Bergamaschi Cássia T, Silva Nyam F, Pires Jose G, Campos Ruy R, Neto Henrique A Futuro
Federal University of São Paulo, School of Medicine, Rua Botucatu 862, 04023-060 São Paulo, SP, Brazil.
Federal University of Espirito Santo, 29042-751 Vitória, ES, Brazil.
Int J Hypertens. 2014;2014:723939. doi: 10.1155/2014/723939. Epub 2014 Jan 21.
The hypothesis that changes in neurotransmission within the rostral ventrolateral medulla (RVLM) are important to maintain the high blood pressure (BP) was tested in Goldblatt one kidney-one clip hypertension model (1K-1C). Male Wistar rats were anesthetized (urethane 1.2 g/kg, i.v.), and the effects of bilateral microinjections into the RVLM of the following drugs were measured in 1K-1C or control groups: glutamate (0.1 mol/L, 100 nL) and its antagonist kynurenic acid (0.02 mol/L, 100 nL), the angiotensin AT1 receptor antagonist candesartan (0.01 mol/L, 100 nL), and the nonselective 5-HT receptor antagonist methiothepin (0.06 mol/L, 100 nL). Experiments in 1K-1C rats were performed 6 weeks after surgery. In anesthetized rats glutamate response was larger in hypertensive than in normotensive rats (H: Δ67 ± 6.5; N: Δ43 ± 3.54 mmHg). In contrast, kynurenic acid microinjection into the RVLM did not cause any change in BP in either group. The blockade of either AT1 or 5-HT receptors within the RVLM decreased BP only in 1K-1C rats. A largest depressor response was caused by 5-HT receptor blockade. The data suggest that 5-HT and AT1 receptors act tonically to drive RVLM in 1K-1C rats, and these actions within RVLM contribute to the pathogenesis of this model of hypertension.
在戈德布拉特单肾单夹高血压模型(1K-1C)中,对延髓头端腹外侧区(RVLM)内神经传递变化对维持高血压(BP)很重要这一假说进行了测试。雄性Wistar大鼠经麻醉(静脉注射1.2 g/kg乌拉坦),在1K-1C组或对照组中测量向RVLM双侧微量注射以下药物的效果:谷氨酸(0.1 mol/L,100 nL)及其拮抗剂犬尿喹啉酸(0.02 mol/L,100 nL)、血管紧张素AT1受体拮抗剂坎地沙坦(0.01 mol/L,100 nL)以及非选择性5-羟色胺(5-HT)受体拮抗剂甲硫噻平(0.06 mol/L,100 nL)。在手术后6周对1K-1C大鼠进行实验。在麻醉大鼠中,谷氨酸反应在高血压大鼠中比正常血压大鼠更大(H:Δ67±6.5;N:Δ43±3.54 mmHg)。相反,向RVLM微量注射犬尿喹啉酸在两组中均未引起血压任何变化。RVLM内AT1或5-HT受体的阻断仅在1K-1C大鼠中降低了血压。5-HT受体阻断引起最大的降压反应。数据表明,5-HT和AT1受体在1K-1C大鼠中持续作用以驱动RVLM,并且RVLM内的这些作用促成了该高血压模型的发病机制。