Cao Y J, Bian J T, Bhargava H N
Department of Pharmaceutics and Pharmacodynamics, The University of Illinois at Chicago, Health Sciences Center, 60612, USA.
Eur J Pharmacol. 1997 Sep 24;335(2-3):161-6. doi: 10.1016/s0014-2999(97)01216-8.
Male Swiss-Webster mice were injected intracerebroventricularly (i.c.v.) with [D-Pen2,D-Pen5]enkephalin (20 microg/mouse) twice a day for 2 days. This procedure resulted in down-regulation of binding sites for [3H][D-Pen2,D-Pen5]enkephalin as evidenced by a 52% decrease in the Bmax value. Twice daily injections of (+)-5-methyl-10,11-dihydro-5H-dibenzo-[a,d]-cyclohepten-5,10-imine (MK-801) (0.1 mg/kg, i.p.) or [(-)3-SR,4a-RS,8a-SR-6-(phosphonomethyl)-1,2,3,4,4a,5,6,7,8,8a-decahy droisoquinoline-3-carboxylic acid] (LY 235959) (2 mg/kg, i.p.), the noncompetitive and competitive antagonist of the N-methyl-D-aspartate (NMDA) receptor, respectively, for 2 days did not alter the Bmax or Kd value of [3H][D-Pen2,D-Pen5]enkephalin binding to the mouse brain. Concurrent treatment of MK-801, but not of LY 235959 with [D-Pen2,D-Pen5]enkephalin, reversed the decreases in Bmax value of [3H][D-Pen2,D-Pen5]enkephalin. Twice daily injections of [D-Ala2,Glu4] deltorphin II (20 microg/mouse) for 2 days caused an increase in the Kd value, but not the Bmax value of [3H][D-Pen2,D-Pen5]enkephalin to bind to brain membranes. Concurrent treatment of [D-Ala2,Glu4]deltorphin II with LY 235959 reversed the increase in Kd value of [3H][D-Pen2,D-Pen5]enkephalin binding induced by multiple injections of [D-Ala2,Glu4]deltorphin II, but MK-801 had no effect. The results suggest that multiple injections of delta1- and delta2-opioid receptor agonists down-regulate delta1-opioid receptors of the brain by modifying Bmax and Kd values of [3H][D-Pen2,D-Pen5]enkephalin binding, respectively. MK-801 and LY 235959 reverse delta1- and delta2-opioid receptor agonists-induced down-regulation of brain delta1-opioid receptor, respectively, apparently by different mechanisms. It is concluded that short term treatment of mice with delta1-opioid receptor agonist down-regulates brain delta1-opioid receptors by decreasing Bmax of the ligand which is partially reversed by concurrent treatment with MK-801 but not by LY 235959. On the other hand, short term treatment of mice with delta2-opioid receptor agonist down-regulates brain delta1-opioid receptors by increasing Kd of the ligand which is partially reversed by concurrent treatment with LY 235959 but not by MK-801.
雄性瑞士韦伯斯特小鼠每天经脑室内(i.c.v.)注射[D-青霉胺2,D-青霉胺5]脑啡肽(20微克/只),共注射2天。该操作导致[3H][D-青霉胺2,D-青霉胺5]脑啡肽结合位点下调,Bmax值降低52%即证明了这一点。每天两次腹腔注射(i.p.)(+)-5-甲基-10,11-二氢-5H-二苯并[a,d]环庚烯-5,10-亚胺(MK-801)(0.1毫克/千克)或[(-)3-SR,4a-RS,8a-SR-6-(膦酰甲基)-1,2,3,4,4a,5,6,7,8,8a-十氢异喹啉-3-羧酸](LY 235959)(2毫克/千克),分别作为N-甲基-D-天冬氨酸(NMDA)受体的非竞争性和竞争性拮抗剂,注射2天,并未改变[3H][D-青霉胺2,D-青霉胺5]脑啡肽与小鼠脑结合的Bmax或Kd值。MK-801与[D-青霉胺2,D-青霉胺5]脑啡肽同时给药可逆转[3H][D-青霉胺2,D-青霉胺5]脑啡肽Bmax值的降低,但LY 235959与[D-青霉胺2,D-青霉胺5]脑啡肽同时给药则无此作用。每天两次注射[D-丙氨酸2,谷氨酸4]强啡肽II(20微克/只),共注射2天,导致[3H][D-青霉胺2,D-青霉胺5]脑啡肽与脑膜结合的Kd值增加,但Bmax值未增加。LY 235959与[D-丙氨酸2,谷氨酸4]强啡肽II同时给药可逆转多次注射[D-丙氨酸2,谷氨酸4]强啡肽II诱导的[3H][D-青霉胺2,D-青霉胺5]脑啡肽结合Kd值的增加,但MK-801无此作用。结果表明,多次注射δ1和δ2阿片受体激动剂分别通过改变[3H][D-青霉胺2,D-青霉胺5]脑啡肽结合的Bmax和Kd值来下调脑内的δ1阿片受体。MK-801和LY 235959分别通过不同机制逆转δ1和δ2阿片受体激动剂诱导的脑δ1阿片受体下调。得出结论,用δ1阿片受体激动剂对小鼠进行短期治疗可通过降低配体的Bmax来下调脑δ1阿片受体,同时用MK-801治疗可部分逆转这种下调,但LY 235959则不能。另一方面,用δ2阿片受体激动剂对小鼠进行短期治疗可通过增加配体的Kd来下调脑δ1阿片受体,同时用LY 235959治疗可部分逆转这种下调,但MK-801则不能。