Literature DB >> 8342169

Cardiotoxin 1 from cobra (Naja naja atra) venom causes necrosis of skeletal muscle in vivo.

C L Ownby1, J E Fletcher, T R Colberg.   

Abstract

Cardiotoxin 1 from cobra (Naja naja atra) venom was tested for its ability to cause necrosis of skeletal muscle cells after i.m. injection into mice. Light and electron microscopic examination of tissue indicated that the toxin caused necrosis of skeletal muscle as early as 30 min after injection. The plasma membranes of affected cells were ruptured in the area of delta lesions, and the myofibrils were condensed into dense clumps alternating with clear areas containing elements of the sarcotubular system and damaged mitochondria. By 24 hr the affected cells appeared as empty 'bags' containing only remnants of myofibrils and swollen mitochondria. To eliminate the possibility that the necrosis was due to contaminating phospholipase A2 (PLA2) activity of the sample, the sample was treated with p-bromophenacyl bromide (p-BPB), a known inhibitor of PLA2 activity. The p-BPB-treated preparation caused myonecrosis in vivo in mice, and the treatment caused a significant decrease in the release of fatty acids and no detectable lysophospholipid in human muscle cell cultures treated in vitro with the preparation, indicating the lack of PLA2 activity. Additionally, purified PLA2 from the same venom failed to cause myonecrosis in vivo at doses equal to or ten times the estimated contaminating concentration. Thus, it is concluded that cardiotoxin 1 from Naja naja atra venom causes necrosis of skeletal muscle cells in vivo upon i.m. injection.

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Year:  1993        PMID: 8342169     DOI: 10.1016/0041-0101(93)90376-t

Source DB:  PubMed          Journal:  Toxicon        ISSN: 0041-0101            Impact factor:   3.033


  25 in total

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Review 2.  Biotoxins in muscle regeneration research.

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Journal:  Int J Exp Pathol       Date:  2001-02       Impact factor: 1.925

4.  The expression of dystrophin and alpha1-syntrophin during skeletal muscle regeneration.

Authors:  S Hoshino; N Ohkoshi; A Ishii; S Kameya; S Takeda; S Shoji
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

5.  Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturation.

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6.  Characterization of dystrophic calcification induced in mice by cardiotoxin.

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7.  Mitochondrial alterations and oxidative stress in an acute transient mouse model of muscle degeneration: implications for muscular dystrophy and related muscle pathologies.

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Journal:  J Biol Chem       Date:  2013-11-12       Impact factor: 5.157

8.  Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle.

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9.  Mutually exclusive redox forms of HMGB1 promote cell recruitment or proinflammatory cytokine release.

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Journal:  J Exp Med       Date:  2012-08-06       Impact factor: 14.307

10.  Mitochondrial ROS-derived PTEN oxidation activates PI3K pathway for mTOR-induced myogenic autophagy.

Authors:  Jin-Hwan Kim; Tae Gyu Choi; Seolhui Park; Hyeong Rok Yun; Ngoc Ngo Yen Nguyen; Yong Hwa Jo; Miran Jang; Jieun Kim; Joungmok Kim; Insug Kang; Joohun Ha; Michael P Murphy; Dean G Tang; Sung Soo Kim
Journal:  Cell Death Differ       Date:  2018-07-24       Impact factor: 15.828

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