Ameliorative effect of nano-pregabalin in gastrocnemius muscle of gamma irradiated rats with an experimental model of fibromyalgia: Crosstalk of Sirt3, IL-1β and PARP1 pathways

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY Toxicology and applied pharmacology Pub Date : 2024-09-01 Epub Date: 2024-07-14 DOI:10.1016/j.taap.2024.117037
Esraa M. Samy, Rasha R. Radwan, Farag M. Mosallam, Heba A. Mohamed
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Abstract

Background

Fibromyalgia (FM) is a complex syndrome with somatic symptoms connected to the operational state of muscles. Although radiotherapy is a cornerstone in cancer treatment, it is implicated in the aggravation of FM. Lately, formulation of medicines in nano-forms become of great prominence due to their prospective applications in medicine. So, this study aimed to assess possible therapeutic benefits of formulating pregabalin in a nono-form (N-PG) for managing FM during exposure to gamma radiation.

Methods

Gamma rays administered in fractionated doses (2 Gy/day) to male rats after one hour of s.c. injection of reserpine (1 mL/kg per day) to induce FM, then treated with single daily dose of (30 mg/kg, p.o.) PG or N-PG for ten successive days. Rats were subjected to behavioral tests, then sacrificed to obtain serum and gastrocnemius muscles.

Results

N-PG significantly antagonized reserpine-induced FM as proved by; the immobility and performance times in forced swim and rotarod performance tests, respectively were restored near to the normal time, serum IL-8 and MCP-1 chemokines were nearby the normal levels, mitigated oxidative stress through increasing total thiol, Sirt3, CAT enzyme and decreasing COX-1, inhibition of inflammation via IL-1β and MIF significant reduction, it possessed anti-apoptotic effect verified by decreasing PARP-1 and increasing Bcl-XL, gastrocnemius muscles had minimal fibrosis levels as seen after Masson trichrome staining. Histopathological results were coincidence with biochemical inspection.

Conclusion

This study identifies N-PG as a novel drug that could be of a value in the management of FM particularly in cancer patients undergoing radiotherapy.

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纳米瑞格巴林对伽马射线照射的纤维肌痛实验模型大鼠腓肠肌的改善作用:Sirt3、IL-1β和PARP1通路的相互作用
背景:纤维肌痛(FM)是一种复杂的综合征,其躯体症状与肌肉的工作状态有关。尽管放疗是癌症治疗的基石,但它也会导致纤维肌痛的加重。最近,纳米药物制剂因其在医学中的应用前景而备受关注。因此,本研究旨在评估将普瑞巴林配制成非纳米形式(N-PG)用于治疗暴露于伽马射线时的 FM 可能带来的治疗效果:方法:雄性大鼠皮下注射瑞舍平(每天 1 mL/kg)一小时后,以分次剂量(2 Gy/天)接受伽马射线照射,诱发 FM,然后连续十天每天单剂量(30 mg/kg,p.o.)普瑞巴林或 N-PG。对大鼠进行行为测试,然后处死大鼠以获取血清和腓肠肌:结果:N-PG 能明显拮抗利血平诱导的 FM,具体表现为血清中的 IL-8 和 MCP-1 趋化因子接近正常水平;通过增加总硫醇、Sirt3、CAT 酶和减少 COX-1,减轻氧化应激;通过显著减少 IL-1β 和 MIF,抑制炎症;通过减少 PARP-1 和增加 Bcl-XL,具有抗凋亡作用;Masson 三色染色后,腓肠肌的纤维化程度极低。组织病理学结果与生化检查结果一致:本研究发现,N-PG 是一种新型药物,可用于治疗 FM,尤其是正在接受放疗的癌症患者。
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来源期刊
CiteScore
6.80
自引率
2.60%
发文量
309
审稿时长
32 days
期刊介绍: Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products. Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged. Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.
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