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紫杉醇诱导的神经性疼痛的临床前研究:一项系统综述。

Preclinical research in paclitaxel-induced neuropathic pain: a systematic review.

作者信息

Bacalhau Carolina, Costa-Pereira José Tiago, Tavares Isaura

机构信息

Department of Biomedicine, Unit of Experimental Biology, Faculty of Medicine, University of Porto, Porto, Portugal.

I3S-Institute of Investigation and Innovation in Health, University of Porto, Porto, Portugal.

出版信息

Front Vet Sci. 2023 Dec 18;10:1264668. doi: 10.3389/fvets.2023.1264668. eCollection 2023.

Abstract

INTRODUCTION

Chemotherapy-induced peripheral neuropathy (CIPN) is a common consequence of cancer treatment and pain is a frequent complaint of the patients. Paclitaxel, a cytostatic drug, generates a well-described peripheral nerve injury and neuroinflammation, which may be experimentally mimicked in animal models. We conducted a systematic review analyzing the experimental design, reporting and mechanisms underlying paclitaxel-induced neuropathy in the included studies to establish the perspectives of translation of the current literature in models of CIPN.

METHODS

We elected studies published in Pubmed and Scopus between 1 January 2018 and 3 December 2022.

RESULTS

According to a defined mesh of keywords searched, and after applying exclusion and inclusion criteria, 70 original studies were included and analyzed in detail. Most studies used male Sprague-Dawley rats to induce paclitaxel-induced neuropathy, used low doses of paclitaxel, and the analyzed studies mainly focused at 14-28 days of CIPN. Mechanical nociceptive tests were preferred in the behavioral evaluation. The mechanisms under study were mainly neuroinflammation of peripheral nerves. The overall methodological quality was considered moderate, and the risk of bias was unclear.

DISCUSSION

Despite the ample preclinical research in paclitaxel-induced neuropathy, this systematic review alerts to some flaws in the experimental design along with limitations in reporting, e.g., lack of representation of both sexes in experimental work and the lack of reporting of the ARRIVE guidelines. This may limit the reproducibility of preclinical studies in CIPN. In addition, the clinical features of CIPN should be considered when designing animal experiments, such as sex and age of the CIPN patients. In this way the experimental studies aiming to establish the mechanisms of CIPN may allow the development of new drugs to treat CIPN and translation in the research of CIPN could be improved.

摘要

引言

化疗引起的周围神经病变(CIPN)是癌症治疗的常见后果,疼痛是患者的常见主诉。紫杉醇是一种细胞毒性药物,会导致一种已被充分描述的周围神经损伤和神经炎症,这在动物模型中可以通过实验模拟。我们进行了一项系统评价,分析纳入研究中紫杉醇诱导神经病变的实验设计、报告内容及潜在机制,以确立当前文献在CIPN模型中的转化前景。

方法

我们选取了2018年1月1日至2022年12月3日期间发表在PubMed和Scopus上的研究。

结果

根据搜索的既定关键词网,在应用排除和纳入标准后,纳入并详细分析了70项原始研究。大多数研究使用雄性Sprague-Dawley大鼠诱导紫杉醇诱导的神经病变,使用低剂量紫杉醇,且分析的研究主要聚焦于CIPN的14 - 28天。行为评估中首选机械性伤害感受测试。所研究的机制主要是周围神经的神经炎症。总体方法学质量被认为中等,偏倚风险不明确。

讨论

尽管在紫杉醇诱导神经病变方面有大量临床前研究,但这项系统评价提醒人们注意实验设计中的一些缺陷以及报告方面的局限性,例如实验工作中缺乏两性代表性以及未报告ARRIVE指南。这可能会限制CIPN临床前研究的可重复性。此外,在设计动物实验时应考虑CIPN的临床特征,如CIPN患者的性别和年龄。这样,旨在确立CIPN机制的实验研究可能会促进治疗CIPN新药的研发,并改善CIPN研究中的转化情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/085b/10766764/4f68d575b7e8/fvets-10-1264668-g001.jpg

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