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S- and P-type cobra venom cardiotoxins differ in their action on isolated rat heart
Averin, Alexey S; Goltyaev, Mikhail V; Andreeva, Tatyana V; Starkov, Vladislav G; Tsetlin, Victor I; Utkin, Yuri N.
Afiliação
  • Averin, Alexey S; Institute of Cell Biophysics. Federal Research Center "Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences". Pushchino. RU
  • Goltyaev, Mikhail V; Institute of Cell Biophysics. Federal Research Center "Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences". Pushchino. RU
  • Andreeva, Tatyana V; Shemyakin­Ovchinnikov Institute of Bioorganic Chemistry. Russian Academy of Sciences. Moscow. RU
  • Starkov, Vladislav G; Shemyakin­Ovchinnikov Institute of Bioorganic Chemistry. Russian Academy of Sciences. Moscow. RU
  • Tsetlin, Victor I; Shemyakin­Ovchinnikov Institute of Bioorganic Chemistry. Russian Academy of Sciences. Moscow. RU
  • Utkin, Yuri N; Shemyakin­Ovchinnikov Institute of Bioorganic Chemistry. Russian Academy of Sciences. Moscow. RU
J. venom. anim. toxins incl. trop. dis ; 28: e20210110, 2022. graf
Article em En | VETINDEX | ID: biblio-1395930
Biblioteca responsável: BR68.1
ABSTRACT

Background:

The cardiovascular system is one of the first systems to be affected by snake toxins; but not many toxins exert a direct effect on the heart. Cobra venom cardiotoxins are among those few toxins that attack the heart. Although the two cardiotoxin types (S and P) differ in their central-loop structure, it is not known whether they differ in their effect on the mammalian heart. We compared the effects of S- and P-type cardiotoxins, CTÐ¥-1 and CTÐ¥-2, respectively, from the cobra Naja oxiana, on the isolated rat heart.

Methods:

An isolated rat heart perfused according to the Langendorff technique was used in this study to investigate the activity of cardiotoxins CTX-1 and CTX-2. The following parameters were registered the left ventricular developed pressure, calculated as the difference between systolic and diastolic pressure in the left ventricle, the end-diastolic pressure, the heart rate, time to maximal end-diastolic pressure (heart contracture), and time to depression of the heart contraction.

Results:

Both cardiotoxins at the concentration of 5 µg/mL initially produce a slight increase in systolic intraventricular pressure, followed by its rapid decrease with a simultaneous increase in diastolic intraventricular pressure until reaching contracture. CTX-2 blocks cardiac contractions faster than CTX-1; in its presence the maximum diastolic pressure is reached faster and the magnitude of the developed contracture is higher.

Conclusion:

The P-type cardiotoxin CTX-2 more strongly impairs rat heart functional activity than the S-type cardiotoxin CTX-1, as expressed in its faster blockage of cardiac contractions as well as in more rapid development and greater magnitude of contracture in its presence.(AU)
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Texto completo: 1 Base de dados: VETINDEX Idioma: En Revista: J. venom. anim. toxins incl. trop. dis Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: VETINDEX Idioma: En Revista: J. venom. anim. toxins incl. trop. dis Ano de publicação: 2022 Tipo de documento: Article