含橙皮苷和薯蓣皂苷的微量纯化类黄酮提取物对长春新碱所致大鼠神经病变的影响一氧化氮途径的作用

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Iranian Journal of Pharmaceutical Research Pub Date : 2024-11-02 eCollection Date: 2025-01-01 DOI:10.5812/ijpr-154455
Nikoo Abharian, Nima Naderi, Noushin Nikray, Mona Khoramjouy, Shokoofe Noori, Hamed Shafaroodi, Mehrdad Faizi
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引用次数: 0

摘要

背景:化疗诱导的周围神经病变(CIPN)是癌症化疗后可能发生的潜在并发症。目的:长春新碱引起的CIPN是一种痛苦且常见的并发症,由于医疗干预措施有限,因此需要进一步研究CIPN的发生机制,并制定有效的预防和治疗策略。方法:以0.1 mg/kg剂量长春新碱(VCR)腹腔注射10 d,诱导雄性Wistar大鼠发生CIPN。处理涉及含有橙皮苷和薯蓣皂苷(MPFF)的微粉纯化类黄酮组分(MPFF);Daflon®),剂量分别为50、100和200 mg/kg。我们的研究集中在背根神经节(DRG)组织中的炎症因子(TNF-α, IL-6)水平,并包括一系列行为测试:Von Frey、握力、旋转杆、空地和热板测试。为了研究一氧化氮(NO)通路在MPFF对vcr诱导的周围神经病变(VIPN)中的作用,我们还测试了l -精氨酸(100 mg/kg i.p)作为NO前体和L-NAME (20 mg/kg i.p)作为一氧化氮合酶(NOS)抑制剂的作用。结果:根据我们的行为测试,MPFF(50、100、200 mg/kg)有效减轻了VIPN的一些症状,包括机械异常性痛和痛觉过敏。值得注意的是,100和200 mg/kg MPFF组DRG组织中TNF-α和IL-6水平显著降低。这些结果强调了MPFF的潜力和NO信号通路在减轻VCR引起的神经性疼痛中的作用。结论:微粉化纯化黄酮类成分可能通过降低DRG组织的机械异常性痛、热痛觉过敏和TNF-α和IL-6水平,有效治疗VIPN。NO通路可能在MPFF治疗VIPN的有效性中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of Micronized Purified Flavonoid Fraction Containing Hesperidin and Diosmin on Vincristine-Induced Neuropathy in Rats; the Role of Nitric Oxide Pathway.

Effect of Micronized Purified Flavonoid Fraction Containing Hesperidin and Diosmin on Vincristine-Induced Neuropathy in Rats; the Role of Nitric Oxide Pathway.

Effect of Micronized Purified Flavonoid Fraction Containing Hesperidin and Diosmin on Vincristine-Induced Neuropathy in Rats; the Role of Nitric Oxide Pathway.

Effect of Micronized Purified Flavonoid Fraction Containing Hesperidin and Diosmin on Vincristine-Induced Neuropathy in Rats; the Role of Nitric Oxide Pathway.

Background: Chemotherapy-induced peripheral neuropathy (CIPN) is a potential complication that can develop following cancer chemotherapy.

Objectives: Due to limited medical interventions for the prevention and management of CIPN caused by vincristine, a painful and common complication, further research to find the mechanisms of CIPN and the development of effective preventive and therapeutic strategies is needed.

Methods: We induced CIPN in male Wistar rats by administering intraperitoneal vincristine (VCR) at a dose of 0.1 mg/kg for 10 days. Treatment involved micronized purified flavonoid fraction (MPFF) containing hesperidin and diosmin (MPFF; Daflon®) at doses of 50, 100, and 200 mg/kg. Our investigation focused on levels of inflammatory factors (TNF-α, IL-6) in the dorsal root ganglion (DRG) tissue and included a series of behavioral tests: Von Frey, grip strength, rotarod, open field, and hot plate tests. To examine the role of the nitric oxide (NO) pathway in the effects of MPFF on VCR-induced peripheral neuropathy (VIPN), we also tested the effect of L-arginine (100 mg/kg i.p.) as a NO precursor and L-NAME (20 mg/kg i.p.) as a nitric oxide synthase (NOS) inhibitor.

Results: Based on our behavioral tests, MPFF (50, 100, 200 mg/kg) effectively reduced some symptoms of VIPN, including mechanical allodynia and hyperalgesia. Notably, TNF-α and IL-6 levels in the DRG tissue of the groups treated with 100 and 200 mg/kg of MPFF showed a significant reduction in inflammatory factors. These results underscore the potential of MPFF and the role of the NO signaling pathway in alleviating neuropathic pain caused by VCR.

Conclusions: Micronized purified flavonoid fraction may be an effective treatment for VIPN by reducing mechanical allodynia, thermal hyperalgesia, and TNF-α and IL-6 levels in DRG tissue. The NO pathway may play a role in the effectiveness of MPFF in treating VIPN.

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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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