CIRCADIAN PROFILE OF PLASMA CALCITONIN GENE-RELATED PEPTIDE IN HEALTHY MAN

被引:50
作者
TRASFORINI, G
MARGUTTI, A
PORTALUPPI, F
MENEGATTI, M
AMBROSIO, MR
BAGNI, B
PANSINI, R
UBERTI, ECD
机构
[1] UNIV FERRARA, INST INTERNAL MED, ENDOCRINOL SECT, VIA SAVONAROLA 9, I-44100 FERRARA, ITALY
[2] ST ANNA HOSP, DEPT NUCL MED, I-44100 FERRARA, ITALY
关键词
D O I
10.1210/jcem-73-5-945
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Calcitonin gene-related peptide (CGRP) is known to exert potent cardiovascular effects and is presumed to participate in the neural control of circulation and blood flow. It has been assayed in many physiological and disease conditions, yet virtually nothing is known of the normal fluctuations in its circulating levels. We have studied the variability throughout a 24-h period of plasma concentrations of CGRP in eight recumbent healthy volunteers (four men and four women, 25-37 yr old), after careful standardization of their daily diet and routine schedules. A correlation with the circadian rhythms of blood pressure (BP), heart rate (HR), and plasma aldosterone (PA), PRA, plasma cortisol (PC), and atrial natriuretic peptide (ANP) was also made. Plasma CGRP concentrations ranged from a mean peak value of 18.1 +/- 1.5 pmol/L to a mean lowest value of 11.7 +/- 0.4 pmol/L (P < 0.05). The mean circadian acrophase of CGRP (calculated by cosinor analysis to occur at 2314 h) anticipated the corresponding acrophases of the other hormones (0122, 0528, 0809, and 0840 h for ANP, PRA, PA, and PC, respectively). Instead, BP and HR rhythms seemed to be antiphasic with the ANP rhythm (calculated acrophases occurred at 1356, 1339, and 1314 h for systolic BP, diastolic BP, and HR, respectively). Our data demonstrate that, like many other hormones, CGRP circulates in plasma with a circadian rhythm. There seems to be a temporal sequence starting with the nocturnal rise in plasma CGRP concentrations and progressing with the ensuing elevations of ANP, PRA, PA, and PC, whereas BP and HR are kept to their lowest values. These findings are in favor of a physiological role of CGRP in the complex regulation of BP homeostasis.
引用
收藏
页码:945 / 951
页数:7
相关论文
共 55 条
[41]   CALCITONIN GENE-RELATED PEPTIDE AND CALCITONIN IN MEDULLARY-THYROID CARCINOMA [J].
SCHIFTER, S ;
WILLIAMS, ED ;
CRAIG, RK ;
HANSEN, HH .
CLINICAL ENDOCRINOLOGY, 1986, 25 (06) :703-710
[42]   SPECIFIC RECEPTOR AND CARDIOVASCULAR EFFECTS OF CALCITONIN GENE-RELATED PEPTIDE [J].
SIGRIST, S ;
FRANCOCERECEDA, A ;
MUFF, R ;
HENKE, H ;
LUNDBERG, JM ;
FISCHER, JA .
ENDOCRINOLOGY, 1986, 119 (01) :381-389
[43]  
SIREN AL, 1988, J PHARMACOL EXP THER, V247, P69
[44]   INCREASED CONCENTRATION OF CIRCULATING CALCITONIN GENE RELATED PEPTIDE DURING NORMAL HUMAN-PREGNANCY [J].
STEVENSON, JC ;
MACDONALD, DWR ;
WARREN, RC ;
BOOKER, MW ;
WHITEHEAD, MI .
BRITISH MEDICAL JOURNAL, 1986, 293 (6558) :1329-1330
[45]   HUMAN CALCITONIN GENE RELATED PEPTIDE - A POTENT ENDOGENOUS VASODILATOR IN MAN [J].
STRUTHERS, AD ;
BROWN, MJ ;
MACDONALD, DWR ;
BEACHAM, JL ;
STEVENSON, JC ;
MORRIS, HR ;
MACINTYRE, I .
CLINICAL SCIENCE, 1986, 70 (04) :389-393
[46]   CALCITONIN GENE-RELATED PEPTIDE IN PATIENTS WITH ENDOCRINE TUMORS [J].
TAKAMI, H ;
SHIKATA, J ;
KAKUDO, K ;
ITO, K .
JOURNAL OF SURGICAL ONCOLOGY, 1990, 43 (01) :28-32
[47]   THE PROPEPTIDE ASN1-TYR126 IS THE STORAGE FORM OF RAT ATRIAL-NATRIURETIC-FACTOR [J].
THIBAULT, G ;
GARCIA, R ;
GUTKOWSKA, J ;
BILODEAU, J ;
LAZURE, C ;
SEIDAH, NG ;
CHRETIEN, M ;
GENEST, J ;
CANTIN, M .
BIOCHEMICAL JOURNAL, 1987, 241 (01) :265-272
[48]   CALCITONIN GENE-RELATED PEPTIDE AND ITS BINDING-SITES IN THE HUMAN CENTRAL NERVOUS-SYSTEM AND PITUITARY [J].
TSCHOPP, FA ;
HENKE, H ;
PETERMANN, JB ;
TOBLER, PH ;
JANZER, R ;
HOKFELT, T ;
LUNDBERG, JM ;
CUELLO, C ;
FISCHER, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (01) :248-252
[49]  
UBERTI ECD, 1979, HORM RES, V10, P64
[50]   INTRADIEM CHANGES OF PLASMA ALDOSTERONE, CORTISOL, CORTICOSTERONE AND GROWTH-HORMONE IN SODIUM RESTRICTION [J].
VAGNUCCI, AH ;
MCDONALD, RH ;
DRASH, AL ;
WONG, AKC .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1974, 38 (05) :761-776