Cohn M L, Cohn M, Taylor P H
Science. 1978 Jan 20;199(4326):319-22. doi: 10.1126/science.202029.
The dibutyryl derivative of guanosine 3',5'-monophosphate (cyclic GMP), administered centrally, totally abolishes response to noxious stimuli without depressing the central nervous system. Analgesic properties of the nucleotide are not reversed by naloxone. Microinjected intracerebrally into different sites, dibutyryl cyclic GMP does not mimic the action of morphine. Pharmacological effects of dibutyryl cyclic GMP suggest that endogenous cyclic GMP modulates an inhibitory pain pathway distinct from that on which morphine acts.
3',5'-环磷酸鸟苷(环磷鸟苷)的二丁酰衍生物经中枢给药后,可完全消除对伤害性刺激的反应,而不抑制中枢神经系统。纳洛酮不能逆转该核苷酸的镇痛特性。将二丁酰环磷鸟苷微量注射到脑内不同部位,它并不模拟吗啡的作用。二丁酰环磷鸟苷的药理作用表明,内源性环磷鸟苷调节的是一条不同于吗啡作用的抑制性疼痛通路。