Anti-nociceptive and Anti-inflammatory Activity of Synthesized Novel Benzoxazole Derivatives.

Q2 Medicine
Mansi L Patil, Swati S Gaikwad, Naresh J Gaikwad
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引用次数: 1

Abstract

Introduction: Pain is an immunological response to an infection or inflammation and long-term use of pain management therapy includes the use of Nonsteroidal anti-inflammatory drugs, which is associated with the occurrence of toxicity as well as gastrointestinal bleeding. Therefore, the investigation of new analgesic and anti-inflammatory agents remains a major challenge.

Aims: The objective of this research study is to undergo the pharmacological evaluation of newly synthesized benzoxazole derivatives. These novel derivatives were evaluated for anti-nociceptive, anti-inflammatory and cytotoxic activity using various in-vivo and ex-vivo methods Methods: The study was carried out using swiss mice (adult male) weighing between 20gm to 30gm and were divided into groups containing (n=6) six animals in each group for treatment. The anti-nociceptive activity was performed by using 0.1ml of 0.6% v/v acetic acid as nociception inducer and evaluated by the diminished number of abdominal writhes. The anti-inflammatory activity was done using 0.1 ml of 2% w/v Carrageenan induced paw edema method was observed which was evaluated by calculating the percent maximum possible effect. Histopathological evaluation and cytotoxic activity of the compounds were carried out.

Results: The results of this research study revealed that synthesized derivatives (a, b, c, d and e) showed promising anti-nociceptive and anti-inflammatory effects along significantly higher cytotoxic activity in MCF-7 cell lines.

Conclusion: It can be concluded that synthesized derivatives (a, b, c, d and e) have potential anti- nociceptive and anti-inflammatory effects along with cytotoxic activity and certain modification in structure may result in the potent activity.

合成的新型苯并恶唑衍生物的抗伤害和抗炎活性。
疼痛是对感染或炎症的免疫反应,长期使用疼痛管理治疗包括使用非甾体类抗炎药,这与毒性和胃肠道出血的发生有关。因此,研究新的镇痛和抗炎药物仍然是一个重大挑战。目的:对新合成的苯并恶唑衍生物进行药理学评价。方法:选用体重在20 ~ 30gm之间的成年雄性瑞士小鼠,每组(n=6) 6只进行实验。以0.1ml浓度为0.6% v/v的醋酸作为痛觉诱导剂,通过减少腹部扭动次数来评价其抗痛觉活性。采用2% w/v角叉菜胶0.1 ml诱导足跖水肿法观察其抗炎作用,通过计算最大可能效应百分比进行评价。进行了组织病理学评价和细胞毒活性。结果:本研究结果表明,合成的衍生物(a, b, c, d和e)在MCF-7细胞系中显示出良好的抗伤害和抗炎作用,并具有显著较高的细胞毒活性。结论:合成的a、b、c、d和e具有潜在的抗伤害性和抗炎作用,并具有细胞毒活性,在结构上进行一定的修饰可能使其具有较强的活性。
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来源期刊
Anti-Inflammatory and Anti-Allergy Agents in Medicinal Chemistry
Anti-Inflammatory and Anti-Allergy Agents in Medicinal Chemistry Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
3.30
自引率
0.00%
发文量
11
期刊介绍: Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry aims to cover all the latest and outstanding developments in medicinal chemistry and rational drug design for the discovery of new anti-inflammatory & anti-allergy agents. Publishing a series of timely in-depth reviews written by leaders in the field covering a range of current topics, Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments in the field.
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