Versteeg D H, Florijn W J
Life Sci. 1987 Mar 30;40(13):1237-43. doi: 10.1016/0024-3205(87)90579-0.
The protein kinase C activator 4 beta-phorbol 12,13-dibutyrate (PDB) enhanced the electrically stimulated release of radiolabelled noradrenaline (NA), acetylcholine (ACh) and 5-hydroxytryptamine (5-HT) from dorsal hippocampal slices of the rat in vitro in a concentration-dependent manner. 4 alpha-Phorbol 12,13 didecanoate did not have an effect on the electrically stimulated release of any of the neuromessengers. Carbachol, which when present in the superfusion medium alone inhibited [14C]ACh release, significantly reduced the effect of PDB on the release of this neuromessenger. In the presence of either clonidine or [Leu5]enkephalin, which by themselves inhibited the electrically stimulated release of [3H]NA, the effect of PDB was significantly reduced. The enhancing effects of yohimbine and PDB on the electrically stimulated release of [3H]NA were additive. In all three cases, thus, the net effects of PDB were of a similar magnitude, whether the various compounds were present or not. Taken together, the present data suggest that the diacylglycerol/protein kinase C pathway is involved in the stimulus-evoked release of NA, ACh and 5-HT from dorsal hippocampal nerve terminals. Protein kinase C seems not to be involved in the modulation of the release of NA via presynaptic alpha 2-adrenoceptors and delta-opioid receptors and in that of ACh via presynaptic ACh receptors in that brain region.
蛋白激酶C激活剂4β-佛波醇12,13-二丁酸酯(PDB)以浓度依赖的方式增强了大鼠背侧海马切片在体外电刺激下放射性标记的去甲肾上腺素(NA)、乙酰胆碱(ACh)和5-羟色胺(5-HT)的释放。4α-佛波醇12,13-二癸酸酯对任何一种神经递质的电刺激释放均无影响。单独存在于灌流介质中时能抑制[14C]ACh释放的卡巴胆碱,显著降低了PDB对这种神经递质释放的作用。在可乐定或[亮氨酸5]脑啡肽单独存在时,它们自身会抑制[3H]NA的电刺激释放,此时PDB的作用显著降低。育亨宾和PDB对[3H]NA电刺激释放的增强作用是相加的。因此,在所有这三种情况下,无论是否存在各种化合物,PDB的净效应大小相似。综上所述,目前的数据表明,二酰甘油/蛋白激酶C途径参与了NA、ACh和5-HT从背侧海马神经末梢的刺激诱发释放。在该脑区,蛋白激酶C似乎不参与通过突触前α2-肾上腺素能受体和δ-阿片受体对NA释放的调节,也不参与通过突触前ACh受体对ACh释放的调节。