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麻醉兔体内去甲肾上腺素的分泌速率:肾上腺素的促进作用。

The noradrenaline rate in the anaesthetized rabbit: facilitation by adrenaline.

作者信息

Majewski H, Hedler L, Starke K

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1982 Oct;321(1):20-7. doi: 10.1007/BF00586343.

Abstract
  1. 3H-Noradrenaline was infused intravenously into pentobarbitone anaesthetized rabbits to reach a steady-state plasma 3H-noradrenaline level, from which the noradrenaline plasma clearance was calculated. The plasma level of endogenous noradrenaline was determined simultaneously and the rate of noradrenaline release was then derived. 2. Pargyline, amezinium, desipramine and guanethidine all reduced the noradrenaline plasma clearance. The noradrenaline release rate was decreased by desipramine, guanethidine and clonidine. 3. Adrenaline (6 nmol/kg i.v. twice) enhanced the noradrenaline release rate by 53%. This effect was apparent after the plasma adrenaline has returned to basal levels. The adrenaline levels in sympathetically innervated tissues were elevated at this time. 4. When the rabbits were pretreated with either propranolol HCl (1 mg/kg i.p.) to block beta-adrenoceptors, or desipramine HCl (1 mg/kg i.v.) to block neuronal uptake, the facilitatory effect of adrenaline was abolished. Noradrenaline (6 nmol/kg i.v. twice) had no effect on the noradrenaline release rate. 5. These findings suggest that if the sympathetic transmitter stores contain sufficient adrenaline neuronally released adrenaline may modulate noradrenaline release in vivo by activating facilitatory presynaptic beta-adrenoceptors.
摘要
  1. 将3H-去甲肾上腺素静脉注入戊巴比妥麻醉的兔体内,以达到稳态血浆3H-去甲肾上腺素水平,据此计算去甲肾上腺素的血浆清除率。同时测定内源性去甲肾上腺素的血浆水平,进而推算出去甲肾上腺素的释放速率。2. 优降宁、阿美铵、地昔帕明和胍乙啶均降低了去甲肾上腺素的血浆清除率。地昔帕明、胍乙啶和可乐定降低了去甲肾上腺素的释放速率。3. 肾上腺素(6 nmol/kg静脉注射,共两次)使去甲肾上腺素释放速率提高了53%。在血浆肾上腺素恢复到基础水平后,这种效应仍然明显。此时,交感神经支配组织中的肾上腺素水平升高。4. 当兔预先用盐酸普萘洛尔(1 mg/kg腹腔注射)阻断β-肾上腺素受体,或用盐酸地昔帕明(1 mg/kg静脉注射)阻断神经元摄取时,肾上腺素的促进作用被消除。去甲肾上腺素(6 nmol/kg静脉注射,共两次)对去甲肾上腺素释放速率没有影响。5. 这些发现表明,如果交感神经递质储存中有足够的肾上腺素,神经元释放的肾上腺素可能通过激活突触前促进性β-肾上腺素受体在体内调节去甲肾上腺素的释放。

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