The effect of oxytocin antagonist on uterus in response to exogenous oxytocin

被引:3
作者
Park, SH
Song, CH
Pak, SC
Flouret, G
Wilson, L
机构
[1] Dongshin Univ, Oriental Med Sch, Naju 520714, South Korea
[2] Chosun Univ, Sch Med, Dept Obstet & Gynecol, Kwangju 501759, South Korea
[3] Northwestern Univ, Sch Med, Dept Physiol, Chicago, IL 60611 USA
[4] Univ Illinois, Dept Obstet & Gynecol, Chicago, IL 60612 USA
关键词
oxytocin; oxytocin antagonist; uterus; receptor; labor;
D O I
10.3346/jkms.2000.15.3.299
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study was performed to determine the action mode of oxytocin antagonist, In Study 1, the duration of in vivo action of oxytocin antagonist I (AI) was examined, After infusing AI, oxytocin was given and repeated every hour for 5 hr. Uterine activities were monitored with a polygraph, Study 2 determined the effect of AI on uterine oxytocin receptor number (Rn) and binding affinity (Kd). AI treated rats were sacrificed at 0.5 and 4 hr later for receptor assay, In Study 1, the uterine contractile response to oxytocin was significantly inhibited (p<0.05) compared to controls at five min, 1 and 2 hr after injection of AI. No differences in response were detected compared to controls (p<0.05) at later hours. In Study 2, no differences (p>0.05) between the AI and control animals in either oxytocin receptor number or binding affinity was found. These data suggest that the major mode of AI action is via competitive inhibition at the uterine oxytocin receptor and not by altering receptor number or binding affinity. AI is suggested to have the potential of being a potent and specific tocolytic agent for prevention of preterm labor in human.
引用
收藏
页码:299 / 302
页数:4
相关论文
共 16 条
[1]   INHIBITION OF UTERINE CONTRACTIONS OF PREMATURE LABOR WITH AN OXYTOCIN ANALOG - RESULTS FROM A PILOT-STUDY [J].
AKERLUND, M ;
STROMBERG, P ;
HAUKSSON, A ;
ANDERSEN, LF ;
LYNDRUP, J ;
TROJNAR, J ;
MELIN, P .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1987, 94 (11) :1040-1044
[2]   OXYTOCIN RECEPTOR BLOCKADE - A NEW PRINCIPLE IN THE TREATMENT OF PRETERM LABOR [J].
ANDERSEN, LF ;
LYNDRUP, J ;
AKERLUND, M ;
MELIN, P .
AMERICAN JOURNAL OF PERINATOLOGY, 1989, 6 (02) :196-199
[3]   Comparison of the in vivo activity of different oxytocin antagonists in the pregnant baboon [J].
Fejgin, MD ;
Pak, SC ;
Flouret, G ;
Parsons, MT ;
Wilson, L .
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 1998, 5 (05) :251-254
[4]  
Fuchs A. R, 1970, Biology Reprod., V2, P387, DOI 10.1095/biolreprod2.3.387
[5]   CORRELATION BETWEEN OXYTOCIN RECEPTOR CONCENTRATION AND RESPONSIVENESS TO OXYTOCIN IN PREGNANT RAT MYOMETRIUM - EFFECTS OF OVARIAN-STEROIDS [J].
FUCHS, AR ;
PERIYASAMY, S ;
ALEXANDROVA, M ;
SOLOFF, MS .
ENDOCRINOLOGY, 1983, 113 (02) :742-749
[6]   THE EFFECT OF THE OXYTOCIN ANTAGONIST ATOSIBAN ON PRETERM UTERINE ACTIVITY IN THE HUMAN [J].
GOODWIN, TM ;
PAUL, R ;
SILVER, H ;
SPELLACY, W ;
PARSONS, M ;
CHEZ, R ;
HAYASHI, R ;
VALENZUELA, G ;
CREASY, GW ;
MERRIMAN, R .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1994, 170 (02) :474-478
[7]   EVALUATION OF 1-DEAMINO-[D-TYR(OETHYL)2,THR4,ORN8] VASOTOCIN, AN OXYTOCIN ANTAGONIST, IN ANIMAL-MODELS OF UTERINE CONTRACTILITY AND PRETERM LABOR - A NEW TOCOLYTIC AGENT [J].
HAHN, DW ;
DEMAREST, KT ;
ERICSON, E ;
HOMM, RE ;
CAPETOLA, RJ ;
MCGUIRE, JL .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1987, 157 (04) :977-982
[8]   DO TOCOLYTIC AGENTS STOP PRETERM LABOR - A CRITICAL AND COMPREHENSIVE REVIEW OF EFFICACY AND SAFETY [J].
HIGBY, K ;
XENAKIS, EMJ ;
PAUERSTEIN, CJ ;
HARBERT, GM ;
JONES, H ;
MERKATZ, IR ;
CREASY ;
WOODS, J ;
CEFALO, RC ;
GIBBS, RS ;
SCOTT, S ;
QUEENAN, JT ;
KIRSCHBAUM ;
NELSON, K .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1993, 168 (04) :1247-1259
[9]   OXYTOCIN GENE-EXPRESSION IN RAT UTERUS [J].
LEFEBVRE, DL ;
GIAID, A ;
BENNETT, H ;
LARIVIERE, R ;
ZINGG, HH .
SCIENCE, 1992, 256 (5063) :1553-1555
[10]   ANALYSIS OF RADIOLIGAND BINDING EXPERIMENTS - A COLLECTION OF COMPUTER-PROGRAMS FOR THE IBM-PC [J].
MCPHERSON, GA .
JOURNAL OF PHARMACOLOGICAL METHODS, 1985, 14 (03) :213-228