The effects of Cannabis sativa and cannabinoids on the inhibition of pancreatic lipase – An enzyme involved in obesity

IF 6.9 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Biomedicine & Pharmacotherapy Pub Date : 2024-09-03 DOI:10.1016/j.biopha.2024.117357
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Abstract

Introduction

Obesity is a chronic noncommunicable disease characterized by excessive body fat that can have negative health consequences. Obesity is a complex disease caused by a combination of genetic, environmental, and lifestyle factors. It is characterized by a discrepancy between caloric intake and expenditure. Obesity increases the risk of acquiring major chronic diseases, including heart disease, stroke, cancer, and Type 2 diabetes mellitus (T2DM). Currently, the inhibition of pancreatic lipases (PL) is a promising pharmacological therapy for obesity and weight management. In this study, the inhibition of pancreatic lipase by Cannabis sativa (C. sativa) plant extract and cannabinoids was investigated.

Methods

The inhibitory effect was assessed using p-nitrophenyl butyrate (pNPB), and the results were obtained by calculating the percentage relative activity and assessed using one-way analysis of variance (ANOVA). Kinetic studies and spectroscopy techniques were used to evaluate the mode of inhibition. Diet-induced; and diabetic rat models were studied to evaluate the direct effects of C. sativa extract on PL activity.

Results

Kinetic analyses showed that the plant extracts inhibited pancreatic lipase, with tetrahydrocannabinol (THC) and cannabinol (CBN) being the potential cause of the inhibition noted for the C. sativa plant extract. CBN and THC inhibited the pancreatic lipase activity in a competitive manner, with the lowest residual enzyme activity of 52 % observed at a 10 μg/mL concentration of CBN and 39 % inhibition at a 25 μg/mL concentration of THC. Circular dichroism (CD) spectroscopy revealed that the inhibitors caused a change in the enzyme's secondary structure. At low concentrations, THC showed potential for synergistic inhibition with orlistat. C.sativa treatment in an in vivo rat model confirmed its inhibitory effects on pancreatic lipase activity.

Conclusion

The findings in this study provided insight into the use of cannabinoids as pancreatic lipase inhibitors and the possibility of using these compounds to develop new pharmacological treatments for obesity.

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大麻和大麻素对抑制胰脂肪酶--一种与肥胖有关的酶--的影响。
引言肥胖症是一种慢性非传染性疾病,其特点是体内脂肪过多,会对健康造成负面影响。肥胖症是一种复杂的疾病,由遗传、环境和生活方式等因素共同造成。其特点是热量摄入与消耗之间存在差异。肥胖会增加罹患主要慢性疾病的风险,包括心脏病、中风、癌症和 2 型糖尿病(T2DM)。目前,抑制胰脂肪酶(PL)是治疗肥胖症和控制体重的一种很有前景的药物疗法。本研究调查了大麻(C. sativa)植物提取物和大麻素对胰脂肪酶的抑制作用:方法:使用对硝基苯丁酸酯(pNPB)评估抑制效果,通过计算相对活性百分比得出结果,并使用单因素方差分析(ANOVA)进行评估。动力学研究和光谱技术用于评估抑制模式。研究了饮食诱导的大鼠和糖尿病大鼠模型,以评估荠菜提取物对 PL 活性的直接影响:动力学分析表明,植物提取物对胰脂肪酶有抑制作用,四氢大麻酚(THC)和大麻酚(CBN)是导致荠菜提取物产生抑制作用的潜在原因。CBN 和 THC 以竞争方式抑制胰脂肪酶活性,CBN 浓度为 10 μg/mL 时,酶活性残留最低,为 52%;THC 浓度为 25 μg/mL 时,抑制率为 39%。圆二色性(CD)光谱显示,抑制剂导致酶的二级结构发生变化。在低浓度下,四氢大麻酚显示出与奥利司他协同抑制的潜力。在大鼠体内模型中对 C.sativa 的处理证实了它对胰脂肪酶活性的抑制作用:本研究的发现使人们深入了解了大麻素作为胰脂肪酶抑制剂的用途,以及利用这些化合物开发新的肥胖症药物治疗方法的可能性。
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来源期刊
CiteScore
11.90
自引率
2.70%
发文量
1621
审稿时长
48 days
期刊介绍: Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.
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