr and 5 mg kg-1 i.p. at 3 h) completely blocked the contractile responses of the Acm to MkTx I. The responses to noradrenaline (NA) were blocked by phentolamine, but were potentiated by guanethidine. 3. MkTx I (0.28 microM) also marked and rapidly relaxed the tone of the carbachol (CCh; 3 microM), precontracted Acm. The addition of sodium nitroprusside (SNP; 1 microM) also produced a marked and rapid relaxation of the Acm. TTx (2 microM) or NG-nitro-L-arginine methylester (L-NAME, 50 microM) markedly inhibited the relaxant responses of the Acm to field stimulation (FS) as well as to MkTx I, but not the responses to SNP. 4. Therefore, the contractile responses of the rat anococcygeus muscle to MkTx I can be attributed to the release of transmitter NA on postjunctional alpha-adrenoceptors, whereas the relaxant responses of the Acm to MkTx I involve the release of nitric oxide as the neurotransmitter which, presumably, results in the activation of the enzyme guanylate cyclase leading to relaxation of the muscle.
摘要
  1. 马卡毒素I(MkTx I)是从东亚钳蝎毒液中纯化得到的一种新毒素。研究了大鼠离体尾骨肌(Acm)对MkTx I的收缩(兴奋性、肾上腺素能)和舒张(抑制性、一氧化氮能)反应。2. MkTx I(0.28微摩尔)使Acm的张力迅速且显著升高,随后逐渐恢复至对照基线。酚妥拉明(5微摩尔)、胍乙啶(5微摩尔)、河豚毒素(2微摩尔)以及体内利血平预处理(24小时皮下注射5毫克/千克,3小时腹腔注射5毫克/千克)可完全阻断Acm对MkTx I的收缩反应。对去甲肾上腺素(NA)的反应可被酚妥拉明阻断,但被胍乙啶增强。3. MkTx I(0.28微摩尔)也可显著且迅速地舒张由卡巴胆碱(CCh;3微摩尔)预收缩的Acm的张力。添加硝普钠(SNP;1微摩尔)也可使Acm显著且迅速地舒张。河豚毒素(2微摩尔)或N - 硝基 - L - 精氨酸甲酯(L - NAME,50微摩尔)可显著抑制Acm对场刺激(FS)以及对MkTx I的舒张反应,但不影响对SNP的反应。4. 因此,大鼠尾骨肌对MkTx I的收缩反应可归因于神经递质NA在突触后α - 肾上腺素能受体上的释放,而Acm对MkTx I的舒张反应涉及一氧化氮作为神经递质的释放,这大概会导致鸟苷酸环化酶的激活,从而使肌肉舒张。

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