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Melittin and phospholipase A 2 from bee ( Apis mellifera) venom cause necrosis of murine skeletal muscle in vivo
Journal article   Peer reviewed

Melittin and phospholipase A 2 from bee ( Apis mellifera) venom cause necrosis of murine skeletal muscle in vivo

Charlotte L Ownby, Jennifer R Powell, Ming-shi Jiang, Jeffrey E Fletcher and Jacob R Powell
Toxicon (Oxford), v 35(1), pp 67-80
1997

Abstract

Melittin and phospholipase A 2 (PLA 2) from bee ( Apis mellifera) venom were tested for their ability to induce necrosis of skeletal muscle cells after intramuscular injection into mice. Light and electron microscopic examination of tissue indicated that both melittin (4 μg/g) and bee venom PLA 2 (4 μg/g) caused necrosis of skeletal muscle cells within 30 min after i.m. injection. Early changes in the cells consisted of delta lesions, indicating a ruptured plasma membrane, and hypercontraction of myofibrils. By 24 hr the affected cells appeared as an amorphous mass of disorganized and disrupted myofibrils contained in an intact basal lamina. To ensure that the myotoxic activity of the melittin preparation was not due to contaminating PLA 2 activity, the preparation was treated with p-bromophenacyl bromide ( p-BPB), a known inhibitor of PLA 2 activity. The p-BPB-treated melittin was determined to have no detectable PLA 2 activity using a sensitive muscle cell culture assay, and it still induced myonecrosis, although to a lesser extent and of a slower onset. Additionally, p-BPB treatment of purified bee venom PLA 2 completely inhibited its myotoxic activity. These results indicate that both melittin and bee venom PLA 2 are capable of inducing necrosis of skeletal muscle cells upon i.m. injection, and that the catalytic and myotoxic activities of bee venom PLA 2 are inhibited by p-BPB. Also, melittin and contaminating PLA 2 in the melittin fraction may be acting synergistically to induce a stronger and more rapid myotoxic effect than occurs with either alone.

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Collaboration types
Domestic collaboration
Web of Science research areas
Pharmacology & Pharmacy
Toxicology
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