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Beneficial Pharmacological Effects of Levosimendan on Antioxidant Status of Acute Inflammation Induced in Paw of Rat: Involvement in Inflammatory Mediators
Author(s) -
Karakus Emre,
Halici Zekai,
Albayrak Abdulmecit,
Bayir Yasin,
Aydin Ali,
Unal Deniz,
Cadirci Elif,
Ferah Irmak,
Odaci Ersan
Publication year - 2013
Publication title -
basic and clinical pharmacology and toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.805
H-Index - 90
eISSN - 1742-7843
pISSN - 1742-7835
DOI - 10.1111/bcpt.12004
Subject(s) - levosimendan , pharmacology , antioxidant , superoxide dismutase , anti inflammatory , carrageenan , inflammation , medicine , inotrope , glutathione , chemistry , biochemistry , enzyme
Abstract Levosimendan ( LEVO ) is a new calcium sensitizer with positive inotropic and vasodilating properties that represents a new pharmacological class of inotropic drugs that stimulate elevated cardiac output. The purpose of this study was to examine anti‐inflammatory effect and antioxidant activity of LEVO in a carrageenan ( CAR )‐induced inflammatory paw oedema rat model. The CAR ‐induced rat groups received LEVO 1, 2 and 3 mg/kg by intraperitonally and indomethacin ( IND ) 25 mg/kg by oral gavage. LEVO inhibited CAR ‐induced paw oedema and suppressed the production of TNF ‐α, IL ‐1 and IL ‐6 at doses of 2 and 3 mg/kg. In contrast to CAR ‐injected paws, 2 and 3 mg/kg doses of LEVO and IND increased superoxide dismutase ( SOD ) activity and also both doses of LEVO , and IND decreased the 8‐isoprostaglandin F 2α (8‐ ISO ) level. A 2 mg/kg dose of LEVO produced 39%, 46%, 61% and 64.7% anti‐inflammatory effects ( p < 0.0001) for the 1st, 2nd, 3rd and 4th hours, respectively. Other results of our current study have shown that SOD and glutathione for CAR ‐injected groups were lower, and 8‐ ISO level was higher than those for the healthy rat group. LEVO may be provided as a pharmacological agent in the prevention or treatment of diseases in which acute or chronic inflammation occurs based on a pathogenic factor.