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[河豚毒素对家兔减压神经自然放电活动的局部麻醉作用]

[The local anesthetic effect of tetrodotoxin on the natural spike activity of the depressor nerve in rabbits].

作者信息

Lipfert P, Beyer G, Lömm M

机构信息

Abteilung für Experimentelle Anaesthesiologie, Universität Düsseldorf.

出版信息

Reg Anaesth. 1989 Jul;12(4):69-75.

PMID:2772276
Abstract

Tetrodotoxin (TTX) has been presented as an ultra-long-acting local anesthetic. Because its duration of action on myelinated nerve fibers of warm-blooded animals is unknown the effect of TTX on natural spike activity (A-delta fibers) of rabbit aortic nerve in vivo was studied. In 13 animals, a segment of the aortic nerve was placed in a perfusion chamber and exposed to increasing concentrations of TTX (n = 8) and, for comparison, of procaine (n = 8), which like TTX has a high pka. Total nerve activity and its change as related to drug concentrations was recorded continuously (concentration effect curves). The half-lives (t1/2) of onset time after drug administration and recovery following drug washout were also determined. TTX blocked nerve activity in a concentration-related manner, as did procaine; however, the potency of TTX (EC50 = 3.3 +/- 0.8.10(-9), cm = 1.3 +/- 0.4.10(-8) mol/l) was about 50,000 times higher than that of procaine (EC50 = 1.6 +/- 0.2.10(-4), cm = 2.5 4/- 0.3.10(-4) mol/l). Onset time did not differ statistically (p = 0.08) between TTX (t1/2 = 3.5 +/- 0.4 min) and procaine (t1/2 = 2.2 +/- 0.5 min). Most importantly, TTX block could not be reversed within 1-5 h of drug washout (n = 5) or was reversed incompletely (13%, 66%, and 90% of control activity) with t1/2 16 to 21 min. In contrast, all the procaine-blocked nerves recovered completely (t1/2 = 3.0 +/- 0.4 min). TTX blocks myelinated A-delta fibers of warm-blooded animals with lower concentrations and for a longer time than nonmyelinated fibers.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

河豚毒素(TTX)已被视作一种超长效局部麻醉剂。由于其对温血动物有髓神经纤维的作用持续时间未知,因此研究了TTX对兔主动脉神经在体自然锋电位活动(A-δ纤维)的影响。在13只动物中,将一段主动脉神经置于灌注室,并暴露于浓度递增的TTX(n = 8)以及作为对照的普鲁卡因(n = 8)中,普鲁卡因与TTX一样具有高pKa值。连续记录总神经活动及其与药物浓度相关的变化(浓度效应曲线)。还测定了给药后起效时间的半衰期(t1/2)以及药物洗脱后的恢复半衰期。TTX与普鲁卡因一样,以浓度相关的方式阻断神经活动;然而,TTX的效力(EC50 = 3.3 +/- 0.8×10⁻⁹,cm = 1.3 +/- 0.4×10⁻⁸mol/L)比普鲁卡因(EC50 = 1.6 +/- 0.2×10⁻⁴,cm = 2.5 +/- 0.3×10⁻⁴mol/L)高约50000倍。TTX(t1/2 = 3.5 +/- 0.4分钟)和普鲁卡因(t1/2 = 2.2 +/- 0.5分钟)之间的起效时间在统计学上无差异(p = 0.08)。最重要的是,在药物洗脱1 - 5小时内,TTX阻断无法逆转(n = 5),或者在t1/2为16至21分钟时仅部分逆转(恢复至对照活动的13%、66%和90%)。相比之下,所有被普鲁卡因阻断的神经均完全恢复(t1/2 = 3.0 +/- 0.4分钟)。与无髓纤维相比,TTX以更低的浓度和更长的时间阻断温血动物的有髓A-δ纤维。(摘要截短于250字)

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