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Neuroendocrine peptides neuropeptide‐Y (NPY) and peptide‐YY (PYY) suppress Cl secretion and K secretion in guinea pig distal colon through action at Y2‐receptors

机译:神经内分泌肽神经肽-Y(NPY)和肽-YY(PYY)抑制在豚鼠远端结肠中的Cl分泌和K分泌通过Y2-受体的作用

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摘要

Electrogenic Cl– and K+ secretion in isolated mucosa from guinea pig distal colon measured as short-circuit current (Isc) and transepithelial conductance (Gt) were stimulated by epinephrine (epi), prostaglandin-E2 (PGE2) and carbachol (CCh). neuropeptide-Y (NPY) and peptide-YY (PYY) inhibited by 60% Cl– secretion activated by either PGE2 or PGE2+CCh with EC50’s of 16nM and 6nM, respectively. Neither peptide markedly inhibited the transient component of the PGE2+CCh response. Immunoreactivity (IR) for NPY was present in enteric ganglia and in proximity with crypts. Basolateral membranes of colonic crypt and surface epithelial cells had distinct IR for neuropeptide-Y receptors Y1 and Y2. Receptor expression was supported further by immuno-blot showing bands at molecular weights consistent with monomer and oligomer. Sub-type selective antagonists BVD10 (Y1) and BIIE0246 (Y2) indicated that secretory suppression occurred through Y2 receptors. The Y2 selective peptide PYY(3-36) also suppressed Cl– secretion with a EC50 of 9nM. BIIE0246 addition increased Isc and Gt during PGE2 or PGE2+CCh activation consistent with the presence of in vitro released PYY or NPY. PYY addition increased the epi EC50 to 18nM compared with BIIE0246 treated tissues, 4nM. Thus, PYY or NPY suppressed Cl– secretory capacity and desensitized the adrenergic K+ secretory response, providing a negative feedback for secretory activation. [supported by NIH, DK65845]
机译:通过肾上腺素(EPI),前列腺素-E2(PGE2)和卡酰基(CCH)刺激从豚鼠远端结肠中测量的豚鼠远端结肠中的豚鼠远端结肠中的隔离粘膜中的电力Cl-和K +分泌物。神经肽-Y(NPY)和肽-YY(PYY)抑制了通过PGE2或PGE2 + CCH活化的60%Cl-分泌,分别具有12nm和6nm的EC50和6nm。肽均明显抑制PGE2 + CCH响应的瞬态分量。 NPY的免疫反应性(IR)存在于肠道神经节,并与隐窝接近。结肠隐窝和表面上皮细胞的基石外侧膜对神经肽-Y受体Y1和Y2具有不同的IR。通过与单体和低聚物一致的分子量的免疫印迹进一步支持受体表达。亚型选择性拮抗剂BVD10(Y1)和BIE0246(Y2)表明,通过Y2受体发生分泌抑制。 Y2选择性肽PYY(3-36)也抑制了9nm的EC50的CL-分泌。 Bie0246在PGE2或PGE2 + CCH激活期间添加增加的ISC和GT,这与体外释放的PYY或NPY的存在一致。 PYY添加了与BIE0246治疗组织,4nm的EPI EC50至18nm。因此,PYY或NPY抑制了CL-分泌能力并脱敏的肾上腺素能K +分泌响应,为分泌激活提供负反馈。 [由NIH,DK65845支持]

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