Barg J, Nah S Y, Levy R, Saya D, Vogel Z
Department of Neurobiology, Weizmann Institute of Science, Rehovot, Israel.
Brain Res. 1993 Nov 26;629(1):109-14. doi: 10.1016/0006-8993(93)90488-9.
beta-Endorphin, met-enkephalin and several mu-selective opioid agonists were shown to decrease thymidine incorporation into DNA in various neural cell cultures. We now report that the kappa-selective opioid agonists U50488, U69593 and MR2034 modulate [3H]thymidine incorporation into DNA in rat spinal cord-dorsal root ganglion co-cultures. U50488 at 10 microM increased by 60% thymidine incorporation in 6-day-old cultures. The thymidine incorporation induced by U50488 was blocked by the kappa-selective antagonist nor-binaltorphimine, as well as by pertussis toxin and LiCl. U50488 treatment stimulated phosphatidylinositol turnover by three-fold compared with untreated controls. These findings suggest that kappa-opioid agonists modulate DNA synthesis in spinal cord-dorsal root ganglion co-cultures through a mechanism which involves pertussis toxin-sensitive GTP-binding proteins, as well as activation of phosphatidylinositol turnover.
β-内啡肽、甲硫氨酸脑啡肽以及几种μ选择性阿片样激动剂已被证明可减少各种神经细胞培养物中胸腺嘧啶核苷掺入DNA的量。我们现在报告,κ选择性阿片样激动剂U50488、U69593和MR2034可调节大鼠脊髓-背根神经节共培养物中[3H]胸腺嘧啶核苷掺入DNA的情况。在6日龄培养物中,10微摩尔的U50488可使胸腺嘧啶核苷掺入量增加60%。U50488诱导的胸腺嘧啶核苷掺入被κ选择性拮抗剂去甲双氢吗啡酮以及百日咳毒素和氯化锂阻断。与未处理的对照相比,U50488处理使磷脂酰肌醇周转率提高了三倍。这些发现表明,κ阿片样激动剂通过一种涉及百日咳毒素敏感的GTP结合蛋白以及磷脂酰肌醇周转率激活的机制来调节脊髓-背根神经节共培养物中的DNA合成。