Oregon National Primate Research Center/OHSU, Beaverton, OR 97006, USA.
Am J Physiol Regul Integr Comp Physiol. 2010 Mar;298(3):R776-83. doi: 10.1152/ajpregu.00614.2009. Epub 2010 Jan 13.
Neurons in the rostral raphe pallidus (RPa) play an essential role in the regulation of sympathetically mediated metabolism and thermogenesis in brown adipose tissue (BAT). The presence of serotonergic neurons in the RPa that are retrogradely labeled following pseudorabies virus injections into BAT suggests that these neurons play a role in the regulation of BAT. In urethane/chloralose-anesthetized rats, whole body cooling decreased skin (-5.7 +/- 2.3 degrees C) and core (-1.3 +/- 0.2 degrees C) temperatures and resulted in an increase in BAT sympathetic nerve activity (SNA; +1,026 +/- 344% of baseline activity). Serial microinjections of the 5-hydroxytryptamine (5-HT) receptor antagonist, methysergide (1.2 nmol/site), but not saline vehicle, into the intermediolateral cell column (IML) in spinal segments T2-T5 markedly attenuated the cooling-evoked increase in BAT SNA (remaining area under the curve, AUC: 36 +/- 9% of naive cooling response). Microinjections of the 5-HT(1A) receptor antagonist, WAY-100635 (1.2 nmol/site), or the 5-HT(7) receptor antagonist, SB-269970 (1.2 nmol/site), into the T2-T5 IML also attenuated the cold-evoked increase in BAT SNA (remaining activity at peak inhibition: 47 +/- 8% and 39 +/- 12% of the initial cold-evoked response, respectively). The increases in BAT SNA evoked by microinjection of N-methyl-d-aspartate (NMDA) (12 pmol) or bicuculline (30 pmol) into the RPa were attenuated following microinjections of methysergide, but not saline vehicle, into the T2-T5 IML (NMDA remaining AUC, 64 +/- 13% of naive response; bicuculline remaining AUC, 52 +/- 5% of naive response). These results are consistent with our earlier demonstration of a potentiating effect of 5-HT within the IML on BAT SNA and indicate that activation of 5-HT(1A) and 5-HT(7) receptors in the spinal cord contributes to increases in BAT SNA and thermogenesis.
吻侧苍白球中的神经元在调节棕色脂肪组织(BAT)的交感神经介导的代谢和产热中起着至关重要的作用。假狂犬病毒注射到 BAT 后,逆行标记 RPa 中的 5-羟色胺能神经元表明这些神经元在 BAT 的调节中起作用。在乌拉坦/氯醛糖麻醉的大鼠中,全身降温使皮肤(-5.7 +/- 2.3°C)和核心(-1.3 +/- 0.2°C)温度降低,并导致 BAT 交感神经活动(SNA;基线活动的+1,026 +/- 344%)增加。连续微量注射 5-羟色胺(5-HT)受体拮抗剂甲麦角林(1.2 nmol/部位)而非生理盐水溶液到 T2-T5 脊髓段的中间外侧细胞柱(IML),可显著减弱冷却引起的 BAT SNA 增加(剩余曲线下面积,AUC:与基础冷却反应相比为 36 +/- 9%)。微量注射 5-HT1A 受体拮抗剂 WAY-100635(1.2 nmol/部位)或 5-HT7 受体拮抗剂 SB-269970(1.2 nmol/部位)到 T2-T5 IML 也减弱了冷诱发的 BAT SNA 增加(抑制后的剩余活性:分别为初始冷诱发反应的 47 +/- 8%和 39 +/- 12%)。微量注射 N-甲基-D-天冬氨酸(NMDA)(12 pmol)或荷包牡丹碱(30 pmol)到苍白球侧支引起的 BAT SNA 增加,在微量注射甲麦角林但不是生理盐水溶液到 T2-T5 IML 后减弱(NMDA 剩余 AUC,与基础反应相比为 64 +/- 13%;荷包牡丹碱剩余 AUC,与基础反应相比为 52 +/- 5%)。这些结果与我们之前的研究一致,即在 IML 中 5-HT 的增强作用可增强 BAT SNA,并表明脊髓中 5-HT1A 和 5-HT7 受体的激活有助于增加 BAT SNA 和产热。