雄性大鼠给药过程中1-羟基-1,1-乙基二膦酸加合物和双(2-吡啶-1,2,4-三唑基-3)丙烷镇痛和抗炎活性的评价

I. Cheretaev, M. Ravaeva, E. Chuyan, V. F. Shulgin
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引用次数: 0

摘要

本文报道了1-羟基-1,1-乙基二膦酸加合物与双(2-吡啶-1,2,4-三唑基-3)丙烷(HEA+BPP)在给药21 d的雄性大鼠镇痛和抗炎活性的评价结果。本研究的目的是评价雄性大鼠在给药21天的过程中HEA+BPP给药21天的镇痛和抗炎活性。这些动物被分成7组,每组10只。对40名男性进行了HEA+BPP的镇痛活性测试,对30名男性进行了抗炎活性测试。在HEA+BPP镇痛活性的研究中,以雄性为对照,每天10.00时腹腔注射生理盐水0.2 ml,连续21 d,其余各组同时腹腔注射HEA+BPP,剂量分别为5、50、100 mg/kg,连续21 d。在镇痛研究中,当测试HEA+BPP的抗炎作用时,同样形成动物组,仅不注射100 mg/kg的剂量。HEA+BPP在V. I. Vernadsky克里米亚联邦大学Tauride学院(结构部门)生物和化学系的普通和无机化学系合成。HEA+BPP的化学纯度在98%以上。在实验第1、6、10、14、21天的急性疼痛应激“甩尾”、Randall-Sellitto和“热板”模型中,采用背景和腹腔注射后1 h的疼痛敏感性参数评价HEA+BPP的镇痛活性。在进行甩尾和Randall-Sellitto试验之前,动物注射后被放置在特殊的大鼠保持器中。采用福尔马林足跖水肿试验评价HEA+BPP的抗炎活性。将2%福尔马林溶液以水溶液形式注入大鼠左后腿足底皮下,重现急性炎症反应,并于给予HEA+BPP 5、50 mg/kg剂量的疗程第10、21天采用水容积法测定肢体水肿值。数据以平均值和标准误差平均值表示,使用StatSoft/STATISTICA 8和Graph Pad Prism 7.0软件包进行统计分析。根据文献中给出的关于药物临床前研究结果统计处理的官方方法学建议,使用单因素方差分析(ANOVA)和事后检验Tukey和多重比较Dunn的非参数标准来确定组间差异的显著性。课程执政期间,雄性老鼠头脑+ BPP 21天的剂量范围从5到100毫克/公斤,发现这种化合物主要演示了有效性作为一针止痛,只是机械的痛苦,这种物质与课程管理是有效剂量的5毫克/公斤:«tail-flick»测试表明,使用头脑+ BPP作为止痛剂参与疼痛敏感性的脊髓机制监管建议剂量的5中,50 - 100毫克/公斤只与一个注:潜伏期反应放电的尾巴相对控制的剂量增加5毫克/公斤的第一天他管理+ BPP 32.7% (p≤0.05),剂量为50毫克/公斤1日和21天的政府——40% (p≤0.01)和67.1% (p≤0.001),剂量为100毫克/公斤政府的第一天——80.0% (p≤0.01),分别。给药第10天给药剂量为5 mg/kg时,HEA+BPP有致痛症作用,尾反应放电潜伏期较对照组显著缩短24.1% (p≤0.01)。Randall-Selitto单独使用的效率测试的头脑+ BPP作为机械疼痛镇痛剂量的50和100毫克/公斤(痛阈显著增加相对于控制在25.2% (p≤0.01)和80% (p≤0.01),和在课程管理只有在一个剂量的5毫克/公斤(痛阈显著增加相对于控制(p≤0.001)55.3%,72.5% (p≤0.001)和49.6% (p≤0.01)6日,14日,21天课程的介绍)。“热板”试验表明,HEA+BPP仅以5和50 mg/kg剂量一次性使用作为镇痛药的可行性,因为这些效果在一个疗程的基础上是不稳定和不稳定的。“福尔马林试验”显示HEA+BPP在5 mg/kg剂量下具有炎症和渗出性作用,其中HEA+BPP在给药第21天使大鼠足部福尔马林水肿增加70.9% (p≤0.01)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EVALUATION OF ANALGESIC AND ANTI-INFLAMMATORY ACTIVITY OF 1-HYDROXY-1,1-ETHYLIDENDIPHOSPHONIC ACID ADDUCT AND BIS (2-PYRIDYL-1,2,4-TRIAZOLYL-3)PROPANE DURING COURSE ADMINISTRATION IN MALE RATS
The article presents the results of evaluation of analgesic and anti-inflammatory activity of the adduct of 1-hydroxy-1,1-ethylidendiphosphonic acid and bis(2-pyridyl-1,2,4-triazolyl-3)propane (HEA+BPP) in male rats with a 21-day course administration. The aim of the study was to evaluate analgesic and anti-inflammatory activity in male rats with 21-day course administration of HEA+BPP course administration with 21-day course administration. The animals were divided into 7 groups of 10 individuals. Analgesic activity of HEA+BPP was tested on 40 males, and anti – inflammatory activity was tested on 30 others. In studies of analgesic activity of HEA+BPP, males of one group were control and received intraperitoneal injections of 0.2 ml of saline solution every day at 10.00 for 21 days, the others groups received 0.2 ml of intraperitoneal injections of HEA+BPP at doses of 5, 50 and 100 mg/kg at the same time for 21 days. In analgesic studies, groups of animals were similarly formed, when testing the anti-inflammatory effect of HEA+BPP, only without injecting a dose of 100 mg/kg. HEA+BPP synthesized at the Department of General and inorganic chemistry of the faculty of biology and chemistry of the Tauride Academy (structural division) of the V. I. Vernadsky Crimean Federal University. The chemical purity of HEA+BPP was at least 98 %. The analgesic activity of HEA+BPP was evaluated by the parameters of pain sensitivity