Cichorium intybus attenuates streptozotocin induced diabetic cardiomyopathy via inhibition of oxidative stress and inflammatory response in rats

Author:

Sharma Manju12,Afaque Aiman1,Dwivedi Shridhar3,Jairajpuri Zeeba S.4,Shamsi Yasmeen5,Khan Mohd Faiyaz6,Khan Mohd Ibrahim7,Ahmed Danish7

Affiliation:

1. Department of Pharmacology, Faculty of Pharmacy , Hamdard University , New Delhi , India

2. Department of Pharmacology, Hamdard Institute of Medical Sciences &Research , Hamdard University , New Delhi , India

3. Department of Medicine and Preventive Cardiology, Hamdard Institute of Medical Sciences &Research , Hamdard University , New Delhi , India

4. Department of Pathology, Hamdard Institute of Medical Sciences &Research , Hamdard University , New Delhi , India

5. Department of Mahiyatul Amraz, Faculty of Medicine (Unani) , Hamdard University , New Delhi , India

6. Department of Clinical Pharmacy , College of Pharmacy , Prince Sattam Bin Abdulaziz University , Al-Kharj , Kingdom of Saudi Arabia

7. Department of Pharmaceutical Sciences , Sam Higginbottom University of Agriculture, Technology & Sciences, (SHUATS) , Allahabad , India

Abstract

Abstract The aim of the present study was to investigate the effects of Cichorium intybus on lipid peroxidation activities of both enzymatic and non-enzymatic antioxidants, inflammatory mediators, myocardial enzymes and histopathology of cardiac tissues in experimental diabetic cardiomyopathy (DCM). DCM was induced by single intraperitoneal injection of streptozotocin (STZ) (40 mg/kg) combined with high energy intake in rats. Seed extract of Cichorium intybus (CIE) (250 mg/kg & 500 mg/kg) was administered orally once a day for 3 weeks. Phytochemical investigations of seed extract revealed presence of some active ingredients such as alkaloids, tannins, saponin, phenols, glycosides, steroids, terpenoids and flavonoids. Seed extract of Cichorium intybus confirmed a significant potency towards restoring the blood glucose, an elevation of the levels of aspartate aminotransferase (AST), lactate dehydrogenase (LDH), superoxide dismutase (SOD), thiobarbituric acid reactive substances (TBARS), blood glutathione (GSH), TNF-α and IL-6 and a reduction in the levels of catalase (CAT) was observed following the STZ treatment. Oxidative stress was accompanied by myocardial degeneration as evidenced by histopathological examination of cardiac tissues. Administration of CIE reduced the lipid peroxides level in heart. Serum levels of AST, GSH, LDH and SOD were brought down to physiological levels by CIE in STZ induced DCM rats. CIE also markedly down-regulated serum TNF-α and IL-6 levels. Catalase that was reduced in serum was brought back to near normal level. The extensive necrotic changes of cardiac tissue by STZ was minimized to normal morphology upon CIE administration. The study demonstrates the cardioprotective effect of CIE via inhibition of oxidative stress and pro-inflammatory cytokines.

Publisher

Walter de Gruyter GmbH

Subject

Health, Toxicology and Mutagenesis,Pharmacology,Toxicology

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