Ichinose Tomoko K, O'Leary Donal S, Scislo Tadeusz J
Dept. of Physiology, Wayne State Univ., School of Medicine, 540 East Canfield Ave., Detroit, MI 48201.
Am J Physiol Heart Circ Physiol. 2009 Apr;296(4):H1058-68. doi: 10.1152/ajpheart.00906.2008. Epub 2009 Feb 6.
The role of nucleus of solitary tract (NTS) A(2a) adenosine receptors in baroreflex mechanisms is controversial. Stimulation of these receptors releases glutamate within the NTS and elicits baroreflex-like decreases in mean arterial pressure (MAP), heart rate (HR), and renal sympathetic nerve activity (RSNA), whereas inhibition of these receptors attenuates HR baroreflex responses. In contrast, stimulation of NTS A(2a) adenosine receptors increases preganglionic adrenal sympathetic nerve activity (pre-ASNA), and the depressor and sympathoinhibitory responses are not markedly affected by sinoaortic denervation and blockade of NTS glutamatergic transmission. To elucidate the role of NTS A(2a) adenosine receptors in baroreflex function, we compared full baroreflex stimulus-response curves for HR, RSNA, and pre-ASNA (intravenous nitroprusside/phenylephrine) before and after bilateral NTS microinjections of selective adenosine A(2a) receptor agonist (CGS-21680; 2.0, 20 pmol/50 nl), selective A(2a) receptor antagonist (ZM-241385; 40 pmol/100 nl), and nonselective A(1) + A(2a) receptor antagonist (8-SPT; 1 nmol/100 nl) in urethane/alpha-chloralose anesthetized rats. Activation of A(2a) receptors decreased the range, upper plateau, and gain of baroreflex-response curves for RSNA, whereas these parameters all increased for pre-ASNA, consistent with direct effects of the agonist on regional sympathetic activity. However, no resetting of baroreflex-response curves along the MAP axis occurred despite the marked decreases in baseline MAP. The antagonists had no marked effects on baseline variables or baroreflex-response functions. We conclude that the activation of NTS A(2a) adenosine receptors differentially alters baroreflex control of HR, RSNA, and pre-ASNA mostly via non-baroreflex mechanism(s), and these receptors have virtually no tonic action on baroreflex control of these sympathetic outputs.
孤束核(NTS)A(2a)腺苷受体在压力反射机制中的作用存在争议。刺激这些受体可在NTS内释放谷氨酸,并引发平均动脉压(MAP)、心率(HR)和肾交感神经活动(RSNA)出现类似压力反射的降低,而抑制这些受体则会减弱HR压力反射反应。相比之下,刺激NTS A(2a)腺苷受体可增加节前肾上腺交感神经活动(pre-ASNA),并且降压和交感抑制反应不受窦主动脉去神经支配和NTS谷氨酸能传递阻断的显著影响。为了阐明NTS A(2a)腺苷受体在压力反射功能中的作用,我们比较了在氨基甲酸乙酯/α-氯醛糖麻醉的大鼠中,双侧NTS微量注射选择性腺苷A(2a)受体激动剂(CGS-21680;2.0、20 pmol/50 nl)、选择性A(2a)受体拮抗剂(ZM-241385;40 pmol/100 nl)和非选择性A(1)+ A(2a)受体拮抗剂(8-SPT;1 nmol/100 nl)前后,HR、RSNA和pre-ASNA的完整压力反射刺激-反应曲线(静脉注射硝普钠/去氧肾上腺素)。A(2a)受体的激活降低了RSNA压力反射反应曲线的范围、上平台和增益,而这些参数在pre-ASNA中均增加,这与激动剂对局部交感神经活动的直接作用一致。然而,尽管基线MAP显著降低,但沿MAP轴的压力反射反应曲线并未重置。拮抗剂对基线变量或压力反射反应功能没有显著影响。我们得出结论,NTS A(2a)腺苷受体的激活主要通过非压力反射机制差异性地改变对HR、RSNA和pre-ASNA的压力反射控制,并且这些受体对这些交感输出的压力反射控制几乎没有紧张性作用。