Katovich M J, Aerni J D, Cespedes A T, Rowland N E
Department of Pharmacodynamics, University of Florida, Gainesville, FL 32610, USA.
Physiol Behav. 2001 Mar;72(4):621-7. doi: 10.1016/s0031-9384(01)00415-2.
We have shown previously that administration of angiotensin II (Ang II) produces an apparent decrease in thermoregulatory set point. Exposure to high salt diets either perinatally or later in life has been shown to increase pressor responsiveness to administration of Ang II, so in the present studies we examine whether high dietary NaCl would also increase the thermal responsiveness to Ang II. In the first study, we show that exposure to a basal NaCl diet (0.12%) during gestation through 4 weeks postnatally produced very large elevations in plasma renin activity (PRA) and aldosterone concentrations in the offspring. Exposure to high salt diet (3%) did not decrease the levels of these parameters below those fed mid salt diet (1%). In the second study, we show that rats raised through 4 weeks of age on basal diet, but then fed standard chow until adulthood, showed greater changes in tail skin (T(sk)) and colonic (T(c)) temperatures following administration of Ang II (200 microg/kg sc) than either mid- or high-salt-raised groups. In the third study, we confirmed this finding and extended it to show that rats raised on a very high salt diet (6%) also did not differ from the mid-salt group. In both studies, acute water intake measured in a separate test following administration of Ang II did not differ as a function of perinatal salt diet. In a fourth study, the period of exposure to the diets was extended from the perinatal period through adulthood and, surprisingly, there was no longer an enhanced thermal response to Ang II in basal diet rats compared with rats fed the very high salt diet. In the final study, rats raised on a regular diet but exposed only as adults to the test diets showed a nonsignificant trend toward a decreased thermal response in the basal group. Thus, dietary salt level may have opposite effects on Ang II effects on adult thermoregulation, depending on the age at the exposure.
我们之前已经表明,给予血管紧张素II(Ang II)会使体温调节设定点明显降低。研究表明,围产期或生命后期摄入高盐饮食会增加对给予Ang II的升压反应性,因此在本研究中,我们研究高盐饮食是否也会增加对Ang II的热反应性。在第一项研究中,我们表明,从妊娠期到出生后4周暴露于基础NaCl饮食(0.12%)会使后代的血浆肾素活性(PRA)和醛固酮浓度大幅升高。暴露于高盐饮食(3%)并没有使这些参数水平低于摄入中盐饮食(1%)的水平。在第二项研究中,我们表明,在基础饮食中饲养至4周龄,但随后喂食标准食物直至成年的大鼠,给予Ang II(200微克/千克皮下注射)后,尾皮肤温度(T(sk))和结肠温度(T(c))的变化比中盐或高盐饲养组更大。在第三项研究中,我们证实了这一发现,并进一步表明,以非常高的盐饮食(6%)饲养的大鼠与中盐组也没有差异。在这两项研究中,给予Ang II后在单独测试中测量的急性饮水量并没有因围产期盐饮食而有所不同。在第四项研究中,饮食暴露期从围产期延长至成年期,令人惊讶的是,与喂食非常高盐饮食的大鼠相比,基础饮食大鼠对Ang II的热反应不再增强。在最后一项研究中,以常规饮食饲养但仅在成年期暴露于测试饮食的大鼠,基础组的热反应有降低的趋势,但不显著。因此,饮食盐水平对Ang II对成年体温调节的影响可能有相反的作用,这取决于暴露时的年龄。