INSULIN-LIKE GROWTH FACTOR-I IN INITIAL RENAL HYPERTROPHY IN POTASSIUM-DEPLETED RATS

被引:36
作者
FLYVBJERG, A
MARSHALL, SM
FRYSTYK, J
RASCH, R
BORNFELDT, KE
ARNQVIST, H
JENSEN, PK
PALLESEN, G
ORSKOV, H
机构
[1] AARHUS KOMMUNE HOSP, IMMUNOHISTOL LAB, DK-8000 AARHUS, DENMARK
[2] AARHUS UNIV, INST EXPTL CLIN RES, DK-8000 AARHUS, DENMARK
[3] AARHUS UNIV, INST ANAT, DEPT CELL BIOL, DK-8000 AARHUS, DENMARK
[4] LINKOPING UNIV, DEPT PHARMACOL, S-58185 LINKOPING, SWEDEN
[5] LINKOPING UNIV, DEPT INTERNAL MED, S-58185 LINKOPING, SWEDEN
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1992年 / 262卷 / 06期
关键词
INSULIN-LIKE GROWTH FACTOR-I MESSENGER RNA; HYPOKALEMIA;
D O I
10.1152/ajprenal.1992.262.6.F1023
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We investigated insulin-like growth factor I (IGF-I) in the kidney during the initial renal enlargement induced by dietary K depletion in rats. Kidney weight increase was significant after 3 days of K depletion and amounted to 29% after 7 days compared with pair-fed controls [839 +/- 34 vs. 648 +/- 17 mg (SE), P < 0.01]. The kidney growth occurred despite almost complete arrest in body weight gain in K-depleted animals (8 +/- 3 vs. 34 +/- 4 g/7 days in controls, P < 0.01). Whole kidney protein, RNA, and DNA estimations indicated that cellular hypertrophy during the first 4 days was followed by hyperplasia. Immunoassayable kidney IGF-I concentration increased by 106% (673 +/- 30 vs. 327 +/- 14 ng/g, P < 0.01) in K-depleted animals 24 h after induction of K depletion, stayed elevated until day 4, and returned to control levels on day 7. After K depletion for 24 h, IGF-I immunostaining was markedly increased in the medullary parts of the collecting ducts from K-depleted animals, whereas kidney IGF-I gene expression (IGF-I mRNA) had decreased by 36%. The increase in total kidney IGF-I concentration and immunostainable IGF-I in collecting ducts in kidneys from K-depleted rats precedes the renal hypertrophy and thereby suggests a renotropic role for IGF-I. The increase in kidney IGF-I concentration is not associated with increased IGF-I mRNA levels, indicating that non-transcriptional mechanisms may be responsible for the renal IGF-I accumulation.
引用
收藏
页码:F1023 / F1031
页数:9
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