Zagon I S, McLaughlin P J
Neurobehav Toxicol Teratol. 1984 Jul-Aug;6(4):319-23.
Adult rats maternally exposed to methadone during gestation and/or lactation were tested for thermogenic responsiveness and nociceptive thresholds following acute injections of various drugs. Hot-plate latencies were recorded initially and at 1 hr following amphetamine, chloropromazine, cocaine, diazepam, ethanol or morphine administration. Rectal temperatures were recorded initially and 1, 3 and 5 hr after administration of each of these drugs. Perinatal exposure to methadone resulted in tolerance to the thermoregulatory actions of chlorpromazine and amphetamine in at least one sex of each treatment group. However, sensitivity to thermogenic response was recorded following morphine administration in rats exposed to methadone only in utero or during both gestation and lactation. An enhanced sensitivity to nociceptive thresholds was recorded in methadone-treated rats after amphetamine, cocaine and morphine injections. These results, in concert with earlier findings of altered response to methadone challenge, suggest that perinatal exposure to methadone produces specific long-term effects on the neural mechanisms underlying thermoregulation and nociception.
对在妊娠和/或哺乳期母体内接触过美沙酮的成年大鼠,在急性注射各种药物后测试其产热反应性和痛觉阈值。最初以及在注射苯丙胺、氯丙嗪、可卡因、地西泮、乙醇或吗啡1小时后记录热板潜伏期。在注射每种药物后最初以及1、3和5小时记录直肠温度。围产期接触美沙酮导致每个治疗组至少一种性别的大鼠对氯丙嗪和苯丙胺的体温调节作用产生耐受性。然而,仅在子宫内或在妊娠和哺乳期均接触美沙酮的大鼠在注射吗啡后记录到产热反应敏感性。在注射苯丙胺、可卡因和吗啡后,美沙酮治疗的大鼠对痛觉阈值的敏感性增强。这些结果,连同早期关于对美沙酮激发反应改变的发现,表明围产期接触美沙酮会对体温调节和痛觉的神经机制产生特定的长期影响。