PROLACTIN BIOACTIVITY AND THE DURATION OF LACTATIONAL AMENORRHEA

被引:15
作者
CAMPINO, C
AMPUERO, S
DIAZ, S
SERONFERRE, M
机构
[1] PONTIFICIA UNIV CATOLICA CHILE, FAC CIENCIAS BIOL, UNIDAD REPROD & DESARROLLO, SANTIAGO, CHILE
[2] PONTIFICIA UNIV CATOLICA CHILE, FAC MED, ENDOCRINOL LAB, SANTIAGO, CHILE
关键词
D O I
10.1210/jc.79.4.970
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In our population, only half of fully nursing women remain amenorrheic 6 months postpartum. The other half recover their menstrual cycles between 90-180 days postpartum in spite of a high suckling frequency and elevated immunoreactive PRL (IR-PRL) concentrations. To further investigate the association of PRL with the recovery of ovarian function, we compared PRL bioactivity (BIO-PRL) 3-4 months postpartum in fully nursing amenorrheic women who subsequently experienced long (>180 days; n = 5) or short (<180 days; n = 5) lactational amenorrhea. In the present study, BIO-PRL in plasma was measured by the Nb-2 lymphoma cell assay in samples taken before and 30 min after a suckling episode at 0800, 1600, and 2400 h. Women in the long amenorrhea group had higher overall mean BIO-PRL (mean +/- SE, 129.9 +/- 12.1 mu g/L) than nursing women in the short amenorrhea group (66.6 +/- 5.2 mu g/L; P < 0.05). Mean basal values were similar, but the women in the long amenorrhea group had more BIO-PRL in response to suckling (160.1 +/- 4.0 vs. 71.9 +/- 6.7 mu g/L; P < 0.05). Compared with their respective basal values, nursing women in the long amenorrhea group demonstrated increased BIO-PRL in response to suckling, whereas the other group did not. The relationships between BIO-PRL and IR-PRL were similar in the two groups of nursing women before suckling. However, after suckling, the long amenorrhea group had significantly higher BIO-PRL levels than IR-PRL levels (P < 0.05, by likelihood test) than the short amenorrhea group. This suggests that suckling differentially changes in each group either the composition of PRL present or substances that may modify the bioactivity of PRL in plasma.
引用
收藏
页码:970 / 974
页数:5
相关论文
共 21 条
[1]   MULTIPLE FORMS OF RAT PROLACTIN AND GROWTH-HORMONE IN PITUITARY CELL SUBPOPULATIONS SEPARATED USING A PERCOLL GRADIENT SYSTEM - DISULPHIDE-BRIDGED DIMERS AND GLYCOSYLATED VARIANTS [J].
BOLLENGIER, F ;
VELKENIERS, B ;
HOOGHEPETERS, E ;
MAHLER, A ;
VANHAELST, L .
JOURNAL OF ENDOCRINOLOGY, 1989, 120 (02) :201-&
[2]  
CAMPINO C, 1982, REV MED CHILE, V110, P139
[3]   GROWTH-HORMONE (GH) RECEPTOR ANTIBODIES WITH GH-LIKE ACTIVITY OCCUR SPONTANEOUSLY IN ACROMEGALY [J].
CAMPINO, C ;
SZECOWKA, J ;
LOPEZ, JM ;
MULCHAHEY, J ;
SERONFERRE, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1992, 74 (04) :751-756
[4]   HETEROGENEITY OF GROWTH-HORMONE PRODUCTION IN HUMAN PITUITARY-TUMOR CELLS [J].
DAVIS, JRE .
CLINICAL ENDOCRINOLOGY, 1991, 34 (01) :3-4
[5]   EARLY DIFFERENCE IN THE ENDOCRINE PROFILE OF LONG AND SHORT LACTATIONAL AMENORRHEA [J].
DIAZ, S ;
CARDENAS, H ;
BRANDEIS, A ;
MIRANDA, P ;
SCHIAPPACASSE, V ;
SALVATIERRA, AM ;
HERREROS, C ;
SERONFERRE, M ;
CROXATTO, HB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 72 (01) :196-201
[6]   CIRCADIAN VARIATION OF BASAL PLASMA PROLACTIN, PROLACTIN RESPONSE TO SUCKLING, AND LENGTH OF AMENORRHEA IN NURSING WOMEN [J].
DIAZ, S ;
SERONFERRE, M ;
CARDENAS, H ;
SCHIAPPACASSE, V ;
BRANDEIS, A ;
CROXATTO, HB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 68 (05) :946-955
[7]  
HOWIE PW, 1982, J REPROD FERTIL, V65, P545, DOI 10.1530/jrf.0.0650545
[8]   REGULATION OF AROMATASE MESSENGER-RNA AND ESTRADIOL BIOSYNTHESIS IN RAT OVARIAN GRANULOSA AND LUTEAL CELLS BY PROLACTIN [J].
KRASNOW, JS ;
HICKEY, GJ ;
RICHARDS, JS .
MOLECULAR ENDOCRINOLOGY, 1990, 4 (01) :13-21
[9]   PROLACTIN SIZE VARIANTS DURING PREGNANCY IN WOMEN WITH OVULATORY HYPERPROLACTINEMIA - CHARACTERIZATION BY ISOELECTRIC-FOCUSING AND LECTIN AFFINITY-CHROMATOGRAPHY [J].
LARREA, F ;
MENDEZ, I ;
ESCORZA, A ;
VEAYRA, F ;
CARINO, C ;
CRAVIOTO, MD .
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 1992, 44 (02) :91-100
[10]  
LIU JH, 1990, J CLIN ENDOCR METAB, V71, P605