Cayupe Bernardita, Morgan Carlos, Puentes Gustavo, Valladares Luis, Burgos Héctor, Castillo Amparo, Hernández Alejandro, Constandil Luis, Ríos Miguel, Sáez-Briones Patricio, Barra Rafael
Centro de Investigación Biomédica y Aplicada (CIBAP), Escuela de Medicina, Facultad de Ciencias Médicas, Universidad de Santiago de Chile (USACH), Santiago 9170020, Chile.
Laboratorio de Neurofarmacología y Comportamiento, Escuela de Medicina, Facultad de Ciencias Médicas, Universidad de Santiago de Chile, Santiago 9170020, Chile.
Molecules. 2021 Jun 11;26(12):3568. doi: 10.3390/molecules26123568.
Prenatally malnourished rats develop hypertension in adulthood, in part through increased α-adrenoceptor-mediated outflow from the paraventricular nucleus (PVN) to the sympathetic system. We studied whether both α-adrenoceptor-mediated noradrenergic excitatory pathways from the locus coeruleus (LC) to the PVN and their reciprocal excitatory CRFergic connections contribute to prenatal undernutrition-induced hypertension. For that purpose, we microinjected either α-adrenoceptor or CRH receptor agonists and/or antagonists in the PVN or the LC, respectively. We also determined the α-adrenoceptor density in whole hypothalamus and the expression levels of α-adrenoceptor mRNA in the PVN. The results showed that: (i) agonists microinjection increased systolic blood pressure and heart rate in normotensive eutrophic rats, but not in prenatally malnourished subjects; (ii) antagonists microinjection reduced hypertension and tachycardia in undernourished rats, but not in eutrophic controls; (iii) in undernourished animals, antagonist administration to one nuclei allowed the agonists recover full efficacy in the complementary nucleus, inducing hypertension and tachycardia; (iv) early undernutrition did not modify the number of α-adrenoceptor binding sites in hypothalamus, but reduced the number of cells expressing α-adrenoceptor mRNA in the PVN. These results support the hypothesis that systolic pressure and heart rate are increased by tonic reciprocal paraventricular-coerulear excitatory interactions in prenatally undernourished young-adult rats.
产前营养不良的大鼠成年后会患高血压,部分原因是α-肾上腺素能受体介导的从室旁核(PVN)到交感神经系统的传出增加。我们研究了从蓝斑(LC)到PVN的α-肾上腺素能受体介导的去甲肾上腺素能兴奋性通路及其相互的兴奋性促肾上腺皮质激素释放因子能连接是否促成了产前营养不良诱导的高血压。为此,我们分别在PVN或LC中微量注射α-肾上腺素能受体或促肾上腺皮质激素释放激素(CRH)受体激动剂和/或拮抗剂。我们还测定了整个下丘脑的α-肾上腺素能受体密度以及PVN中α-肾上腺素能受体mRNA的表达水平。结果显示:(i)激动剂微量注射可使血压正常的营养良好大鼠的收缩压和心率升高,但对产前营养不良的大鼠无效;(ii)拮抗剂微量注射可降低营养不良大鼠的高血压和心动过速,但对营养良好的对照大鼠无效;(iii)在营养不良的动物中,向一个核团给予拮抗剂可使激动剂在互补核团中恢复全部效力,从而诱发高血压和心动过速;(iv)早期营养不良并未改变下丘脑α-肾上腺素能受体结合位点的数量,但减少了PVN中表达α-肾上腺素能受体mRNA的细胞数量。这些结果支持了这样一种假说,即产前营养不良的年轻成年大鼠中,室旁核-蓝斑的兴奋性相互作用通过增强收缩压和心率来维持。