McNellis E L, Bausher L P
Department of Opthalmology and Visual Science, Yale University School of Medicine, New Haven, CT 06510.
Curr Eye Res. 1991 May;10(5):399-407. doi: 10.3109/02713689109001748.
Cyclic AMP production in response to agonists which act at a variety of receptors to either stimulate or inhibit cyclic AMP production has been studied in intact, dissected ciliary processes from rabbit eyes after unilateral surgical removal of the cervical ganglion. Cyclic AMP responses to stimulatory ligands vasoactive intestinal peptide (VIP), isoproterenol, and forskolin and inhibitory agonists neuropeptide Y (NPY), the synthetic somatostatin analogue SMS 201-995, and alpha-adrenergic agents were investigated in tissues from normal eyes and compared to the same responses in tissues from sympathetically denervated eyes. Neither stimulated cyclic AMP production nor inhibition of stimulated cyclic AMP production was significantly different in tissues from denervated vs. normal eyes. Inhibition of VIP-stimulated cyclic AMP production by epinephrine and paraaminoclonidine in tissues from both normal and denervated eyes was blocked by the alpha 2-adrenergic antagonist yohimbine but not by the alpha 1-adrenergic antagonist prazosin. These data indicate that the VIP, NPY, somatostatin, and alpha 2- and beta 2-adrenergic receptors which regulate cyclic AMP production in rabbit ciliary processes are postjunctional and suggest that ligands known to modulate cyclic AMP levels in this tissue may exert effects on aqueous humor formation independently of adrenergic innervation.
在单侧手术切除颈神经节后,对兔眼完整的、解剖的睫状体中,针对作用于多种受体以刺激或抑制环磷酸腺苷(cAMP)生成的激动剂所引发的cAMP生成情况进行了研究。研究了正常眼组织和去交感神经眼组织中环磷酸腺苷对刺激性配体血管活性肠肽(VIP)、异丙肾上腺素和福斯可林以及抑制性激动剂神经肽Y(NPY)、合成生长抑素类似物SMS 201-995和α-肾上腺素能药物的反应,并将其与去交感神经眼组织中的相同反应进行比较。去神经眼组织与正常眼组织相比,无论是刺激cAMP生成还是抑制刺激的cAMP生成,均无显著差异。正常眼和去神经眼组织中,肾上腺素和对氨基可乐定对VIP刺激的cAMP生成的抑制作用,被α2-肾上腺素能拮抗剂育亨宾阻断,但未被α1-肾上腺素能拮抗剂哌唑嗪阻断。这些数据表明,在兔睫状体中调节cAMP生成的VIP、NPY、生长抑素以及α2和β2-肾上腺素能受体是节后受体,并提示已知调节该组织中环磷酸腺苷水平的配体可能独立于肾上腺素能神经支配对房水生成产生影响。