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Experimental study of local anesthetic and antiarrhythmic activities of fluorinated ethynylpiperidine derivatives

E.M. SatbayevaAsfendiyarov Kazakh National Medical University, Republic of KazakhstanSymbat ZhumakovaMalika KhaiitovaAsfendiyarov Kazakh National Medical University, Republic of KazakhstanUlan KemelbekovA.B. Bekturov Institute of Chemical Sciences, Republic of Kazakhstan; South Kazakhstan Medical Academy, Republic of KazakhstanF. M. TursunkhodzhaevaS.Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Republic of UzbekistanAzizbek AzamatovS.Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Republic of UzbekistanSh. N. TursymbekAsfendiyarov Kazakh National Medical University, Republic of KazakhstanVahobjon Kh. SabirovTashkent State Technical University, Republic of UzbekistanTalgat NurgozhınAsfendiyarov Kazakh National Medical University, Republic of KazakhstanV. К. YuТ. М. СейлхановShokan Ualikhanov Kokshetau University, Republic of Kazakhstan
ABI

Annotatsiya

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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