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Comparative electrophysiological characterization of ammodytoxin A, a ß-neurotoxin from the nose-horned viper venom, and its enzymatically inactive mutant.
Zuzek, M C; Ivanusec, A; Herman, J; Sribar, J; Leonardi, A; Frangez, R; Krizaj, I.
Affiliation
  • Zuzek MC; Institute of Preclinical Sciences, Veterinary Faculty, Gerbiceva 60, University of Ljubljana, Ljubljana, Slovenia. Electronic address: monika.zuzek@vf.uni-lj.si.
  • Ivanusec A; Department of Molecular and Biomedical Sciences, Jozef Stefan Institute, Jamova cesta 39, Ljubljana, Slovenia. Electronic address: adrijan.ivanusec@gmail.com.
  • Herman J; Institute of Preclinical Sciences, Veterinary Faculty, Gerbiceva 60, University of Ljubljana, Ljubljana, Slovenia. Electronic address: hermanjulija@gmail.com.
  • Sribar J; Department of Molecular and Biomedical Sciences, Jozef Stefan Institute, Jamova cesta 39, Ljubljana, Slovenia. Electronic address: jernej.sribar@ijs.si.
  • Leonardi A; Department of Molecular and Biomedical Sciences, Jozef Stefan Institute, Jamova cesta 39, Ljubljana, Slovenia. Electronic address: Adrijana.Leonardi@ijs.si.
  • Frangez R; Institute of Preclinical Sciences, Veterinary Faculty, Gerbiceva 60, University of Ljubljana, Ljubljana, Slovenia. Electronic address: robert.frangez@vf.uni-lj.si.
  • Krizaj I; Department of Molecular and Biomedical Sciences, Jozef Stefan Institute, Jamova cesta 39, Ljubljana, Slovenia. Electronic address: igor.krizaj@ijs.si.
Toxicon ; 247: 107833, 2024 Aug 28.
Article in En | MEDLINE | ID: mdl-38942241
ABSTRACT
Presynaptic- or ß-neurotoxicity of secreted phospholipases A2 (sPLA2) is a complex process. For full expression of ß-neurotoxicity, the enzymatic activity of the toxin is essential. However, it has been shown that not all toxic effects of a ß-neurotoxin depend on its enzymatic activity, for example, the inhibition of mitochondrial cytochrome c oxidase. The main objective of this study was to verify whether it is possible to observe and study the phospholipase-independent actions of ß-neurotoxins by a standard ex vivo twitch-tension experimental approach. To this end, we compared the effects of a potent snake venom ß-neurotoxin, ammodytoxin A (AtxA), and its enzymatically inactive mutant AtxA(D49S) on muscle contraction of the mouse phrenic nerve-hemidiaphragm preparation. While AtxA significantly affected the amplitude of the indirectly evoked isometric muscle contraction, the resting tension of the neuromuscular (NM) preparation, the amplitude of the end-plate potential (EPP), the EPP half decay time and the resting membrane potential, AtxA(D49S) without enzymatic activity did not. From this, we can conclude that the effects of AtxA independent of enzymatic activity cannot be studied with classical electrophysiological measurements on the isolated NM preparation. Our results also suggest that the inhibition of cytochrome c oxidase activity by AtxA is not involved in the rapid NM blockade by this ß-neurotoxin, but that its pathological consequences are rather long-term. Interestingly, in our experimental setup, AtxA upon direct stimulation reduced the amplitude of muscle contraction and induced contracture of the hemidiaphragm, effects that could be interpreted as myotoxic.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viper Venoms Limits: Animals Language: En Journal: Toxicon Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viper Venoms Limits: Animals Language: En Journal: Toxicon Year: 2024 Document type: Article