Administration of estradiol and progesterone modulate the activities of antioxidant enzyme and aminotransferases in naturally menopausal rats

被引:92
作者
Moorthy, K
Sharma, D
Basir, SF
Baquer, NZ [1 ]
机构
[1] Jawaharlal Nehru Univ, Sch Life Sci, Hormone & Drug Res Lab, New Delhi 110067, India
[2] Jamia Millia Islamia, Dept Biosci, New Delhi 110025, India
关键词
aging; antioxidant; oxidative stress; hormonal replacement therapy; superoxide dismutase; alanine aminotransferase; aspartate aminotransferase;
D O I
10.1016/j.exger.2005.01.004
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
In aging tissues the oxidative stress increases due to decreased activity of antioxidant enzymes and proteolysis increases due to decreased activity of aminotransferases. which can be modified by hormonal replacement therapy (HRT). The aim of the present study was to determine the effect of HRT on the activities of an antioxidant enzyme superoxide dismutase (SOD) and aminotransferases like alanine aminotransferase (Ala-AT) and aspartate aminotransferase in different age groups (12, 18 and 24 months) of naturally menopausal rats. The rats were given the subcutaneous injection of 17 beta-estradiol, progesterone and combination of estradiol and progesterone for 1 month. The activity of SOD, Ala-AT and Asp-AT was measured in the brain (cerebral hemisphere, CH), heart, liver, kidney and uterus. The activity of SOD decreased with age in all the tissues taken particularly in liver. After HRT the enzyme activities were increased as compared to age-matched controls in all the tissues of aging rats. The activities of transaminases (Ala-AT and Asp-AT) showed a decrease with age in all the tissues and administration of estradiol and combination of estradiol and progesterone further decreased both the aminotransferases. Our study elucidates that increased activity of SOD contributes in protection of cells from oxygen toxicity by catalyzing the dismutation of free radicals in tissues. Furthermore. the HRT probably decreases gluconeogenesis and proteolysis by decreasing the activities of Ala-AT and Asp-AT in aging rat tissues. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:295 / 302
页数:8
相关论文
共 49 条
[1]
ABRAHAM GE, 1974, ACTA ENDOCRINOL-COP, V183, P1
[2]
BAQUER NZ, 1993, BIOCHEM MOL BIOL INT, V31, P509
[3]
Bergmeyer H.U., 1974, Methods of Enzymatic Analysis, P752
[4]
Bergmeyer H.U., 1974, Methods of Enzymatic Analysis, P727
[5]
Braunstein A.E., 1973, The Enzymes, P379, DOI 10.1016/S1874-6047(08)60122-5
[6]
STEROID SEX-HORMONES AND MACROPHAGE FUNCTION - MODULATION OF REACTIVE OXYGEN INTERMEDIATES AND NITRITE RELEASE [J].
CHAO, TC ;
VANALTEN, PJ ;
WALTER, RJ .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 1994, 32 (01) :43-52
[7]
THE USE OF PROTEINASES TO DETERMINE THE TOPOLOGICAL LOCATION OF CYTOCHROME-P-450 IN VESICLES DERIVED FROM SMOOTH ENDOPLASMIC-RETICULUM OF RAT-LIVER [J].
COOPER, MB ;
ESTALL, MR ;
RABIN, BR .
BIOCHEMICAL JOURNAL, 1981, 196 (02) :585-589
[8]
LACK OF SEX AND ESTROUS-CYCLE EFFECTS ON THE ACTIVITY OF 3 ANTIOXIDANT ENZYMES IN RATS [J].
DALMEIDA, V ;
HIPOLIDE, DC ;
DASILVAFERNANDES, ME .
PHYSIOLOGY & BEHAVIOR, 1995, 57 (02) :385-387
[9]
DEMOPOULOS HB, 1982, PATHOLOGY OXYGEN, P127
[10]
DHAHBI JM, 1999, ENDOCRINOL METAB, V40, pE260