Minson J, Chalmers J, Kapoor V, Cain M, Caon A
J Hypertens. 1986 Jun;4(3):273-81. doi: 10.1097/00004872-198606000-00004.
Electrolytic lesions of the A1 noradrenaline cells in the caudal ventrolateral medulla cause transient hypertension and bradycardia in the conscious rat, as previously described in the rabbit. The lesions produced 100-fold increases in plasma arginine vasopressin, 40-fold increases in plasma adrenaline and fourfold increases in plasma noradrenaline levels. Absence of circulating vasopressin [homozygous diabetes insipidus rats (DI)] or circulating adrenaline (adrenalectomized rats) did not affect A1 hypertension, but sympathectomy with systemic 6-hydroxydopamine (6-OHDA) significantly attenuated A1 hypertension. A factorial experiment was performed to assess the relative contributions of these three peripheral effector mechanisms in a quantitative manner, with combined deficiencies of any two or of all three of these effector systems. Results suggest A1 hypertension in the rat to be primarily mediated through increased sympatho-adrenal activity. The largest component of hypertension (66%) results from increased sympathetic vasoconstrictor nerve activity, and a smaller part (34%) reflects the action of circulating adrenaline. Increases in vasopressin levels do not contribute to A1 hypertension, although vasopressin makes a major contribution to A1 lesion bradycardia.
如先前在兔身上所描述的那样,对清醒大鼠延髓尾端腹外侧的A1去甲肾上腺素能细胞进行电解损伤会导致短暂的高血压和心动过缓。这些损伤使血浆精氨酸加压素水平增加了100倍,血浆肾上腺素水平增加了40倍,血浆去甲肾上腺素水平增加了4倍。缺乏循环加压素[纯合子尿崩症大鼠(DI)]或循环肾上腺素(肾上腺切除大鼠)并不影响A1高血压,但用全身性6-羟基多巴胺(6-OHDA)进行交感神经切除术可显著减轻A1高血压。进行了一项析因实验,以定量评估这三种外周效应机制的相对贡献,即这些效应系统中任意两种或全部三种的联合缺陷。结果表明,大鼠的A1高血压主要通过交感-肾上腺活动增加介导。高血压的最大组成部分(66%)源于交感缩血管神经活动增加,较小部分(34%)反映了循环肾上腺素的作用。加压素水平升高对A1高血压没有影响,尽管加压素对A1损伤所致心动过缓起主要作用。