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Experimental study of local anesthetic and antiarrhythmic activities of fluorinated ethynylpiperidine derivatives
Satbayeva, E.M.; Zhumakova, S.S.; Khaiitova, M.D.; Kemelbekov, U.S.; Tursunkhodzhaeva, F.M.; Azamatov, A.A.; Tursymbek, Sh.N.; Sabirov, V.Kh.; Nurgozhin, T.S.; Yu, V.K.; Seilkhanov, T.M..
Afiliação
  • Satbayeva, E.M.; Asfendiyarov Kazakh National Medical University. School of General Medicine-1. Department of Pharmacology. Almaty. KZ
  • Zhumakova, S.S.; A.B. Bekturov Institute of Chemical Sciences. Laboratory of Synthetic and Natural Medicinal Compounds Chemistry. Almaty. KZ
  • Khaiitova, M.D.; Asfendiyarov Kazakh National Medical University. School of General Medicine-1. Department of Pharmacology. Almaty. KZ
  • Kemelbekov, U.S.; A.B. Bekturov Institute of Chemical Sciences. Laboratory of Synthetic and Natural Medicinal Compounds Chemistry. Almaty. KZ
  • Tursunkhodzhaeva, F.M.; S.Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan. Department of Pharmacology and Toxicology. Tashkent. UZ
  • Azamatov, A.A.; S.Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan. Department of Pharmacology and Toxicology. Tashkent. UZ
  • Tursymbek, Sh.N.; Asfendiyarov Kazakh National Medical University. School of General Medicine-1. Department of Pharmacology. Almaty. KZ
  • Sabirov, V.Kh.; Tashkent State Technical University. Laboratory of Structural Chemistry. UZ
  • Nurgozhin, T.S.; Asfendiyarov Kazakh National Medical University. School of General Medicine-1. Department of Pharmacology. Almaty. KZ
  • Yu, V.K.; A.B. Bekturov Institute of Chemical Sciences. Laboratory of Synthetic and Natural Medicinal Compounds Chemistry. Almaty. KZ
  • Seilkhanov, T.M.; Shokan Ualikhanov Kokshetau University. Laboratory of Engineering Profile NMR Spectroscopy. KZ
Braz. j. med. biol. res ; 57: e13429, fev.2024. tab, graf
Article em En | LILACS-Express | LILACS | ID: biblio-1568970
Biblioteca responsável: BR1.1
ABSTRACT
The chemical structure of piperidine has a unique ability to combine with other molecular fragments. This fact makes it possible to actively use it as an effective basis for the creation of new drug-like substances. Thus, the aim of the current investigation was to study the acute toxicity, local anesthetic potency, and antiarrhythmic activity of the two new synthesized piperidine derivatives under laboratory codes LAS-286 and LAS-294 (local anesthetic substances). The Bulbring & Wajda animal model and method of determining the nociception threshold during electrical stimulation was used to investigate the action of the substance during infiltration anesthesia. An antiarrhythmic activity was observed by the aconitine-induced rat arrhythmia model. Additionally, these compounds were studied in relation to molecular docking to delineate the structure-activity relationships. The tested piperidine derivatives had a low toxicity in the subcutaneous and intravenous administration routes. The experimental results showed a higher prolonged and pronounced local anesthetic activity for LAS-286 at a 0.5% concentration, compared to the reference preparations. The low dosage of 0.1 mg/kg of LAS-294 demonstrated a pronounced preventive antiarrhythmic effect in 90% of cases on the development of mixed arrhythmia, caused by aconitine. The results of molecular docking confirmed a higher binding affinity of the tested piperidines with the Nav1.4 and Nav1.5 macromolecules. The results of the present study are very promising, because these piperidines have shown a high biological activity, which can suggest a potential therapeutic application in the future.
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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Idioma: En Revista: Braz. j. med. biol. res Assunto da revista: BIOLOGIA / MEDICINA Ano de publicação: 2024 Tipo de documento: Article / Project document País de afiliação: Cazaquistão / Uzbequistão País de publicação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Idioma: En Revista: Braz. j. med. biol. res Assunto da revista: BIOLOGIA / MEDICINA Ano de publicação: 2024 Tipo de documento: Article / Project document País de afiliação: Cazaquistão / Uzbequistão País de publicação: Brasil