Melatonin scavenges hydroxyl radical and protects isolated rat hearts from ischemic reperfusion injury

Shinji Kaneko, Kenji Okumura, Yasushi Numaguchi, Hideo Matsui, Kichiro Murase, Shinji Mokuno, Itsuro Morishima, Kenji Hira, Yukio Toki, Takayuki Ito, Tetsuo Hayakawa

Research output: Contribution to journalArticlepeer-review

95 Citations (Scopus)


During postischemic reperfusion, free radicals are produced and have deleterious effects in isolated rat hearts. We investigated whether melatonin (MEL) reduces the production of hydroxyl radical (·OH) in the effluent and aids in recovery of left ventricular (LV) function. Hearts were subjected to 30 min of ischemia followed by 30 min of reperfusion. Salicylic acid (SAL) was used as the probe for ·OH, and its derivatives 2,5- and 2,3- dihydroxybenzoic acid (DHBA) were quantified using HPLC. In addition, thiobarbituric acid reactive substances (TBARS) in the myocardium was measured. Plateaus in the measurement of 2,5- and 2,3-DHBA were seen from 3 to 8 min after reperfusion in each group. The group that received 100 μM MEL+ SAL had significantly reduced amounts of 2,5- and 2,3-DHBA by multiple folds, compared to the SAL group. TBARS was significantly decreased in the 100 μM MEL group (1.20 ± 0.36 vs 1.85 ± 0.10 μmol/g of drug-free group, p<0.001). More importantly, the 100 μM MEL group significantly recovered in LV function (LV developed pressure, +dp/dt, and -dp/dt; 63.0%, 60.3%, and 59.4% in the 100 μM MEL group; 30.2%, 29.7%, and 31.5% in the drug-free group, respectively; p<0.05). Duration of ventricular tachycardia or ventricular fibrillation significantly decreased in the 100 μM MEL group (100 μM MEL, 159 ± 67 sec; drug-free, 1244 ± 233 sec; p<0.05). As a result of scavenging ·OH and reducing the extent of lipid peroxidation, MEL is an effective agent for protection against postischemic reperfusion injury. (C) 2000 Elsevier Science Inc.

Original languageEnglish
Pages (from-to)101-112
Number of pages12
JournalLife Sciences
Issue number2
Publication statusPublished - 02-06-2000
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biochemistry, Genetics and Molecular Biology(all)
  • Pharmacology, Toxicology and Pharmaceutics(all)


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