MORPHOLOGY AND FUNCTION OF THE ADRENAL ZONA GLOMERULOSA OF TRANSGENIC RATS TGR [MREN2]27 - EFFECTS OF PROLONGED SODIUM RESTRICTION

被引:13
作者
REBUFFAT, P
ROCCO, S
ANDREIS, PG
NERI, G
NOWAK, KW
PETERS, J
OPOCHER, G
MAZZOCCHI, G
MANTERO, F
NUSSDORFER, GG
机构
[1] UNIV PADUA,DEPT ANAT,I-35121 PADUA,ITALY
[2] UNIV PADUA,DEPT MED SEMEIOL,I-35121 PADUA,ITALY
[3] UNIV HEIDELBERG,DEPT PHARMACOL,D-69120 HEIDELBERG,GERMANY
[4] UNIV ANCONA,DEPT CLIN ENDOCRINOL,I-60100 ANCONA,ITALY
关键词
D O I
10.1016/0960-0760(95)00127-L
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Heterozygous female transgenic rats for the murine Ren-2 gene (TGR) display a high blood pressure, together with a low kidney and high adrenal renin content. The effects of prolonged sodium restriction on the morphology and secretory activity of adrenal zona glomerulosa (ZG) of TGR and their age- and sex-matched Sprague-Dawley control rats (SDR) were investigated. Under basal conditions, TGR had a moderately hypertrophic ZG, that showed a significantly higher secretion of 18-hydroxylated (18OH) steroids: 18-hydroxy-11-deoxycorticosterone (18OH-DOC), 18-hydroxycorticosterone (18OH-B) and aldosterone (ALDO); ZG cells of TGR showed angiotensin II (AII)-binding site concentrations and ALDO secretory responses to AII similar to those of SDR ZG cells. Prolonged sodium restriction increased plasma ALDO level in both SDR and TGR, and significantly raised the volume of ZG. ZG hypertrophy was due to the increase in both the number and average volume of its parenchymal cells. The secretion of 18OH-steroids was markedly enhanced in both groups of rats; however, in TGR this rise was exclusively due to increases of 18OH-DOC and 18OH-B, while in SDR also ALDO production was enhanced. The yield of non-18OH-steroids was not affected. Il-Dehydrocorticosterone production was not changed in SDR, but doubled in TGR. ZG cells of sodium-restricted SDR and TGR displayed similar increases in their AII-binding site concentration and ALDO secretory response to AII. In conclusion, our present findings confirm that TGR possess a hypertrophic ZG and an elevated secretory capacity of 18OH-steroids, but show only slight differences in ZG and ZG-cell responses to prolonged sodium deprivation.
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页码:155 / 162
页数:8
相关论文
共 40 条
[1]   SODIUM RESTRICTION INCREASES ALDOSTERONE BIOSYNTHESIS BY INCREASING LATE PATHWAY, BUT NOT EARLY PATHWAY, MESSENGER-RIBONUCLEIC-ACID LEVELS AND ENZYME-ACTIVITY IN NORMOTENSIVE RATS [J].
ADLER, GK ;
CHEN, R ;
MENACHERY, AI ;
BRALEY, LM ;
WILLIAMS, GH .
ENDOCRINOLOGY, 1993, 133 (05) :2235-2240
[2]   ROLE OF TISSUE RENIN IN THE PATHOPHYSIOLOGY OF HYPERTENSION IN TGR(MREN2)27 RATS [J].
BADER, M ;
ZHAO, Y ;
SANDER, M ;
LEE, MA ;
BACHMANN, J ;
BOHM, M ;
DJAVIDANI, B ;
PETERS, J ;
MULLINS, JJ ;
GANTEN, D .
HYPERTENSION, 1992, 19 (06) :681-686
[3]   REGULATION OF ADRENAL RENIN MESSENGER RIBONUCLEIC-ACID BY DIETARY-SODIUM CHLORIDE [J].
BRECHER, AS ;
SHIER, DN ;
DENE, H ;
WANG, SM ;
RAPP, JP ;
FRANCOSAENZ, R ;
MULROW, PJ .
ENDOCRINOLOGY, 1989, 124 (06) :2907-2913
[4]   THE EFFECT OF LOSARTAN POTASSIUM-STIMULATED ALDOSTERONE SECRETION IN-VITRO [J].
CHIOU, CY ;
KIFOR, I ;
MOORE, TJ ;
WILLIAMS, GH .
ENDOCRINOLOGY, 1994, 134 (06) :2371-2375
[5]   ANALYSIS BY IMMUNOCYTOCHEMISTRY AND INSITU HYBRIDIZATION OF RENIN AND ITS MESSENGER-RNA IN KIDNEY, TESTIS, ADRENAL, AND PITUITARY OF THE RAT [J].
DESCHEPPER, CF ;
MELLON, SH ;
CUMIN, F ;
BAXTER, JD ;
GANONG, WF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (19) :7552-7556
[6]  
DOI Y, 1993, CLIN EXP HYPERTENS A, V5, P1119
[7]   THE ROLE OF LIPOPROTEINS IN STEROIDOGENESIS AND CHOLESTEROL-METABOLISM IN STEROIDOGENIC GLANDS [J].
GWYNNE, JT ;
STRAUSS, JF .
ENDOCRINE REVIEWS, 1982, 3 (03) :299-329
[9]   MODULATION OF ALDOSTERONE SYNTHASE MESSENGER-RIBONUCLEIC-ACID LEVELS BY DIETARY-SODIUM AND POTASSIUM AND BY ADRENOCORTICOTROPIN [J].
HOLLAND, OB ;
CARR, B .
ENDOCRINOLOGY, 1993, 132 (06) :2666-2673
[10]   THE EFFECT OF SODIUM-INTAKE ON ANGIOTENSIN CONTENT OF THE RAT ADRENAL-GLAND [J].
KIFOR, I ;
MOORE, TJ ;
FALLO, F ;
SPERLING, E ;
MENACHERY, A ;
CHIOU, CY ;
WILLIAMS, GH .
ENDOCRINOLOGY, 1991, 128 (03) :1277-1284