Crofton J T, Ota M, Share L
Department of Physiology and Biophysics, University of Tennessee, Memphis 38163.
J Hypertens. 1993 Oct;11(10):1031-8. doi: 10.1097/00004872-199310000-00005.
To determine the roles of vasopressin, the renin-angiotensin system and sex in the pathogenesis of salt-sensitive hypertension in the Dahl rat.
The effects of 12 days' treatment with a non-peptide, orally effective V1 antagonist (OPC-21,268) and captopril, individually or together, were compared in male and female Dahl salt-sensitive rats after 10 days on a high-salt diet.
OPC-21,268 was given in the food, and captopril was administered with osmotic pumps implanted subcutaneously.
Systolic blood pressure (SBP) reached a higher level in untreated males than in untreated females. V1 blockade in males prevented any further increase in SBP during the first week of treatment, but SBP rose thereafter towards the levels found in the untreated males. In females OPC-21,268 had no effect. In males captopril prevented any further increase in SBP. There was no effect of captopril in females during the first week of treatment, but SBP fell to pretreatment levels during the second week. Combined treatment with OPC-21,268 and captopril in males had a smaller antihypertensive effect than either drug alone. In females combined treatment prevented any further increase in SBP.
These findings suggest that both vasopressin and the renin-angiotensin system contribute to the pathogenesis of Dahl salt-sensitive hypertension, but that other factors, possibly including the sympathetic nervous system, are also involved. Sex also affects the severity of this form of hypertension and influences the relative roles of vasopressin and the renin-angiotensin system. It is likely that the gonadal steroid hormones modulate the activity of the pathogenetic factors in this form of hypertension at a central or peripheral level.
确定血管加压素、肾素 - 血管紧张素系统及性别在Dahl大鼠盐敏感性高血压发病机制中的作用。
在高盐饮食10天后,对雄性和雌性Dahl盐敏感性大鼠单独或联合给予非肽类口服有效的V1拮抗剂(OPC - 21,268)和卡托普利进行12天治疗,比较其效果。
OPC - 21,268混入食物中给予,卡托普利通过皮下植入渗透泵给药。
未治疗的雄性大鼠收缩压(SBP)达到的水平高于未治疗的雌性大鼠。雄性大鼠V1受体阻断在治疗的第一周阻止了SBP的进一步升高,但此后SBP上升至未治疗雄性大鼠的水平。在雌性大鼠中,OPC - 21,268无作用。在雄性大鼠中,卡托普利阻止了SBP的进一步升高。在治疗的第一周,卡托普利对雌性大鼠无作用,但在第二周SBP降至治疗前水平。雄性大鼠联合使用OPC - 21,268和卡托普利的降压效果小于单独使用任一药物。在雌性大鼠中,联合治疗阻止了SBP的进一步升高。
这些发现表明,血管加压素和肾素 - 血管紧张素系统均参与Dahl盐敏感性高血压的发病机制,但其他因素(可能包括交感神经系统)也与之相关。性别也影响这种高血压形式的严重程度,并影响血管加压素和肾素 - 血管紧张素系统的相对作用。性腺甾体激素可能在中枢或外周水平调节这种高血压形式中致病因素的活性。