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(非)选择性 NSAIDs 与新斯的明在镇痛和炎症动物模型中的有效相互作用。

The effective interplay of (non-) selective NSAIDs with neostigmine in animal models of analgesia and inflammation.

机构信息

Department of Pharmacology & Therapeutics, Faculty of Pharmacy, Pharos University in Alexandria, Alexandria, Egypt.

Department of Pathology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.

出版信息

BMC Pharmacol Toxicol. 2021 May 1;22(1):24. doi: 10.1186/s40360-021-00488-9.

Abstract

BACKGROUND

Surgical procedures cause perioperative immunosuppression and neuroendocrine stress, exerted by activation of the autonomic nervous system and the hypothalamic-pituitary-adrenal axis. The acetylcholinesterase inhibitor (ACHEI); neostigmine, is known clinically for its analgesic effect in the perioperative phases proving high efficacy; besides possessing anti-inflammatory properties controlling immune cells and cytokine level. Hence, this study evaluated and compared the analgesic and anti-inflammatory activities of the combination of selective Cox-2 inhibitor; celecoxib, with neostigmine versus a combination of the non-selective Cox inhibitor; diclofenac, with neostigmine; in different experimental models of analgesia and inflammation in rats.

METHODS

Analgesic activity of neostigmine with/without diclofenac or celecoxib was assessed in female Sprague-Dawely rats using the tail clip model and acetic acid induced writhing. Serum level of β-endorphin was assessed after the tail clip test. The anti-inflammatory activity was evaluated using acute and sub-chronic formalin induced paw edema. At the end of the sub-chronic formalin test, blood samples were collected for analysis of anti-inflammatory, liver and kidney function markers. Livers, kidneys and hind paws were also examined histopathologically.

RESULTS

Addition of neostigmine to selective or non-selective NSAIDs (celecoxib or diclofenac) causes an increased level of analgesia of NSAIDs with rapid onset of action and short duration, while causing potentiation of the anti-inflammatory effect of neostigmine as seen in the tail clip, writhing, formalin test, Cox-1 and Cox-2 activities, serum β-endorphin, TNF-α, NF-кB and HS-CRP. All combinations of this study disturb some kidney and liver functions, however with normal histopathological appearances, while hind paws reveal improved inflammatory infiltration in all treated groups.

CONCLUSIONS

Selective and non-selective NSAIDs examined in this study could be good adjunct options to general anesthetic agents and neostigmine in perioperative stages, an outcome that needs further clinical investigations.

摘要

背景

手术会引起围手术期免疫抑制和神经内分泌应激,这是由自主神经系统和下丘脑-垂体-肾上腺轴的激活引起的。乙酰胆碱酯酶抑制剂(ACHEI);新斯的明,临床上因其在围手术期的镇痛作用而被证实具有高效性;此外,它还具有抗炎特性,可以控制免疫细胞和细胞因子水平。因此,本研究评估并比较了选择性 COX-2 抑制剂;塞来昔布与新斯的明的组合与非选择性 COX 抑制剂;双氯芬酸,与新斯的明;在不同的镇痛和炎症实验模型中在大鼠中。

方法

使用尾部夹模型和醋酸诱导的扭体实验评估新斯的明与/或与双氯芬酸或塞来昔布联合的镇痛活性。在尾部夹试验后评估血清β-内啡肽水平。使用急性和亚慢性甲醛诱导的爪肿胀评估抗炎活性。在亚慢性甲醛试验结束时,收集血液样本以分析抗炎、肝和肾功能标志物。还检查了肝脏、肾脏和后爪的组织病理学。

结果

将新斯的明加入选择性或非选择性 NSAIDs(塞来昔布或双氯芬酸)中会增加 NSAIDs 的镇痛水平,具有起效快、作用时间短的特点,同时增强新斯的明的抗炎作用,如在尾部夹、扭体、甲醛试验、COX-1 和 COX-2 活性、血清β-内啡肽、TNF-α、NF-κB 和 HS-CRP 中所见。本研究的所有组合都会干扰一些肾脏和肝脏功能,但组织病理学表现正常,而所有治疗组的后爪炎症浸润均有所改善。

结论

在本研究中检查的选择性和非选择性 NSAIDs 可能是围手术期全身麻醉剂和新斯的明的良好辅助选择,这一结果需要进一步的临床研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f1a/8088641/f1aafc1d0fb9/40360_2021_488_Fig1_HTML.jpg

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