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麻醉犬心脏交感神经对去甲肾上腺素的神经元再摄取及二羟苯乙二醇的生成

Neuronal reuptake of norepinephrine and production of dihydroxyphenylglycol by cardiac sympathetic nerves in the anesthetized dog.

作者信息

Eisenhofer G, Smolich J J, Cox H S, Esler M D

机构信息

Baker Medical Research Institute, Prahran, Victoria, Australia.

出版信息

Circulation. 1991 Sep;84(3):1354-63. doi: 10.1161/01.cir.84.3.1354.

Abstract

BACKGROUND

Reuptake of norepinephrine by cardiac sympathetic nerves before and during two levels of electrical stimulation of the left ansa subclavia was estimated in anesthetized dogs from the cardiac production of dihydroxyphenylglycol (DHPG), the intraneuronal metabolite of norepinephrine.

METHODS AND RESULTS

The method depended on the effects of neuronal uptake blockade with desipramine on the cardiac production of [3H]DHPG from intravenously infused [3H]norepinephrine. The ratio of the desipramine-induced decrease in the cardiac extraction of [3H]norepinephrine to the production of [3H]DHPG was used to transform the cardiac production of DHPG from recaptured norepinephrine into a rate for norepinephrine reuptake. Cardiac spillover of norepinephrine into plasma increased from 49 +/- 12 to 205 +/- 40 and 451 +/- 118 pmol/min during sympathetic activation. Cardiac DHPG production increased from 108 +/- 18 to 166 +/- 34 and 240 +/- 47 pmol/min. Desipramine decreased resting cardiac DHPG production by 20% and completely blocked the stimulation-induced increase. Thus, most (80%) cardiac DHPG produced at rest was derived from norepinephrine leaking from storage vesicles. This amount remained constant, and that derived from recaptured norepinephrine increased during sympathetic activation. The cardiac extraction of [3H]norepinephrine (126,000 dpm/min) and production of [3H]DHPG (3,790 dpm/min) were decreased by 55-57% after desipramine. Thus, only 3% of the norepinephrine recaptured by cardiac sympathetic nerves appeared in plasma as DHPG. The remainder was sequestered into storage vesicles (more than 94%) or ultimately formed metabolites other than DHPG (less than 3%). Reuptake of norepinephrine by cardiac sympathetic nerves was 1,188 +/- 476 pmol/min and increased in parallel with cardiac norepinephrine spillover to 4,182 +/- 1,982 and 6,594 +/- 2,241 pmol/min during sympathetic stimulation.

CONCLUSIONS

Of the norepinephrine released by cardiac sympathetic nerves, 16-fold more was recaptured than entered plasma. Combined estimation of norepinephrine reuptake and spillover offers an approach to assess the efficiency of neuronal reuptake in disorders of cardiac function.

摘要

背景

在麻醉犬中,通过测定去甲肾上腺素的神经元内代谢产物二羟苯乙二醇(DHPG)在心脏中的生成量,来评估左锁骨下襻两层电刺激前后心脏交感神经对去甲肾上腺素的再摄取情况。

方法与结果

该方法依赖于地昔帕明对神经元摄取的阻断作用对静脉注射[3H]去甲肾上腺素后心脏中[3H]DHPG生成的影响。用地昔帕明引起的[3H]去甲肾上腺素心脏摄取减少量与[3H]DHPG生成量的比值,将从再摄取的去甲肾上腺素生成的心脏DHPG量转化为去甲肾上腺素再摄取速率。在交感神经激活过程中,心脏去甲肾上腺素向血浆中的溢出量从49±12增加到205±40和451±118 pmol/分钟。心脏DHPG生成量从108±18增加到166±34和240±47 pmol/分钟。地昔帕明使静息时心脏DHPG生成量减少20%,并完全阻断刺激诱导的增加。因此,静息时产生的大部分(80%)心脏DHPG来自于从储存囊泡泄漏的去甲肾上腺素。该量保持恒定,而来自再摄取的去甲肾上腺素的量在交感神经激活期间增加。地昔帕明作用后,[3H]去甲肾上腺素的心脏摄取量(126,000 dpm/分钟)和[3H]DHPG的生成量(3,790 dpm/分钟)减少了55 - 57%。因此,心脏交感神经再摄取的去甲肾上腺素中只有3%以DHPG的形式出现在血浆中。其余的被隔离到储存囊泡中(超过94%)或最终形成除DHPG以外的代谢产物(少于3%)。心脏交感神经对去甲肾上腺素的再摄取量为1,188±476 pmol/分钟,并在交感神经刺激期间与心脏去甲肾上腺素溢出量平行增加至4,182±1,982和6,594±2,241 pmol/分钟。

结论

心脏交感神经释放的去甲肾上腺素中,被再摄取的量比进入血浆的量多16倍。联合评估去甲肾上腺素再摄取和溢出为评估心脏功能障碍中神经元再摄取效率提供了一种方法。

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