of animals in the background and 1 hour after intraperitoneal injections on the 1st, 6th, 10th, 14th and 21st days of the experiment in the models of acute pain stress «tail-flick», Randall-Sellitto and «hot plate». Before the tail-flick and Randall-Sellitto tests were performed, the animals were placed in special rat retainers after injection. The anti-inflammatory activity of HEA+BPP was evaluated in the formalin paw edema test in rats. Acute inflammatory response was reproduced by subplantar injection of 0.1 ml of 2 % formalin solution in the form of an aqueous solution into the left hind leg of a rat, and then the value of limb edema was measured using the method of water plethysmometry on the 10th and 21st days of course administration of HEA+BPP in doses of 5 and 50 mg/kg. The data are presented as mean and standard error mean, statistical analysis performed using the software packages StatSoft/STATISTICA 8 and Graph Pad Prism 7.0. The significance of differences between groups was determined using one-way analysis of variance (ANOVA) with post hoc test Tukey and non-parametric criterion of multiple comparisons of Dunn, according to official methodological recommendations on statistical treatment of the results of preclinical studies of medicines, given in the literature. During course administration to male rats of HEA+BPP for 21 days in the dose range from 5 to 100 mg / kg, it was found that this compound mainly demonstrates effectiveness as an analgesic with a single injection, only for mechanical pain, this substance is effective with a course administration at a dose of 5 mg/kg: The «tail-flick» test showed, that using of HEA+BPP as an analgesic involved in the spinal mechanism of pain sensitivity regulation is advisable in doses of 5, 50 and 100 mg/kg only with a single injection: latent period of the reaction discharge of the tail increased relative to control at a dose of 5 mg/kg on the 1st day of administration of HEA+BPP by 32.7 % (p≤0.05), at a dose of 50 mg/kg on the 1st and 21st days of administration – by 40 % (p≤0.01) and 67.1 % (p≤0.001) and at a dose of 100 mg/kg on the 1st day of administration – by 80.0 % (p≤0.01), respectively. At a dose of 5 mg/kg on the 10th day of administration, on the contrary, was discovered algogenic effect of HEA+BPP (latent period of the reaction discharge of the tail was significantly decreased relative to control by 24.1 % (p≤0.01). In the test of Randall-Selitto the efficiency of single use HEA+BPP as an analgesic in mechanical pain at doses of 50 and 100 mg/kg (pain threshold was significantly increased relative to control at 25.2 % (p≤0.01) and 80 % (p≤0.01), and in course administration only at a dose of 5 mg/kg (pain threshold was significantly increased relative to control at 55.3 % (p≤0.001), 72.5 % (p≤0.001) and 49.6 % (p≤0.01) on the 6th, 14th and 21st day of the course introduction). The «hot plate» test shows the feasibility of only a single use of HEA+BPP as an analgesic in doses of 5 and 50 mg/kg, since these effects were unstable and unstable when administered on a course basis. The «formalin test» revealed the inflammatory and exudative effect of HEA+BPP at a dose of 5 mg/kg, in which HEA+BPP on the 21st day of administration increased the formalin edema of the rat paw by 70.9 % (p≤0.01).
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