Berner N J, Grahn D A, Heller H C
Department of Biological Sciences, Stanford University, Stanford, CA 94305-5020, USA.
Brain Res. 1999 Jun 12;831(1-2):155-64. doi: 10.1016/s0006-8993(99)01426-2.
The nucleus raphe magnus (NRM) is purported to be a relay through which peripheral thermoafferent information is transmitted to thermointegrative centers located in the preoptic/anterior hypothalamus (POAH). Therefore, suppression of neural activity in the NRM should reduce thermoregulatory responses to peripheral thermal challenges, but not affect responses elicited by manipulation of POAH temperature. At low ambient temperatures lidocaine injections into the NRM of nonanesthetized rats resulted in decreases in POAH temperature, oxygen consumption, and electromyographic activity. At a warm ambient temperature, lidocaine injections into the NRM decreased the elevations in oxygen consumption and electromyographic activity elicited by cooling the POAH. The effects of lidocaine injections were duplicated by injection of a 5-HT(1A) agonist 8-hydroxy-dipropylaminotetralin (8-OH-DPAT) into the NRM. The effect of 8-OH-DPAT was eliminated by pre-treatment with a selective autoreceptor antagonist. These results suggest that NRM 5-HT neurons are modulating the relationship between output of thermointegrative centers and thermoregulatory effector responses rather than processing thermoafferent information.
中缝大核(NRM)被认为是一个中继站,外周热传入信息通过它被传递到位于视前区/下丘脑前部(POAH)的体温整合中枢。因此,抑制NRM中的神经活动应会减少对外周热刺激的体温调节反应,但不会影响由POAH温度操控所引发的反应。在低环境温度下,向未麻醉大鼠的NRM注射利多卡因会导致POAH温度、耗氧量和肌电图活动降低。在温暖的环境温度下,向NRM注射利多卡因会降低因冷却POAH所引发的耗氧量和肌电图活动的升高。向NRM注射5-羟色胺(1A)激动剂8-羟基-二丙基氨基四氢萘(8-OH-DPAT)可重现利多卡因注射的效果。8-OH-DPAT的作用可通过用选择性自身受体拮抗剂预处理来消除。这些结果表明,NRM 5-羟色胺能神经元正在调节体温整合中枢的输出与体温调节效应器反应之间的关系,而不是处理热传入信息。