Eyiiş Esra, Kaygısız Bilgin, Kılıç Fatma Sultan, Ayhancı Adnan
Eskişehir Osmangazi University Faculty of Science and Letters, Department of Biology, Eskişehir, Turkey.
Eskişehir Osmangazi University Faculty of Medicine, Department of Medical Pharmacology, Eskişehir, Turkey.
Turk J Pharm Sci. 2020 Dec 23;17(6):586-592. doi: 10.4274/tjps.galenos.2019.77992.
Safe and effective drugs are still lacking for many pain therapies. In recent years, growing interest has been devoted thus on herbal drugs as an option to identify new pain killers. Based on this, extensive researches are carried out on L. genus due to its therapeutic potency on pain and inflammation therapy. In this study, among species, the antinociceptive effect of Hub.-Mor., and its contributions to nitrergic, serotonergic, or opioidergic pathways as well as its antiinflammatory acitivity were investigated.
Tail clip, tail flick, and hot plate tests were used to determine the central (spinal and supraspinal) antinociceptive effect, while an acetic acid-induced writhing test was used to measure the peripheral antinociceptive effect of the extract (250 and 500 mg/kg). The extract (250 mg/kg) was then combined with nω-nitro-L-arginine methyl ester, cyproheptadine, and naloxone to evaluate its involvement in nitrergic, serotonergic, or opioidergic pathways, respectively. Carrageenan-induced hind paw edema model was used to determine the antiinflammatory effect of the extract (250 mg/kg).
The extract shows central spinal but not central supraspinal antinociceptive effect, and presents peripheral antinociceptive effect. The antinociceptive actions of the extract is largely regulated via targeting the nitrergic pathway, while the opioidergic pathway is partly involved. Further, the extract shows antiinflammatory effect due to the significant inhibitions on the time dependent edema progression and the cytokine (tumor necrosis factor-alfa and interleukin-1beta) productions.
could be stated as a new source with a high beneficial potential in alleviating pain and inflammation.
许多疼痛治疗仍缺乏安全有效的药物。近年来,人们对草药作为识别新型止痛药的一种选择越来越感兴趣。基于此,由于其在疼痛和炎症治疗方面的治疗潜力,对L.属植物进行了广泛研究。在本研究中,在该属植物中,研究了Hub.-Mor.的抗伤害感受作用及其对一氧化氮能、5-羟色胺能或阿片样物质能途径的作用以及其抗炎活性。
采用尾夹法、甩尾法和热板法测定中枢(脊髓和脊髓以上)抗伤害感受作用,同时采用醋酸诱导扭体试验测定提取物(250和500mg/kg)的外周抗伤害感受作用。然后将提取物(250mg/kg)分别与nω-硝基-L-精氨酸甲酯、赛庚啶和纳洛酮联合使用,以评估其分别参与一氧化氮能、5-羟色胺能或阿片样物质能途径的情况。采用角叉菜胶诱导的后爪水肿模型测定提取物(250mg/kg)的抗炎作用。
提取物显示出中枢脊髓而非中枢脊髓以上的抗伤害感受作用,并呈现外周抗伤害感受作用。提取物的抗伤害感受作用主要通过靶向一氧化氮能途径来调节,而阿片样物质能途径部分参与其中。此外,由于对时间依赖性水肿进展和细胞因子(肿瘤坏死因子-α和白细胞介素-1β)产生的显著抑制,提取物显示出抗炎作用。
可以认为是缓解疼痛和炎症的具有高有益潜力的新来源。