Physiology Department, Redeemer's University, Ede, Nigeria.
Physiology Department, University of Ilorin, Ilorin, Nigeria.
Biomed Pharmacother. 2020 Jun;126:110110. doi: 10.1016/j.biopha.2020.110110. Epub 2020 Mar 31.
There is no report in literature on possible physiological changes that accompany dietary modification in obese condition. Moreover, there is no conclusive evidence on the optimal amount of virgin coconut oil (VCO) that could be of health benefit, although it is known to enhance lipid metabolism. Therefore, we investigated the antiobesitogenic action of graded doses of VCO (200, 400 and 600 mg/kg) in obese rats fed with normo/hyper-lipidaemic diet. Sixty rats (n = 10) were divided into 6 groups and treated as follows: the control and high fat diet (HFD) groups were administered normal saline (0.1 mL/day, p.o.) during the last four weeks of the study, and were fed with normal and HFD respectively throughout the twenty weeks duration of the experiment. Groups 3-6 were fed with HFD for 16 weeks, then normal diet during the next 4 weeks. While group - 3 received saline (0.1 mL/day, p.o.) during the last four weeks, groups 4-6 received graded doses of VCO. The results showed that HFD-induced obesity caused impaired glucose homeostasis, distorted hepatic histoarchitecture, selected deviations in hepatic function indices, pro-inflammatory, pro-oxidant, and dsylipidaemic effects. There were evidence of escalated and reversed pathological actions following the replacement of HFD with normal diet. VCO showed no effect on glucose, insulin, insulin resistance, total protein, uric acid and TAC; but equitable effects on CAT, IL-6, CRP, ALT, AST & GGT, irrespective of the dose. Compared to the effects of VCO at 400 and 600 mg/kg, at 200 mg/kg, VCO had more significant therapeutic effects on LDH, MDA, SOD, GPX, TC, TG, LDL-C, total bilirubin, atherogenic and lee indices and hepatic histoarchitecture. Conclusively, VCO, preferably at a low dose could be used to reverse hepatic structural alteration and some biochemical deviations following dietary modifications in obese condition.
目前尚未有文献报道肥胖患者在饮食改变时可能出现的生理变化。此外,尽管已证实初榨椰子油(VCO)可促进脂质代谢,但对于其具有健康益处的最佳剂量仍没有确凿的证据。因此,我们研究了不同剂量(200、400 和 600mg/kg)的 VCO 在喂食正常/高脂血症饮食的肥胖大鼠中的抗肥胖作用。60 只大鼠(n = 10)分为 6 组,如下进行处理:对照组和高脂肪饮食(HFD)组在研究的最后四周给予生理盐水(0.1mL/天,口服),并在实验的 20 周内分别喂食正常饮食和 HFD。第 3-6 组喂食 HFD 16 周,然后在接下来的 4 周内喂食正常饮食。第 3 组在最后四周接受生理盐水(0.1mL/天,口服),而第 4-6 组接受不同剂量的 VCO。结果表明,HFD 诱导的肥胖导致葡萄糖稳态受损、肝组织形态学改变、肝功能指数选择偏差、促炎、促氧化和血脂异常。用正常饮食替代 HFD 后,出现了病理作用加剧和逆转的证据。VCO 对血糖、胰岛素、胰岛素抵抗、总蛋白、尿酸和 TAC 没有影响,但对 CAT、IL-6、CRP、ALT、AST 和 GGT 有同等影响,而与剂量无关。与 400 和 600mg/kg 的 VCO 相比,200mg/kg 的 VCO 对 LDH、MDA、SOD、GPX、TC、TG、LDL-C、总胆红素、致动脉粥样硬化和低脂指数和肝组织形态学有更显著的治疗作用。总之,VCO (最好低剂量)可用于逆转肥胖患者饮食改变后的肝结构改变和一些生化偏差。