Lin M T, Chern Y F, Wang Z, Wang H S
Can J Physiol Pharmacol. 1979 May;57(5):469-75. doi: 10.1139/y79-071.
Either systemic or central administration of apomorphine produced dose-related decreases in rectal temperature at ambient temperatures (Ta) of 8 and 22 degrees C in rats. At Ta = 8 degrees C, the hypothermia was brought about by a decrease in metabolic rate (M). At Ta = 22 degrees C, the hypothermia was due to an increase in mean skin temperature, an increase in respiratory evaporative heat loss (Eres) and a decrease in M. This increased mean skin temperature was due to increased tail and foot skin temperatures. However, at Ta = 29 degrees C, apomorphine produced increased rectal temperatures due to increased M and decreased Eres. Moreover, the apomorphine-induced hypothermia or hyperthermia was antagonized by either haloperidol or 6-hydroxydopamine, but not by 5,6-dihydroxytryptamine. The data indicate that apomorphine acts on dopamine neurons within brain, with both pre- and post-synaptic sites of action, to influence body temperature.
在大鼠中,无论是全身给药还是中枢给药,阿扑吗啡在8℃和22℃的环境温度(Ta)下均会导致直肠温度呈剂量依赖性下降。在Ta = 8℃时,体温过低是由代谢率(M)降低引起的。在Ta = 22℃时,体温过低是由于平均皮肤温度升高、呼吸蒸发散热(Eres)增加和M降低。这种平均皮肤温度升高是由于尾巴和足部皮肤温度升高所致。然而,在Ta = 29℃时,阿扑吗啡由于M增加和Eres降低而导致直肠温度升高。此外,阿扑吗啡诱导的体温过低或体温过高可被氟哌啶醇或6-羟基多巴胺拮抗,但不能被5,6-二羟基色胺拮抗。数据表明,阿扑吗啡作用于脑内的多巴胺神经元,作用于突触前和突触后位点,以影响体温。