Department of Neurological Surgery, Oregon Health and Science University, Portland, Oregon 97239, USA.
J Neurosci. 2013 Jan 30;33(5):2017-28. doi: 10.1523/JNEUROSCI.4701-12.2013.
α2 adrenergic receptor (α2-AR) agonists have been used as antihypertensive agents, in the management of drug withdrawal, and as sedative analgesics. Since α2-AR agonists also influence the regulation of body temperature, we explored their potential as antipyretic agents. This study delineates the central neural substrate for the inhibition of rat brown adipose tissue (BAT) and shivering thermogenesis by α2-AR agonists. Nanoinjection of the α2-AR agonist clonidine (1.2 nmol) into the rostral raphe pallidus area (rRPa) inhibited BAT sympathetic nerve activity (SNA) and BAT thermogenesis. Subsequent nanoinjection of the α2-AR antagonist idazoxan (6 nmol) into the rRPa reversed the clonidine-evoked inhibition of BAT SNA and BAT thermogenesis. Systemic administration of the α2-AR agonists dexmedetomidine (25 μg/kg, i.v.) and clonidine (100 μg/kg, i.v.) inhibited shivering EMGs, BAT SNA, and BAT thermogenesis, effects that were reversed by nanoinjection of idazoxan (6 nmol) into the rRPa. Dexmedetomidine (100 μg/kg, i.p.) prevented and reversed lipopolysaccharide-evoked (10 μg/kg, i.p.) thermogenesis in free-behaving rats. Cholera toxin subunit b retrograde tracing from rRPa and pseudorabies virus transynaptic retrograde tracing from BAT combined with immunohistochemistry for catecholaminergic biosynthetic enzymes revealed the ventrolateral medulla as the source of catecholaminergic input to the rRPa and demonstrated that these catecholaminergic neurons are synaptically connected to BAT. Photostimulation of ventrolateral medulla neurons expressing the PRSx8-ChR2-mCherry lentiviral vector inhibited BAT SNA via activation of α2-ARs in the rRPa. These results indicate a potent inhibition of BAT and shivering thermogenesis by α2-AR activation in the rRPa, and suggest a therapeutic potential of α2-AR agonists for reducing potentially lethal elevations in body temperature during excessive fever.
α2 肾上腺素能受体 (α2-AR) 激动剂已被用作抗高血压药物、药物戒断管理和镇静镇痛药。由于 α2-AR 激动剂也影响体温调节,我们探索了它们作为解热药的潜力。本研究描绘了 α2-AR 激动剂抑制大鼠棕色脂肪组织 (BAT) 和寒战产热的中枢神经基础。将 α2-AR 激动剂可乐定 (1.2 nmol) 纳米注射到中缝苍白核区 (rRPa) 抑制 BAT 交感神经活动 (SNA) 和 BAT 产热。随后将 α2-AR 拮抗剂伊达唑兰 (6 nmol) 纳米注射到 rRPa 中,逆转了可乐定诱导的 BAT SNA 和 BAT 产热抑制。系统给予 α2-AR 激动剂右美托咪定 (25 μg/kg,iv) 和可乐定 (100 μg/kg,iv) 抑制寒战肌电图、BAT SNA 和 BAT 产热,这些作用可通过 rRPa 中伊达唑兰 (6 nmol) 的纳米注射逆转。右美托咪定 (100 μg/kg,ip) 预防和逆转了自由活动大鼠脂多糖诱导的 (10 μg/kg,ip) 产热。rRPa 中的霍乱毒素亚单位 b 逆行追踪和 BAT 中的假狂犬病毒顺行逆行追踪结合儿茶酚胺能生物合成酶免疫组化显示,腹外侧髓质是 rRPa 中儿茶酚胺能传入的来源,并表明这些儿茶酚胺能神经元与 BAT 有突触连接。表达 PRSx8-ChR2-mCherry 慢病毒载体的腹外侧髓质神经元的光刺激通过 rRPa 中 α2-AR 的激活抑制 BAT SNA。这些结果表明,rRPa 中 α2-AR 的激活对 BAT 和寒战产热具有强大的抑制作用,并表明 α2-AR 激动剂具有治疗因过度发热而导致潜在致命性体温升高的潜力。