ALTERATIONS IN RENAL ENDOTHELIN-1 PRODUCTION IN THE SPONTANEOUSLY HYPERTENSIVE RAT

被引:75
作者
HUGHES, AK
CLINE, RC
KOHAN, DE
机构
[1] VET ADM MED CTR, DIV NEPHROL, SALT LAKE CITY, UT 84148 USA
[2] UNIV UTAH, SCH MED, SALT LAKE CITY, UT 84112 USA
关键词
KIDNEY; HYPERTENSION; RENAL; RNA; KIDNEY TUBULES; COLLECTING;
D O I
10.1161/01.HYP.20.5.666
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Endothelin-1 inhibits sodium and water transport systems in the inner medullary collecting duct. Endothelin-1 levels are reduced in the medulla of spontaneously hypertensive rats (SHR), raising the possibility that decreased inner medullary collecting duct production of endothelin-1 could contribute to inappropriate sodium and water retention. In the current study, immunoreactive endothelin-1 was measured in the urine, blood, and eluates from cortex and outer and inner medulla of SHR before (age 3-4 weeks) and after (age 8-9 weeks) the development of hypertension and in age-matched Wistar-Kyoto (WKY) controls. There was no difference in endothelin-1 levels between prehypertensive SHR and WKY rats. In contrast, 8-9-week-old SHR had significantly reduced endothelin-1 in the urine and outer and inner medulla, but not in the cortex or serum compared with those of WKY controls. Furthermore, inner medullary collecting duct cells from 8-9-week-old SHR, either acutely isolated or cultured, released less endothelin-1 than did those from WKY rats. Finally, the level of endothelin-1 messenger RNA was only reduced in the inner medulla and in inner medullary collecting duct cells from 8-9-week-old SHR. In summary, renal medullary, and in particular terminal collecting duct, endothelin-1 production is reduced in SHR only after the development of hypertension. Such decreases in inner medullary collecting duct endothelin-1 production may contribute to the hypertensive state in SHR.
引用
收藏
页码:666 / 673
页数:8
相关论文
共 34 条
  • [1] PAPILLARY COLLECTING TUBULE RESPONSIVENESS TO ATRIAL-NATRIURETIC-FACTOR IN DAHL RATS
    APPEL, RG
    DUNN, MJ
    [J]. HYPERTENSION, 1987, 10 (01) : 107 - 114
  • [2] VASCULAR REACTIVITY, TISSUE-LEVELS, AND BINDING-SITES FOR ENDOTHELIN - A COMPARISON IN THE SPONTANEOUSLY HYPERTENSIVE AND WISTAR-KYOTO RATS
    BOLGER, GT
    LIARD, F
    JODOIN, A
    JARAMILLO, J
    [J]. CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1991, 69 (03) : 406 - 413
  • [3] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [4] CAGNELLI G, 1990, CLIN EXP HYPERTENS A, V12, P1437
  • [6] THE PRIMARY ROLE OF THE KIDNEY AND SALT INTAKE IN THE ETIOLOGY OF ESSENTIAL-HYPERTENSION .1.
    DEWARDENER, HE
    [J]. CLINICAL SCIENCE, 1990, 79 (03) : 193 - 200
  • [7] CELLULAR MECHANISM OF ENDOTHELIN-1 RELEASE BY ANGIOTENSIN AND VASOPRESSIN
    EMORI, T
    HIRATA, Y
    OHTA, K
    KANNO, K
    EGUCHI, S
    IMAI, T
    SHICHIRI, M
    MARUMO, F
    [J]. HYPERTENSION, 1991, 18 (02) : 165 - 170
  • [8] NA-K-ATPASE IN NEPHRON SEGMENTS OF RATS DEVELOPING SPONTANEOUS HYPERTENSION
    GARG, LC
    NARANG, N
    MCARDLE, S
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 249 (06): : F863 - F869
  • [9] ROLE OF ENDOTHELIN IN THE DEVELOPMENT OF DAHL HYPERTENSION
    GOLIGORSKY, MS
    IIJIMA, K
    MORGAN, M
    YANAGISAWA, M
    MASAKI, T
    LIN, L
    NASJLETTI, A
    KASKEL, F
    FRAZER, M
    BADR, KF
    [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1991, 17 : S484 - S491
  • [10] HOFFMAN A, 1990, J AM SOC NEPHROL, V1, P417