Differential cloning of growth hormone-regulated hepatic transcripts in the aged rat

被引:27
作者
Tollet-Egnell, P
Flores-Morales, A
Odeberg, J
Lundeberg, J
Norstedt, G
机构
[1] Karolinska Hosp, Karolinska Inst, Dept Mol Med, S-17176 Stockholm, Sweden
[2] Royal Inst Technol, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
关键词
D O I
10.1210/en.141.3.910
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It has been suggested that aging or at least some of its symptoms are related to a physiological decline in GH levels with age. This study was performed to elucidate age-related changes in GH-dependent effects at the level of gene expression. Through the application of complementary DNA representational difference analysis (RDA) we have identified gene products that are reduced during aging in rat liver. The expression of these genes was restored upon GH treatment. Results from reverse Northern and ribonuclease protection analysis confirmed that the RDA products were truly differentially expressed. In addition to well characterized GH-regulated genes, including CYP2C12, CYP2C13, and alpha(2u)-globulin, we demonstrate the differential expression of at least 11 genes previously not known to be under GH control. Several hepatic transcripts encoding enzymes and receptors involved in the metabolism of protein, carbohydrates, and lipids were identified. Other RDA products consisted of transcripts encoding proteins involved in ATP synthesis, detoxification of reactive oxygen species, or immune responses. This list of GH-regulated genes in the old rat may shed further light on the action and mechanism behind the positive effects of GH on, for example, body composition and the immune system that have been observed in different animal and human studies.
引用
收藏
页码:910 / 921
页数:12
相关论文
共 73 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]  
Angelin Bo, 1994, Current Opinion in Lipidology, V5, P160, DOI 10.1097/00041433-199405030-00002
[3]   STUDIES OF GROWTH-HORMONE SECRETION IN CALORICALLY RESTRICTED DOGS - EFFECT OF CHOLINERGIC AGONISTS AND ANTAGONISTS, GLUCOSE AND THYROTROPIN-RELEASING-HORMONE [J].
ARCE, VM ;
CELLA, SG ;
LOCATELLI, V ;
MULLER, EE .
NEUROENDOCRINOLOGY, 1991, 53 (05) :467-472
[4]   BIOGENESIS OF MITOCHONDRIA [J].
ATTARDI, G ;
SCHATZ, G .
ANNUAL REVIEW OF CELL BIOLOGY, 1988, 4 :289-333
[5]   Metabolic actions of growth hormone: Direct and indirect [J].
Berneis, K ;
Keller, U .
BAILLIERES CLINICAL ENDOCRINOLOGY AND METABOLISM, 1996, 10 (03) :337-352
[6]   CARDIOVASCULAR EFFECTS OF PROLONGED GROWTH-HORMONE REPLACEMENT IN ADULTS [J].
BESHYAH, SA ;
SHAHI, M ;
FOALE, R ;
JOHNSTON, DG .
JOURNAL OF INTERNAL MEDICINE, 1995, 237 (01) :35-42
[7]   The immune-endocrine loop during aging: Role of growth hormone and insulin-like growth factor-I [J].
Burgess, W ;
Liu, Q ;
Zhou, JH ;
Tang, QS ;
Ozawa, A ;
VanHoy, R ;
Arkins, S ;
Dantzer, R ;
Kelley, KW .
NEUROIMMUNOMODULATION, 1999, 6 (1-2) :56-68
[8]  
CHRISTIANSEN JS, 1991, HORM RES, V36, P66
[9]   HUMAN GROWTH-HORMONE AND HUMAN AGING [J].
CORPAS, E ;
HARMAN, SM ;
BLACKMAN, MR .
ENDOCRINE REVIEWS, 1993, 14 (01) :20-39
[10]   CARDIOVASCULAR EFFECTS OF GROWTH-HORMONE TREATMENT IN GROWTH-HORMONE-DEFICIENT ADULTS - STIMULATION OF THE RENIN ALDOSTERONE SYSTEM [J].
CUNEO, RC ;
SALOMON, F ;
WILMSHURST, P ;
BYRNE, C ;
WILES, CM ;
HESP, R ;
SONKSEN, PH .
CLINICAL SCIENCE, 1991, 81 (05) :587-592