PHARMACOLOGICAL ACTIVITY OF NEW COMPOSITION WITH A DIMETHYLACETAMIDE DERIVATIVE IN INFRAORBITAL ANESTHESIA IN RATS WITH PERIODONTITIS

Mazov Ya.A., B. E.V., S. E.V., Eliseikina E.V., Dagar E.A., Vavilova O.V., Yurochkina A.M.
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引用次数: 2

Abstract

The safety and local anesthetic activity of the pharmaceutical composition LHT-15-13 containing a dimethylacetamide derivative, an antioxidant and a vasoconstrictor in rats with chronic periodontitis was studied in the work. White laboratory mice were used to determine acute toxicity with intravenous and subcutaneous administration of a 2% aqueous solution of LHT-15-32. In rats with experimental periodontitis, the threshold of pain sensitivity of the second upper molar was determined. The activity of oxidative stress and total antioxidant activity was determined in the mucous membrane of the gums of rats by the method of induced chemiluminescence. Local changes in periodontal tissues were assessed by quantitative enzyme immunoassay. The acute toxicity of the pharmaceutical composition when administered intravenously and subcutaneously was lower than that of the dimethylacetamide derivative with succinic acid LHT-600. LHT-15-13, when administered infraorbitally, caused deep anesthesia that lasted more than 70 minutes, activated the local antioxidant defense system and reduced the level of IL-1β in the gum tissue, caused tissue repair around the impacted upper molar in rats five days after injection. Thus, the pharmaceutical composition can be considered as an effective and safe agent for pain relief of the upper molars in periodontitis.
新组合物与二甲基乙酰胺衍生物在牙周炎大鼠眶下麻醉中的药理活性
本文研究了含二甲基乙酰胺衍生物、抗氧化剂和血管收缩剂的药物组合物LHT-15-13对慢性牙周炎大鼠的安全性和局部麻醉活性。以实验室白鼠为实验对象,观察2% LHT-15-32水溶液静脉和皮下给药的急性毒性。测定实验性牙周炎大鼠第二上磨牙疼痛敏感阈值。采用诱导化学发光法测定大鼠牙龈粘膜氧化应激活性和总抗氧化活性。采用定量酶免疫分析法评估牙周组织局部变化。该药物组合物静脉和皮下给药时的急性毒性低于琥珀酸二甲基乙酰胺衍生物LHT-600。LHT-15-13经眶下给药后,可引起持续70分钟以上的深度麻醉,激活局部抗氧化防御系统,降低牙龈组织中IL-1β水平,并在注射后5 d引起上磨牙周围组织修复。因此,该药物组合物可被认为是缓解牙周炎上颌磨牙疼痛的有效和安全的药物。
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