Bradford H F, Crowder J M, White E J
Br J Pharmacol. 1986 May;88(1):87-93. doi: 10.1111/j.1476-5381.1986.tb09474.x.
The effects of opioid agonists on veratrine-stimulated Ca2+ influx and amino acid neurotransmitter release in rat cerebrocortical brain slices were studied. Inhibitory effects were seen on both of these parameters with all of the opioid agonists used. None of the drugs used affected basal 45Ca2+ uptake, basal K+ content or basal amino acid release from the slices. At high concentrations (100 microM) fentanyl, tifluadom, U50,488H, butorphanol and bremazocine greatly inhibited the depolarization of the slices by veratrine as determined by the reduced release of K+. The opioid receptor subtypes at which the drugs were acting were characterized by the antagonistic effects of naloxone and WIN44441-3. The opioid-induced inhibition of stimulated Ca2+ uptake and amino acid release were not antagonized by WIN44441-2, the inactive enantiomer of WIN44441-3. It is concluded that opioid agonists acting through mu- and kappa-receptors and probably through delta- and sigma-receptors, have an inhibitory effect on Ca2+ uptake into cerebrocortical brain slices and the subsequent release of aspartate, glutamate and gamma-aminobutyric acid (GABA).
研究了阿片类激动剂对大鼠大脑皮质脑片中毒藜芦碱刺激的Ca2+内流和氨基酸神经递质释放的影响。在所使用的所有阿片类激动剂中,均观察到对这两个参数的抑制作用。所使用的药物均未影响脑片的基础45Ca2+摄取、基础K+含量或基础氨基酸释放。在高浓度(100 microM)时,芬太尼、替氟杜明、U50,488H、布托啡诺和布瑞马唑辛极大地抑制了由毒藜芦碱引起的脑片去极化,这是通过K+释放减少来确定的。通过纳洛酮和WIN44441-3的拮抗作用来表征药物作用的阿片受体亚型。WIN44441-3的无活性对映体WIN44441-2并未拮抗阿片类药物诱导的对刺激的Ca2+摄取和氨基酸释放的抑制作用。得出结论,通过μ和κ受体以及可能通过δ和σ受体起作用的阿片类激动剂,对Ca2+摄取到大脑皮质脑片中以及随后天冬氨酸、谷氨酸和γ-氨基丁酸(GABA)的释放具有抑制作用。