Ortega-Alvaro A, Chover-Gonzalez A J, Lai-Kuen R, Mico J A, Gibert-Rahola J, Fournié-Zaluski M C, Roques B P, Maldonado R
Département de Pharmacochimie Moléculaire et Structurale, U266 INSERM, URA D1500 CNRS, UFR des Sciences Pharmaceutiques et Biologiques 4, Paris, France.
Eur J Pharmacol. 1998 Sep 4;356(2-3):139-48. doi: 10.1016/s0014-2999(98)00525-1.
This study was undertaken to investigate the effects induced by the systemic administration of RB 101 [N-[(R,S)-2-benzyl-3[(S)(2-amino-4-methylthio)butyl dithio]-1-oxoprpyl]-L-phenylalanine benzyl ester], a mixed inhibitor of the enkephalin catabolism able to cross the blood-brain barrier, in antinociception produced by adrenal medullary tissue transplanted in the rat spinal subarachnoid space. For this purpose, the antinociceptive responses induced by intravenous (i.v.) administration of RB 101 were evaluated in the tail-flick in rats transplanted 28 and 56 days before the test. Systemic administration of RB 101 induced antinociceptive effects in sham-operated rats, as previously reported. RB 101 also enhanced significantly the antinociception produced by the autotransplant 28 and 56 days after surgery. The antinociceptive responses of RB 101 in both sham-operated and autotransplanted rats were blocked by naloxone, but were not modified by the noradrenergic antagonist, phentolamine, suggesting a selective involvement of opioid mechanisms. The present results indicate that the inhibitors of enkephalin catabolism enhance the antinociception induced by adrenal medullary transplants.
本研究旨在探讨全身给予RB 101 [N-[(R,S)-2-苄基-3[(S)(2-氨基-4-甲硫基)丁基二硫代]-1-氧代丙基]-L-苯丙氨酸苄酯](一种能够穿过血脑屏障的脑啡肽分解代谢混合抑制剂)对大鼠脊髓蛛网膜下腔移植肾上腺髓质组织产生的抗伤害感受的影响。为此,在试验前28天和56天进行移植的大鼠中,评估静脉注射(i.v.)RB 101诱导的抗伤害感受反应。如先前报道,全身给予RB 101在假手术大鼠中诱导了抗伤害感受作用。RB 101还显著增强了术后28天和56天自体移植产生的抗伤害感受。纳洛酮阻断了RB 101在假手术和自体移植大鼠中的抗伤害感受反应,但去甲肾上腺素能拮抗剂酚妥拉明对其无影响,提示阿片类机制的选择性参与。目前的结果表明,脑啡肽分解代谢抑制剂增强了肾上腺髓质移植诱导的抗伤害感受。