Banasiak D, Burcher E
School of Physiology and Pharmacology, University of New South Wales, Sydney, Australia.
Peptides. 1994;15(2):333-9. doi: 10.1016/0196-9781(94)90021-3.
The autoradiographic localization of binding sites for [125I]BH-[Sar9,Met(O2)11]SP, [125I]NKA, and [125I]CGRP was investigated in adjacent sections of urinary bladder body, from adult rats pretreated 14 days before with capsaicin or vehicle. Location of silver grains was assessed both qualitatively and quantitatively using computerized densitometry. Dense labeling of smooth muscle was seen with both [125I]BH-[Sar9,Met(O2)11]SP ([125I]BHSar-SP) and [125I]NKA; in addition, [125I]BHSar-SP labeled submucosal blood vessels. For these radioligands, no differences were apparent between sections from capsaicin- and vehicle-pretreated rats. Specific binding of [125I]CGRP was observed over the epithelium and weakly over submucosal arterioles, but not over smooth muscle. The density of [125I]CGRP binding sites on the epithelium, but not blood vessels, was increased (p < 0.05) by 22% after chronic capsaicin pretreatment, suggesting receptor upregulation. This study demonstrates that although all three peptides are colocalized in primary afferent sensory fibers in rat urinary bladder, the receptors for these neuropeptides are located on different cell types and may be subject to different neural influences.
在成年大鼠膀胱体的相邻切片中,研究了[125I]BH-[Sar9,Met(O2)11]SP、[125I]NKA和[125I]CGRP结合位点的放射自显影定位,这些大鼠在14天前分别用辣椒素或赋形剂预处理。使用计算机密度测定法对银颗粒的位置进行了定性和定量评估。[125I]BH-[Sar9,Met(O2)11]SP([125I]BHSar-SP)和[125I]NKA均可见平滑肌的密集标记;此外,[125I]BHSar-SP标记了粘膜下血管。对于这些放射性配体,辣椒素预处理组和赋形剂预处理组的切片之间没有明显差异。[125I]CGRP的特异性结合在上皮细胞上观察到,在粘膜下小动脉上较弱,但在平滑肌上未观察到。慢性辣椒素预处理后,上皮细胞而非血管上的[125I]CGRP结合位点密度增加了22%(p<0.05),提示受体上调。这项研究表明,尽管这三种肽在大鼠膀胱的初级传入感觉纤维中共定位,但这些神经肽的受体位于不同的细胞类型上,并且可能受到不同的神经影响。