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N-乙酰半胱氨酸剂量依赖性地提高对乙酰氨基酚在大鼠热板试验中的镇痛效果。

N-acetylcysteine dose-dependently improves the analgesic effect of acetaminophen on the rat hot plate test.

机构信息

Medical Toxicology and Drug Abuse Research Center (MTDRC), Birjand University of Medical Sciences (BUMS), Birjand, Iran.

Cardiovascular Research Center, Birjand University of Medical Sciences, Birjand, Iran.

出版信息

BMC Pharmacol Toxicol. 2021 Jan 7;22(1):4. doi: 10.1186/s40360-020-00469-4.

Abstract

BACKGROUND

Acetaminophen (APAP) induced hepatotoxicity is a clinically important problem. Up to now, interventive therapy with n-acetylcysteine (NAC) has been considered as a gold-standard treatment for APAP overdose. However, no study has focused on the efficacy of these drugs' concurrent administration on probable enhancing therapeutic outcomes. Thus, this study was aimed to investigate the analgesic effect of co-administration of NAC and acetaminophen in male rats. The NAC-APAP drug formulation may demonstrate the stranger antinociceptive effect.

METHODS

Forty-eight male Sprague-Dawley rats (12-14 weeks) randomly divided into six equal groups; control, APAP (received 300 mg/kg APAP), NAC (received 600 mg/kg NAC) and APAP+ NAC groups that received simultaneously 300 mg/kg APAP with 200-600 mg/kg NAC (AN200, AN400, AN600). All administrations were done orally for once. The antinociceptive effect was recorded by measurement of latency period on a hot plate in 30, 60, and 90 min after administrations.

RESULTS

The results showed that NAC's concurrent administration with APAP, dose-dependently increased APAP analgesic effects (p< 0.0001). Moreover, NAC treatment exhibited an antinociceptive effect in 60 and 90 min, per se. The treatments had no adverse effect on liver enzymes and oxidative stress.

CONCLUSION

Co-administration of NAC with APAP can improve the antinociceptive effect of APAP. It is suggested that this compound can enhance analgesic effects of APAP and eventually lead to a reduction in acetaminophen dose. Further studies are needed to evaluate the molecular mechanism of this hyper analgesic effect.

摘要

背景

对乙酰氨基酚(APAP)诱导的肝毒性是一个临床重要问题。到目前为止,用 N-乙酰半胱氨酸(NAC)进行干预治疗已被认为是治疗 APAP 过量的金标准。然而,尚无研究关注这些药物同时给药对提高治疗效果的可能性。因此,本研究旨在探讨 NAC 和对乙酰氨基酚同时给药对雄性大鼠的镇痛效果。NAC-APAP 药物制剂可能表现出更奇特的抗伤害感受作用。

方法

48 只雄性 Sprague-Dawley 大鼠(12-14 周)随机分为六组,对照组、APAP(给予 300mg/kg APAP)、NAC(给予 600mg/kg NAC)和 APAP+NAC 组,同时给予 300mg/kg APAP 加 200-600mg/kg NAC(AN200、AN400、AN600)。所有给药均为口服一次。给药后 30、60 和 90 分钟测量热板潜伏期记录镇痛效果。

结果

结果表明,NAC 与 APAP 同时给药,剂量依赖性地增加了 APAP 的镇痛作用(p<0.0001)。此外,NAC 治疗本身在 60 和 90 分钟时表现出镇痛作用。这些治疗对肝酶和氧化应激没有不良影响。

结论

NAC 与 APAP 同时给药可增强 APAP 的镇痛作用。提示该化合物可增强 APAP 的镇痛作用,最终导致对乙酰氨基酚剂量减少。需要进一步研究来评估这种超镇痛作用的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c574/7791802/9c4c23bbcbce/40360_2020_469_Fig1_HTML.jpg

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