Relaxation of porcine tracheal smooth muscle by parathyroid hormone-related protein

被引:6
|
作者
Shenberger, JS
Shew, RL
Johnson, DE
Kannan, MS
机构
[1] UNIV MINNESOTA,SCH MED,DEPT VET PATHOBIOL,MINNEAPOLIS,MN 55455
[2] UNIV MINNESOTA,SCH MED,DEPT PEDIAT,MINNEAPOLIS,MN 55455
[3] UNIV MINNESOTA,SCH MED,DEPT CELL BIOL & NEUROANAT,MINNEAPOLIS,MN 55455
[4] UNIV MINNESOTA,SCH VET MED,MINNEAPOLIS,MN 55455
来源
RESPIRATION PHYSIOLOGY | 1997年 / 107卷 / 01期
关键词
channels; K+; Ca2+-activated; mammals; pig; mediators; parathyroid hormone; muscle; smooth; airways; trachea; smooth muscle; ACTIVATED POTASSIUM CHANNELS; PTH-RELATED PROTEIN; GUINEA-PIG TRACHEA; MESSENGER-RNA; RAT; RECEPTOR; LOCALIZATION; PEPTIDE; CALCIUM; CELLS;
D O I
10.1016/S0034-5687(96)02462-0
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Parathyroid hormone-related protein (PTHrp) has been shown to relax uterine and gastrointestinal smooth muscles, but the mechanisms underlying its effects have not been characterized. Furthermore, its effect on pulmonary smooth muscle is unknown. Therefore we designed the present study to determine the PTHrp dose-response; the interaction of PTHrp and PTH; and the role of cyclic nucleotides and potassium channels in the PTHrp response in porcine tracheal smooth muscle (TSM). Our results indicate that, (1-34)PTHrp causes dose-dependent relaxation of TSM; that (1-34)PTHrp and (1-34)PTH demonstrate cross-tachyphylaxis to one another; that phosphodiesterase inhibition augments and phosphodiesterase stimulation attenuates the relaxation response while guanylate cyclase blockade has little effect, and that charybdotoxin and iberiotoxin, inhibitors of large conductance, Ca2+-activated, K+ channels, diminish the relaxation response. These findings suggest that (1-34)PTHrp-induced relaxation of TSM is mediated through a common PTHrp/PTH pathway or receptor, stimulation of cAMP and activation of large conductance, Ca2+-activated, K+ channels. (C) 1997 Elsevier Science B.V.
引用
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页码:59 / 66
页数:8
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