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黑种草籽油对慢性压迫损伤动物模型的抗伤害感受作用。

Anti-nociceptive effect of black seed oil on an animal model of chronic constriction injury.

作者信息

Talaei Sayyed Alireza, Banafshe Hamid Reza, Moravveji Alireza, Shabani Mohammad, Tehrani Shiva Shirazi, Abed Alireza

机构信息

Physiology Research Center, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, I.R. Iran.

Social Determinants of Health (SDH) Research Center, Kashan University of Medical Sciences, Kashan, I.R. Iran.

出版信息

Res Pharm Sci. 2022 Jul 14;17(4):383-391. doi: 10.4103/1735-5362.350239. eCollection 2022 Aug.

Abstract

BACKGROUND AND PURPOSE

Traditionally, L. has been known as a medical intervention to treat numerous diseases. This study aimed at investigating the antihyperalgesic effect of black seed oil (BSO) in an experimental model of neuropathic pain.

EXPERIMENTAL APPROACH

Chronic constriction injury (CCI) was performed under anesthesia. The sciatic nerve was ligated with four loose ties. Two separate protocols were used to administer BSO. In chronic treatment, rats were given daily doses of BSO (250, 500, and 1000 mg/kg p.o.) from the 1 day until the 21 post-CCI day. While, in acute treatment, BSO (250, 500, and 1000 mg/kg p.o.) was administered only on the 7, 14, and 21 days. CCI and sham groups were given almond oil according to the same schedule. Behavioral scores were determined by evaluation of the paw withdrawal in the plantar, Von Frey, and acetone tests, on the 7, 14, and 21 days.

FINDINGS/RESULTS: Our results showed that CCI leads to significant allodynia and hyperalgesia in the ipsilateral paw after surgery. Chronic administration of BSO (500 and 1000 mg/kg) obviously attenuated heat hyperalgesia and mechanical allodynia. However, daily administration of BSO did not alter cold allodynia. Nevertheless, when BSO was administered, 30 min before the pain assessment tests, hypersensitivity was not improved in the treated animals.

CONCLUSION AND IMPLICATIONS

These results demonstrated BSO can inhibit neuropathic pain progression and suggests a potential use of BSO to manage hyperalgesia and allodynia. However, additional research is necessary to approve BSO effectiveness, in neuropathic pain conditions.

摘要

背景与目的

传统上,L. 一直被视为治疗多种疾病的医学干预手段。本研究旨在探讨黑种草籽油(BSO)在神经性疼痛实验模型中的抗痛觉过敏作用。

实验方法

在麻醉状态下进行慢性缩窄损伤(CCI)。用四条松结扎坐骨神经。采用两种不同方案给予BSO。在慢性治疗中,大鼠从CCI术后第1天至第21天每日给予BSO(250、500和1000 mg/kg口服)。而在急性治疗中,仅在第7、14和21天给予BSO(250、500和1000 mg/kg口服)。CCI组和假手术组按相同给药方案给予杏仁油。在第7、14和21天,通过评估足底撤离、von Frey和丙酮试验中的爪部退缩来确定行为评分。

研究结果

我们的结果表明,CCI导致术后同侧爪部出现明显的痛觉过敏和异常性疼痛。慢性给予BSO(500和1000 mg/kg)明显减轻热痛觉过敏和机械性异常性疼痛。然而,每日给予BSO并未改变冷异常性疼痛。尽管如此,当在疼痛评估试验前30分钟给予BSO时,治疗动物的超敏反应并未改善。

结论与启示

这些结果表明BSO可抑制神经性疼痛进展,并提示BSO在管理痛觉过敏和异常性疼痛方面具有潜在用途。然而,需要进一步研究以证实BSO在神经性疼痛情况下的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39a5/9400468/b1184b015d39/RPS-17-383-g001.jpg

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