低盐或高盐饮食5天后幼龄达尔大鼠组织中儿茶酚胺和神经肽Y的水平。

Blood vessels Pub Date : 1991-01-01 DOI:10.1159/000158891
J Q Kong, K A Curto, W W Fleming, T A Kotchen, D A Taylor
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引用次数: 4

摘要

高盐饮食对达尔盐敏感(DS)大鼠的肠系膜血管对神经刺激和去甲肾上腺素敏感。目前的实验是为了检验对神经刺激的敏感性增强是否仅仅是由于突触后对去甲肾上腺素的超敏感性,交感神经支配的增加,递质释放的改变或另一种递质作为增强剂的存在。测定幼龄(约5周龄)雄性达尔大鼠暴露于高盐(7%)或低盐(0.45%)饮食5天后组织中儿茶酚胺含量和神经肽Y (NPY)的存在。采用电化学检测器高压液相色谱法定量测定肠系膜动脉、肾动脉、尾动脉、右心房、主动脉、输精管和肾上腺中儿茶酚胺的含量。幼龄DS大鼠和Dahl耐盐大鼠之间的品系差异(与饮食无关)仅在肾上腺素含量上可见。DS高盐(+)大鼠肠系膜动脉和右心房的去甲肾上腺素含量相对DR+降低。经壁刺激后,去甲肾上腺素从离体肠系膜血管释放到灌注液中,显示DS+和DR+制剂在基础或醋酸脱氧皮质酮(DOCA;30微米)灌注条件。在DOCA灌注中加入5微米可卡因,虽然增加了所有制剂的去甲肾上腺素总流出量,但未能区分DS+和DR+。NPY免疫荧光在DS+和DR+大鼠肠系膜动脉切片上无显著差异。因此,在检查的组织中,血管平滑肌反应性增强可能不是由高去甲肾上腺素能神经支配、NPY神经支配升高或递质释放改变来解释的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Catecholamine and neuropeptide Y levels in tissues from young Dahl rats following 5 days low- or high-salt diet.

The mesenteric vasculature of Dahl salt-sensitive (DS) rats on high-salt diet is supersensitive to nerve stimulation and to norepinephrine. The current experiments were undertaken to examine whether the enhanced sensitivity to nerve stimulation is due solely to the postsynaptic supersensitivity to norepinephrine, to increased sympathetic innervation, to altered transmitter release or to the presence of another transmitter acting as a potentiator. Catecholamine content and neuropeptide Y (NPY) presence were determined in tissues from young (approximately 5 weeks old) male Dahl rats exposed to 5 days of high (7%) or low (0.45%) salt diet. Catecholamine content from mesenteric artery, renal artery, caudal artery, right atrium, aorta, vas deferens and adrenal gland was quantified by high-pressure liquid chromatography with an electrochemical detector. A strain difference, independent of diet, between young DS and Dahl salt-resistant (DR) rats was seen only in adrenal epinephrine content. DS high-salt (+) rats displayed reduced norepinephrine content relative to DR+ in the mesenteric artery and right atrium. The release of norepinephrine from isolated mesenteric vasculature into the perfusate in response to transmural stimulation showed no significant differences between DS+ and DR+ preparations under basal, or deoxycorticosterone acetate (DOCA; 30 microM) perfusion conditions. The addition of 5 microM cocaine to the DOCA perfusion, while increasing total norepinephrine outflow in all preparations, failed to differentiate between DS+ and DR+. NPY immunofluorescence along mesenteric artery sections of DS+ and DR+ rats was not significantly different. Thus, in the tissues examined, enhanced responsiveness of vascular smooth muscle may not be explained by hypernoradrenergic innervation, elevated NPY innervation or altered release of transmitter.

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