Matherne G P, Nakamura K T, Robillard J E
Department of Pediatrics, University of Iowa College of Medicine, Iowa City 52242.
Am J Physiol. 1988 Feb;254(2 Pt 2):R277-83. doi: 10.1152/ajpregu.1988.254.2.R277.
The renal hemodynamic response to renal arterial infusions of guanabenz (alpha 2-adrenoceptor agonist) and phenylephrine (alpha 1-adrenoceptor agonist) were compared in conscious and chronically instrumented fetal (132-140 days gestation; term 145 days), newborn (6-15 days postnatal), and nonpregnant adult sheep. Phenylephrine produced similar dose-related decreases in renal blood flow velocity in all three groups at low concentrations (less than 1.8 X 10(-7) M) of drug in renal blood, whereas at the highest concentration adults demonstrated the most vasoconstriction and newborns the least (P less than 0.05 ANOVA). Responses to phenylephrine infusion during renal alpha 1-adrenoceptor blockade with prazosin were completely inhibited. Guanabenz produced greater renal vasoconstriction in adult sheep (P less than 0.05 ANOVA) at all concentrations (0.6 X 10(-6) to 8 X 10(-6) M) when compared with fetal and newborn sheep. Guanabenz-mediated vasoconstriction was not affected by alpha 1-adrenoceptor blockade with prazosin but was completely inhibited by the addition of an alpha 2-adrenoceptor antagonist idazoxan. Results of the present study demonstrate that renal vasoconstriction is mediated by both alpha 1- and alpha 2-adrenoceptors in fetal, newborn, and adult sheep. Moreover, these results suggest that renal alpha 1- and alpha 2-adrenoceptor-mediated vasoconstrictor responses mature at different rates.
在清醒且长期植入仪器的胎羊(妊娠132 - 140天;足月为145天)、新生羊(出生后6 - 15天)和未孕成年羊中,比较了肾动脉输注胍那苄(α₂ - 肾上腺素能受体激动剂)和去氧肾上腺素(α₁ - 肾上腺素能受体激动剂)时的肾血流动力学反应。在肾血中低浓度(小于1.8×10⁻⁷M)药物时,去氧肾上腺素在所有三组中均产生了类似的剂量相关的肾血流速度降低,而在最高浓度时,成年羊表现出最强的血管收缩,新生羊最弱(方差分析,P < 0.05)。在用哌唑嗪进行肾α₁ - 肾上腺素能受体阻滞期间,对去氧肾上腺素输注的反应被完全抑制。与胎羊和新生羊相比,在所有浓度(0.6×10⁻⁶至8×10⁻⁶M)下,胍那苄在成年羊中产生了更强的肾血管收缩(方差分析,P < 0.05)。胍那苄介导的血管收缩不受哌唑嗪对α₁ - 肾上腺素能受体阻滞的影响,但加入α₂ - 肾上腺素能受体拮抗剂咪唑克生后被完全抑制。本研究结果表明,在胎羊、新生羊和成年羊中,肾血管收缩由α₁ - 和α₂ - 肾上腺素能受体介导。此外,这些结果表明肾α₁ - 和α₂ - 肾上腺素能受体介导的血管收缩反应以不同速率成熟。