DEVELOPMENTAL-CHANGES IN AGONIST-MEDIATED COLONIC SMOOTH-MUSCLE CONTRACTION IN THE RABBIT

被引:11
|
作者
YAGI, H
SNAPE, WJ
HYMAN, PE
机构
[1] UNIV CALIF LOS ANGELES,LOS ANGELES CTY HARBOR MED CTR,DEPT PEDIAT,1124 W CARSON ST,C-1 TRAILER,TORRANCE,CA 90509
[2] UNIV CALIF LOS ANGELES,LOS ANGELES CTY HARBOR MED CTR,DEPT MED,TORRANCE,CA 90509
[3] UNIV CALIF LOS ANGELES,LOS ANGELES CTY HARBOR MED CTR,CTR INFLAMMATORY BOWEL DIS,TORRANCE,CA 90509
关键词
D O I
10.1203/00006450-199101000-00005
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We studied smooth muscle strips from rabbit distal colon to determine age-related changes in length-tension properties and agonist-mediated contraction. Strips from newborn (1-d-old) and weanling (11-wk-old) rabbits were oriented to measure isometric tension in longitudinal muscle. Active tension comprised 47 +/- 4 and 75 +/- 5% of the total tension in the newborn and weanling, respectively. Total and active tensions in the weanling were greater than in the newborn (p < 0.001). Although the potencies for bethanechol were similar, the maximal response was nearly 9-fold greater in weanlings (6900 +/- 292 mN/cm2) versus newborns (753 +/- 112 mN/cm2), p < 0.001. Maximal stress increased with age for bethanechol, high extracellular potassium, substance P, neurokinin A, cholecystokinin octapeptide, bombesin, and serotonin. ED50 for bethanechol, substance P, neurokinin A, and bombesin did not change with age. Serotonin was 12 times more potent in newborns versus weanlings (p < 0.05). In contrast, cholecystokinin octapeptide was five times less potent in newborns (18.6 nM versus 3.4 nM, respectively, p < 0.05). Substance P-induced contractions were inhibited partially by atropine. We conclude that length-tension properties of longitudinal colonic smooth muscle differ, and responses to agonists increase with age.
引用
收藏
页码:20 / 23
页数:4
相关论文
共 50 条
  • [41] EFFECT OF ACUTE EXPERIMENTAL COLITIS ON RABBIT COLONIC SMOOTH-MUSCLE
    COHEN, JD
    KAO, HW
    TAN, ST
    LECHAGO, J
    SNAPE, WJ
    AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (04): : G538 - G545
  • [42] CONTRACTION INDUCED BY DITHIOTHREITOL IN ISOLATED RABBIT VASCULAR SMOOTH-MUSCLE
    ALLEN, JD
    CLARKE, LA
    JOURNAL OF PHYSIOLOGY-LONDON, 1979, 293 (AUG): : P77 - P78
  • [43] EXAGGERATED PROSTAGLANDIN PRODUCTION BY COLONIC SMOOTH-MUSCLE IN RABBIT COLITIS
    KAO, HW
    ZIPSER, RD
    DIGESTIVE DISEASES AND SCIENCES, 1988, 33 (06) : 697 - 704
  • [44] β-Agonist-mediated Relaxation of Airway Smooth Muscle Is Protein Kinase A-dependent
    Morgan, Sarah J.
    Deshpande, Deepak A.
    Tiegs, Brian C.
    Misior, Anna M.
    Yan, Huandong
    Hershfeld, Alena V.
    Rich, Thomas C.
    Panettieri, Reynold A.
    An, Steven S.
    Penn, Raymond B.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (33) : 23065 - 23074
  • [45] CONTRACTION OF ISOLATED SMOOTH-MUSCLE CELLS - STRUCTURAL CHANGES
    FAY, FS
    DELISE, CM
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (03) : 641 - 645
  • [46] EARLY AGONIST-MEDIATED IONIC EVENTS IN CULTURED VASCULAR SMOOTH-MUSCLE CELLS - CALCIUM MOBILIZATION IS ASSOCIATED WITH INTRACELLULAR ACIDIFICATION
    BERK, BC
    BROCK, TA
    GIMBRONE, MA
    ALEXANDER, RW
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1987, 262 (11) : 5065 - 5072
  • [47] SEROTONIN RECEPTORS IN CANINE COLONIC CIRCULAR SMOOTH-MUSCLE - INHIBITION OF CONTRACTION
    BUXTON, ILO
    ZHANG, L
    FASEB JOURNAL, 1993, 7 (03): : A27 - A27
  • [48] DEFECT IN COLONIC SMOOTH-MUSCLE CONTRACTION IN PATIENTS WITH ULCERATIVE-COLITIS
    SNAPE, WJ
    WILLIAMS, R
    HYMAN, PE
    AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (06): : G987 - G991
  • [49] MUSCARINIC RECEPTOR CONTROL OF ISOLATED COLONIC SMOOTH-MUSCLE CELL CONTRACTION
    RINGER, MJ
    KAO, HW
    HYMAN, PE
    FINN, SE
    SNAPE, WJ
    GASTROENTEROLOGY, 1986, 90 (05) : 1604 - 1604
  • [50] AGONIST-MEDIATED ACTIVATION OF PHOSPHATIDYLCHOLINE-SPECIFIC PHOSPHOLIPASE-C AND PHOSPHOLIPASE-D IN INTESTINAL SMOOTH-MUSCLE
    MURTHY, KS
    MAKHLOUF, GM
    MOLECULAR PHARMACOLOGY, 1995, 48 (02) : 293 - 304