Adakudugu Emmanuel A, Ameyaw Elvis O, Obese Ernest, Biney Robert P, Henneh Isaac T, Aidoo Douglas B, Oge Elizabeth N, Attah Isaac Y, Obiri David D
Department of Pharmacology, Faculty of Pharmacy and Pharmaceutical Sciences, Kwame Nkrumah University of Science and Technology (KNUST), Kumasi, Ghana.
School of Pharmacy and Pharmaceutical Sciences, College of Health and Allied Sciences, University of Cape Coast, Cape Coast, Ghana.
Heliyon. 2020 Aug 15;6(8):e04710. doi: 10.1016/j.heliyon.2020.e04710. eCollection 2020 Aug.
Bergapten (5-methoxysporalen) is a furanocoumarin extracted from several species of citrus and bergamot oil. Bergamot essential oil is used traditionally in the management of inflammatory conditions. Previous studies on bergapten have explored mainly its anti-inflammatory activities which include suppression of the expression and release of pro-inflammatory cytokines such as TNF-α and interleukins as well as prostaglandins. Bergapten enhances the clearance of neutrophils and macrophages from the site of inflammation and reduces oxidative stress by inhibition of reactive oxygen species (ROS). Bergapten was assessed for its anti-inflammatory properties in acetic acid-induced colitis. Animals were obtained and randomly placed in six (6) groups (n = 5) after acclimatization. Colitis was induced by rectal administration using 4% / acetic acid in Sprague Dawley rats after pre-treatment for 5 days. Bergapten was administered at doses of 3, 10, and 30 mg kg . while the control group received saline 5 mL kg and the standard drug employed was sulphasalazine at a dose of 500 mg kg. Assessments made for colon-weight-to-length ratio, colonic injury, and mucosal mast cell degranulation. There were reduced colon-weight-to-length ratios in animals treated with bergapten which was significant () for doses 10 and 30 mg kg compared to the disease control group Both macroscopic and microscopic damage were reduced as well, with a lesser percentage of degranulated mast cells. Macroscopic damage was reduced for bergapten at doses 10 and 30 mg kg significantly at and respectively. Similarly, microscopic damage was reduced at and respectively for bergapten 10 and 30 mg kg. The reduction of degranulation by bergapten was significant at . There was generally reduced damage at inflammatory sites as well as decreased infiltration of inflammatory cells. Overall, bergapten reduces inflammation in acetic acid-induced colitis.
补骨脂素(5-甲氧基补骨脂素)是一种从多种柑橘属植物和佛手柑油中提取的呋喃香豆素。传统上,佛手柑精油用于治疗炎症性疾病。先前关于补骨脂素的研究主要探讨了其抗炎活性,包括抑制促炎细胞因子(如肿瘤坏死因子-α和白细胞介素)以及前列腺素的表达和释放。补骨脂素可促进中性粒细胞和巨噬细胞从炎症部位清除,并通过抑制活性氧(ROS)来降低氧化应激。在乙酸诱导的结肠炎中评估了补骨脂素的抗炎特性。动物购得后,适应环境5天后随机分为6组(每组n = 5)。在预处理5天后,通过向Sprague Dawley大鼠直肠内注射4%乙酸诱导结肠炎。补骨脂素的给药剂量为3、10和30 mg/kg。而对照组接受5 mL/kg的生理盐水,使用的标准药物为柳氮磺胺吡啶,剂量为500 mg/kg。评估结肠重量与长度比、结肠损伤和黏膜肥大细胞脱颗粒情况。与疾病对照组相比,用补骨脂素治疗的动物结肠重量与长度比降低,10和30 mg/kg剂量组差异显著(P<0.05)。宏观和微观损伤也均减轻,脱颗粒肥大细胞的百分比降低。补骨脂素10和30 mg/kg剂量组的宏观损伤分别在P<0.叭和P<0.001时显著减轻。同样,补骨脂素10和30 mg/kg剂量组的微观损伤分别在P<0.05和P<0.01时减轻。补骨脂素在P<0.05时对脱颗粒的减少具有显著意义。炎症部位的损伤总体上减少,炎症细胞浸润也减少。总体而言,补骨脂素可减轻乙酸诱导的结肠炎中的炎症。