Suppr超能文献

调节成年和10日龄家兔颈动脉体多巴胺释放的自身受体机制。

Autoreceptor mechanism regulating carotid body dopamine release from adult and 10-day-old rabbits.

作者信息

Bairam A, Néji H, De-Grandpré P, Carroll J L

机构信息

Unité de Recherche en Périnatologie, Centre Hospitalier Universitaire de Québec, PQ, Canada.

出版信息

Respir Physiol. 2000 Mar;120(1):27-34. doi: 10.1016/s0034-5687(00)00092-x.

Abstract

Dopamine (DA) release (r) from the carotid body (CB) is thought to be modulated by feedback inhibition mediated by DA D2 autoreceptors. We tested the hypothesis that CB DAr is autoregulated in a concentration and age dependent manner. Using an in vitro CB infusion model [Bairam, A., Marchal. F., Cottet-Emard, J.M., Basson, H., Pequignot, J.M., Hascoet, J.M., Lahiri, S., 1996b. Effects of hypoxia on carotid body dopamine content and release in developing rabbits. J. Appl. Physiol. 80, 20-24.], we evaluated under unstimulated conditions the effects of 0.001, 0.01, 0.1, 1.0 and 10.0 microM of the specific DA D2 receptor antagonist domperidone on CB DAr in adult rabbits. In 10-day-old rabbit pups, concentrations of 0.01, 0.1, 1.0 microM were studied. In adult CBs, domperidone increased DAr in a concentration-dependent manner. DAr (pmol/h) was significantly greater compared to control (without domperidone) starting at a domperidone concentration of 0.1 microM (P<0.01). In 10-day-old pup CBs, 1.0 microM domperidone was required to produce a significant increase of DAr (pmol/h) compared to control (P<0.005). However, control DAr (as % of total catecholamine) was about 40%; significantly higher than 24% observed in adult CBs (P<0.001). We conclude that in rabbit CB, DAr is controlled by an autoreceptor mechanism in a concentration-dependent manner and this mechanism is less developed in pups than in adults.

摘要

颈动脉体(CB)释放的多巴胺(DA)(r)被认为是由DA D2自身受体介导的反馈抑制所调节。我们测试了如下假设:CB的DA释放以浓度和年龄依赖性方式进行自身调节。使用体外CB灌注模型[Bairam, A., Marchal. F., Cottet-Emard, J.M., Basson, H., Pequignot, J.M., Hascoet, J.M., Lahiri, S., 1996b. 缺氧对发育中兔子颈动脉体多巴胺含量和释放的影响。《应用生理学杂志》80, 20 - 24。],我们在未受刺激的条件下评估了0.001、0.01、0.1、1.0和10.0微摩尔的特异性DA D2受体拮抗剂多潘立酮对成年兔子CB的DA释放的影响。对于10日龄的兔幼崽,研究了0.01、0.1、1.0微摩尔的浓度。在成年CB中,多潘立酮以浓度依赖性方式增加DA释放。与对照组(无多潘立酮)相比,从多潘立酮浓度为0.1微摩尔开始,DA释放(皮摩尔/小时)显著更高(P<0.01)。在10日龄幼崽的CB中,与对照组相比,需要1.0微摩尔的多潘立酮才能使DA释放(皮摩尔/小时)显著增加(P<0.005)。然而,对照组的DA释放(占总儿茶酚胺的百分比)约为40%;显著高于成年CB中观察到的24%(P<0.001)。我们得出结论,在兔子CB中,DA释放由自身受体机制以浓度依赖性方式控制,并且这种机制在幼崽中比在成年动物中发育程度更低。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验