Gatto C, Lussky R C, Erickson L W, Berg K J, Wobken J D, Johnson D E
Department of Pediatrics, University of Minnesota, Minneapolis 55455.
J Appl Physiol (1985). 1989 Feb;66(2):573-7. doi: 10.1152/jappl.1989.66.2.573.
Calcitonin gene-related peptide (CGRP) and calcitonin (C) are two peptides that are cocontained and probably coreleased with the potent bronchocontrictors, bombesin (B) and substance P (SP), within the lung. Although CGRP and C have a wide intrapulmonary distribution, their actions have not been well defined. By the use of a computerized lung mechanics analyzer, changes in response to 10-min infusions of these agents were measured in spontaneously breathing, anesthetized guinea pigs. Infusion of 0.3 nmol.kg-1.min-1 CGRP and 2 nmol.kg-1.min-1 C caused little change in lung mechanics. Infusion of 0.06 nmol.kg-1.min-1 B and 0.3 nmol.kg-1.min-1 SP caused a marked increase in inspiratory, expiratory, and total pulmonary resistance (RT), from base-line values (P less than 0.02), with a maximal effect at 10 min postinfusion (PI) [RT = 326 +/- 20% (SE) (B), 490 +/- 73% (SP)]. Coinfusion of C or CGRP with B or SP at the above concentrations caused a marked reduction in SP - [RT = 189 +/- 28% (C), 142 +/- 16% (CGRP) at 10 min PI] and B - [RT = 157 +/- 18% (C), 158 +/- 10% (CGRP) at 10 min PI] induced changes in resistance (P less than 0.015). The mode of action of C and CGRP is unknown, but these peptides may antagonize the effects of B and SP via autonomic pathways by interfering with B- or SP-induced changes in intracellular calcium concentrations or by increasing intracellular cAMP levels by binding to specific cellular receptors linked to adenylate cyclase.
降钙素基因相关肽(CGRP)和降钙素(C)是两种与强支气管收缩剂蛙皮素(B)和P物质(SP)共同存在且可能在肺内共同释放的肽。尽管CGRP和C在肺内有广泛分布,但其作用尚未明确界定。通过使用计算机化肺力学分析仪,在自主呼吸的麻醉豚鼠中测量了对这些药物输注10分钟后的反应变化。输注0.3 nmol·kg⁻¹·min⁻¹的CGRP和2 nmol·kg⁻¹·min⁻¹的C对肺力学影响很小。输注0.06 nmol·kg⁻¹·min⁻¹的B和0.3 nmol·kg⁻¹·min⁻¹的SP可使吸气、呼气和总肺阻力(RT)从基线值显著增加(P<0.02),在输注后10分钟(PI)时达到最大效应[RT = 326±20%(SE)(B),490±73%(SP)]。上述浓度的C或CGRP与B或SP共同输注可使SP诱导的阻力变化显著降低[在PI 10分钟时,RT = 189±28%(C),142±16%(CGRP)]以及B诱导的阻力变化显著降低[在PI 10分钟时,RT = 157±18%(C),158±10%(CGRP)](P<0.015)。C和CGRP的作用方式尚不清楚,但这些肽可能通过自主神经途径拮抗B和SP的作用,即干扰B或SP诱导的细胞内钙浓度变化,或通过与连接腺苷酸环化酶的特定细胞受体结合来增加细胞内cAMP水平。