Department of Pharmacology, Louisiana State University Health Sciences Center and MediProfile, Inc., New Orleans, LA 70118, USA.
J Pharmacol Exp Ther. 2011 Apr;337(1):247-55. doi: 10.1124/jpet.110.175398. Epub 2011 Jan 13.
Strychnine-sensitive glycine receptors and glycine-immunoreactive fibers are expressed in the hypothalamic paraventricular nucleus (PVN), yet the functional significance of this innervation is unclear. Therefore, these studies examined the changes in cardiovascular and renal function and renal sympathetic nerve activity (RSNA) produced by the microinjection of glycine (5 and 50 nmol) into the PVN of conscious Sprague-Dawley rats. Microinjection of glycine into, but not outside of, the PVN dose-dependently increased urine flow rate and urinary sodium excretion and decreased RSNA. At the higher dose, PVN glycine also decreased heart rate; neither 5 nor 50 nmol PVN glycine altered mean arterial pressure. The glycine (50 nmol)-evoked diuresis and natriuresis were abolished in rats continuously infused intravenously with [Arg(8)]-vasopressin. Furthermore, chronic bilateral renal denervation prevented the bradycardia and diuresis to PVN glycine and blunted the natriuresis. In other studies, unilateral PVN pretreatment with the glycine receptor antagonist strychnine (1.6 nmol) prevented the effects of PVN glycine (50 nmol) on heart rate, RSNA, and renal excretory function. When microinjected bilaterally, PVN strychnine (1.6 nmol per site) evoked a significant increase in heart rate and RSNA without altering renal excretory function. These findings demonstrate that in conscious rats glycine acts in the PVN to enhance the renal excretion of water and sodium and decrease central sympathetic outflow to the heart and kidneys. Although endogenous PVN glycine inputs elicit a tonic control of heart rate and RSNA, the renal excretory responses to PVN glycine seem to be caused primarily by the inhibition of arginine vasopressin secretion.
甘氨酸敏感型的谷氨酸受体和甘氨酸免疫反应纤维存在于下丘脑室旁核(PVN)中,但这种神经支配的功能意义尚不清楚。因此,本研究检测了将甘氨酸(5 和 50nmol)微注射到清醒的 Sprague-Dawley 大鼠的 PVN 中引起的心血管和肾功能以及肾交感神经活动(RSNA)的变化。甘氨酸微注射到 PVN 中,但不在 PVN 外,可剂量依赖性地增加尿流量和尿钠排泄,并降低 RSNA。在更高的剂量下,PVN 甘氨酸也降低了心率;5nmol 和 50nmol PVN 甘氨酸均未改变平均动脉压。持续静脉内输注[Arg(8)]-加压素可消除 50nmol PVN 甘氨酸引起的利尿和排钠作用。此外,慢性双侧肾去神经支配可防止 PVN 甘氨酸引起的心动过缓和利尿,并减弱排钠作用。在其他研究中,单侧 PVN 预先用甘氨酸受体拮抗剂士的宁(1.6nmol)预处理可防止 PVN 甘氨酸(50nmol)对心率、RSNA 和肾脏排泄功能的影响。当双侧微注射时,PVN 士的宁(每个部位 1.6nmol)可引起心率和 RSNA 的显著增加,而不改变肾脏排泄功能。这些发现表明,在清醒的大鼠中,甘氨酸在 PVN 中起作用,可增强水和钠的肾脏排泄,并减少心脏和肾脏的中枢交感传出。尽管内源性 PVN 甘氨酸输入可引起心率和 RSNA 的紧张性控制,但对 PVN 甘氨酸的肾脏排泄反应似乎主要是由于抑制精氨酸加压素的分泌。