Home LiteratureArticle Details
PMID: 9774493 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Lipid peroxidation and antioxidant enzymes in isoproterenol induced oxidative stress in rat tissues.

Pharmacological research ·Vol. 38 ·No. 4 ·1998-10-00 ·Pages 297-303

Rathore N, John S, Kale M, Bhatnagar D

Abstract

The oxidative metabolism of catecholamines produce quinones which react with oxygen to produce superoxide anions (O2-.) and H2O2. The catecholamines, however, are important under stress conditions but may have damaging effects due to the generation of reactive oxygen species (ROS) and formation of oxidation products. ROS are involved as causative factors in many diseases, therefore, the generation of ROS by catecholamines may also contribute to this process. Isoproterenol (ISO) was administered to rats in two doses so as to evaluate their beta-adrenergic and toxicological actions in terms of lipid peroxidation (LPO) and the changes in the antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), glutathione-S-transferase (GST) and glutathione (GSH) content in heart, liver and kidney. ISO treatment caused LPO in tissues, however, the heart initially showed decreased LPO. This is attributed to the condition of hypertrophy by which the heart can protect itself to a limited extent against oxidative stress. The second dose of ISO, administered 24 h after the first treatment, showed toxic effects resulting in a higher increase in LPO. The increased SOD activity in tissues 3 days after a dose of ISO suggests that the ROS may induce SOD activity to dismutate O2-. However, increased amounts of O2-., inhibited SOD activity at 3 and 6 h with recovery towards control values at 12 h of a second dose of ISO treatment. CAT activity in tissues increased at 6 h of a second dose of ISO treatment. The elevated SOD and CAT enzymes in tissues indicate a response due to increased ROS. The increase in GSH content in the heart, liver and kidney at day 2 of ISO treatment and 12 h after the second dose of ISO may also neutralise oxidative stress. The inhibition in GST activity in tissues was observed probably due to increased ROS generation, however, GST activity partially recovered by 12 h after the second dose of ISO, in an attempt to counteract oxidative stress. The result shows that ISO induced oxidative stress and the increase of the antioxidant system in tissues may attenuate oxidative stress. It is suggested that ROS generation in the oxidation of catecholamines may be partially counteracted by the antioxidant system in tissues.

MeSH Terms
Adrenergic beta-Agonists/pharmacology Animals Catalase/drug effects,metabolism Dose-Response Relationship, Drug Female Glutathione/drug effects,metabolism Glutathione Transferase/drug effects,metabolism Heart/drug effects Isoproterenol/pharmacology Kidney/drug effects,enzymology,metabolism Lipid Peroxidation/drug effects Liver/drug effects,enzymology,metabolism Myocardium/enzymology,metabolism Oxidative Stress/drug effects Rats Rats, Wistar Superoxide Dismutase/drug effects,metabolism Time Factors
Chemicals
Adrenergic beta-Agonists Catalase Superoxide Dismutase Glutathione Transferase Glutathione Isoproterenol
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Rathore N
School of Biochemistry, D.A. University, Khandwa Road, Indore, India.
John S
Kale M
Bhatnagar D
Article Info
Journal
Pharmacological research
Abbr.
Pharmacol Res
ISSN
1043-6618
Published
1998-10-00
Pages
297-303
Language
English
Region
Netherlands
NLM ID
8907422
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]