Bruun A, Edvinsson L, Ehinger B
Department of Ophthalmology, University Hospital, Lund, Sweden.
Acta Ophthalmol (Copenh). 1994 Jun;72(3):326-31. doi: 10.1111/j.1755-3768.1994.tb02767.x.
Neuropeptide Y is known to be present in significant amounts in the retina of most vertebrates, but its physiological actions are largely unknown. We have therefore studied its effects on the intracellular cyclic AMP accumulation in rabbit retina. Neuropeptide Y had no effect on the basal cyclic AMP level but was found to inhibit the forskolin induced cyclic AMP accumulation. There were no differences between the effects of neuropeptide Y 1-36 and neuropeptide Y 13-36 (2.4 x 10(-6) M) suggesting the presence of the Y2 subtype of neuropeptide Y receptor. D-myo-inositol-1,2,6-trisphosphate, a novel neuropeptide Y-antagonist, reduced per se the forskolin induced cyclic AMP production. The pronounced inhibitory effect of neuropeptide Y on the forskolin induced cyclic AMP production was, on the other hand, totally abolished by D-myo-inositol-1,2,6-trisphosphate. The results indicate that neuropeptide Y acts on Y2 receptors in the retina to cause an inhibition of the adenylyl cyclase activity which could be antagonized by D-myo-inositol-1,2,6-trisphosphate. Such an inhibitory action of neuropeptide Y is similar to what has been found in brain tissue, but it has not previously been reported in the retina for neuropeptide Y or any of the other retinal neuropeptides.
已知大多数脊椎动物的视网膜中都大量存在神经肽Y,但其生理作用在很大程度上尚不清楚。因此,我们研究了它对兔视网膜细胞内环磷酸腺苷(cAMP)积累的影响。神经肽Y对基础cAMP水平没有影响,但发现它能抑制毛喉素诱导的cAMP积累。神经肽Y 1-36和神经肽Y 13-36(2.4×10⁻⁶ M)的作用没有差异,这表明存在神经肽Y受体的Y2亚型。新型神经肽Y拮抗剂D-肌醇-1,2,6-三磷酸本身可降低毛喉素诱导的cAMP生成。另一方面,D-肌醇-1,2,6-三磷酸完全消除了神经肽Y对毛喉素诱导的cAMP生成的显著抑制作用。结果表明,神经肽Y作用于视网膜中的Y2受体,导致腺苷酸环化酶活性受到抑制,而D-肌醇-1,2,6-三磷酸可拮抗这种抑制作用。神经肽Y的这种抑制作用与在脑组织中发现的情况相似,但此前在视网膜中尚未有关于神经肽Y或任何其他视网膜神经肽的此类报道。