Results of Preclinical Studies of 4-(2-(4-nitrophenyl)-2-oxoethyl)-1-(thietane-3-yl)-1H-1,2,4-triazole-4-th Bromide in Relation to the Hemostasis System <i>in vivo</i>
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Published:2024-02-19
Issue:1
Volume:13
Page:241-246
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ISSN:2658-5049
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Container-title:Drug development & registration
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language:
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Short-container-title:Razrabotka i registraciâ lekarstvennyh sredstv
Author:
Wang Y.1ORCID, Bulatova N. R.2ORCID, Klen E. E.3ORCID, Rozit G. A.3ORCID, Nikitina I. L.3ORCID, Smolyarchuk E. A.4ORCID, Zavadich K. A.4ORCID, Krylova I. D.3ORCID, Samorodov A. V.3ORCID
Affiliation:
1. Hangzhou Normal University 2. The University of Jordan 3. Bashkir State Medical University 4. I. M. Sechenov First MSMU of the Ministry of Health of the Russian Federation (Sechenov University)
Abstract
Introduction. A characteristic manifestation of vascular brain damage is depressive disorders that accompany both acute and chronic disorders of cerebral circulation. Depression not only reduces the patient's quality of life, but also complicates the treatment of basic vascular disease, increases the risk of stroke and death. Therefore, complex therapy of vascular depression includes not only antidepressants, but also basic means to correct the consequences of disorders of cerebral blood flow, including with antiplatelet activity. In this regard, the development of a new molecule based on thietane-containing heterocycles, combining the properties of an antidepressant and an antiplatelet agent.Aim. To conduct a preclinical evaluation of 4-(2-(4-nitrophenyl)-2-oxoethyl)-1-(thietane-3-yl)-1H-1,2,4-triazol-4 bromide when administered to rats.Materials and methods. A study was conducted of the effect of 4-(2-(4-nitrophenyl)-2-oxoethyl)-1-(thietan-3-yl)-1H-1,2,4-triazol-4-bromide on the hemostasis system during intravenous and intragastric administration to healthy white non-linear sexually mature male rats (n = 160). Thromboelastography was performed on a TEG 5000 device, activated with a 0.2 M solution of calcium chloride, Born aggregometry and standard clotting tests to assess the coagulation component of hemostasis.Result and discussion. The findings show that 4-(2-(4-nitrophenyl)-2-oxoethyl)-1-(thietane-3-yl)-1H-1,2,4-triazole-4-th bromide with peroral administration exceeded acetylsalicylic acid by 2.8 times in terms of ED50, and by 1.8 times with intravenous way of administration accordingly. A similar effect of pentoxifylline in the intravenous route of administration was recorded at a concentration of 27.8 mg/kg versus 12.4 mg/kg of compound I. The results of a complex method to assess the state of the hemostasis system indicate a more pronounced antiaggregational effect of compound I compared with pentoxifylline and acetylsalicylic acid.Conclusion. Preclinical studies of 4-(2-(4-nitrophenyl)-2-oxoethyl)-1-(thietane-3-yl)-1H-1,2,4-triazole-4 bromide, was demonstrated that a combination of antidepressant and antiplatelet activity, which can serve as a basis for further drug development.
Publisher
Center of Pharmaceutical Analytics Ltd
Reference30 articles.
1. Andreotti F., Geisler T., Collet J., Gigante B., Gorog D., Halvorsen S., Lip G., Morais J., Navarese E., Patrono C., Rocca B., Rubboli A., Sibbing D., Storey R., Verheugt F., Vilahur G. Acute, periprocedural and longterm antithrombotic therapy in older adults: 2022 Update by the ESC Working Group on Thrombosis. European Heart Journal. 2023;44(4):262–279. DOI: 10.1093/eurheartj/ehac515. 2. Baigent C., Blackwell L., Collins R., Emberson J., Godwin J., Peto R., Buring J., Hennekens C., Kearney P., Meade T., Patrono C., Roncaglioni M., Zanchetti A. Aspirin in the primary and secondary prevention of vascular disease: collaborative meta-analysis of individual participant data from randomised trials. Lancet. 2009;373(9678):1849–1860. DOI: 10.1016/S0140-6736(09)60503-1. 3. Badimon L., Vilahur G., Rocca B., Patrono C. The key contribution of platelet and vascular arachidonic acid metabolism to the pathophysiology of atherothrombosis. Cardiovascular Research. 2021;117(9):2001–2015. DOI: 10.1093/cvr/cvab003. 4. Alenazy F. O., Thomas M. R. Novel antiplatelet targets in the treatment of acute coronary syndromes. Platelets. 2021;32(1):15–28. DOI: 10.1080/09537104.2020.1763731. 5. Patrono C., Bachmann F., Baigent C., Bode C., De Caterina R., Charbonnier B., Fitzgerald D., Hirsh J., Husted S., Kvasnicka J., Montalescot G., García Rodríguez L., Verheugt F., Vermylen J., Wallentin L., Priori S., Alonso Garcia M., Blanc J., Budaj A., Cowie M., Dean V., Deckers J., Fernández Burgos E., Lekakis J., Lindahl B., Mazzotta G., Morais J., Oto A., Smiseth O., Morais J., Deckers J., Ferreira R., Mazzotta G., Steg P., Teixeira F., Wilcox R. Expert consensus document on the use of antiplatelet agents. The task force on the use of antiplatelet agents in patients with atherosclerotic cardiovascular disease of the European society of cardiology. European Heart Journal. 2004;25(2):166–181. DOI: 10.1016/j.ehj.2003.10.013.
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