The effects of Cannabis sativa and cannabinoids on the inhibition of pancreatic lipase - An enzyme involved in obesity
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作者:
Frans, Phelokazi
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Nelson Mandela Univ, Dept Biochem & Microbiol, ZA-6031 Port Elizabeth, South AfricaNelson Mandela Univ, Dept Biochem & Microbiol, ZA-6031 Port Elizabeth, South Africa
Frans, Phelokazi
[1
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Mkabayi, Lithalethu
[2
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Pletschke, Brett I.
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Rhodes Univ, Dept Biochem & Microbiol, Enzyme Sci Programme ESP, ZA-6140 Makhanda, South AfricaNelson Mandela Univ, Dept Biochem & Microbiol, ZA-6031 Port Elizabeth, South Africa
Pletschke, Brett I.
[2
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Frost, Carminita L.
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Nelson Mandela Univ, Dept Biochem & Microbiol, ZA-6031 Port Elizabeth, South AfricaNelson Mandela Univ, Dept Biochem & Microbiol, ZA-6031 Port Elizabeth, South Africa
Frost, Carminita L.
[1
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[1] Nelson Mandela Univ, Dept Biochem & Microbiol, ZA-6031 Port Elizabeth, South Africa
[2] Rhodes Univ, Dept Biochem & Microbiol, Enzyme Sci Programme ESP, ZA-6140 Makhanda, South Africa
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 mu g/mL concentration of CBN and 39 % inhibition at a 25 mu g/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.
机构:
Kyung Hee Univ, Coll Life Sci, Dept Oriental Med Biotechnol, Global Campus, Gyeonggi 17104, South Korea
Kyung Hee Univ, Grad Sch Biotechnol, Global Campus, Gyeonggi 17104, South KoreaKyung Hee Univ, Coll Life Sci, Dept Oriental Med Biotechnol, Global Campus, Gyeonggi 17104, South Korea
Kim, Do Hoon
Park, Yu Hwa
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Kyung Hee Univ, Coll Life Sci, Dept Oriental Med Biotechnol, Global Campus, Gyeonggi 17104, South Korea
Kyung Hee Univ, Grad Sch Biotechnol, Global Campus, Gyeonggi 17104, South KoreaKyung Hee Univ, Coll Life Sci, Dept Oriental Med Biotechnol, Global Campus, Gyeonggi 17104, South Korea
Park, Yu Hwa
Lee, Jung Suk
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Dongkook Pharm Co Ltd, R&D Ctr, Gyeonggi 16229, South KoreaKyung Hee Univ, Coll Life Sci, Dept Oriental Med Biotechnol, Global Campus, Gyeonggi 17104, South Korea
Lee, Jung Suk
Jeong, Hyun Il
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Dongkook Pharm Co Ltd, R&D Ctr, Gyeonggi 16229, South KoreaKyung Hee Univ, Coll Life Sci, Dept Oriental Med Biotechnol, Global Campus, Gyeonggi 17104, South Korea
Jeong, Hyun Il
Lee, Kye Wan
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Dongkook Pharm Co Ltd, R&D Ctr, Gyeonggi 16229, South KoreaKyung Hee Univ, Coll Life Sci, Dept Oriental Med Biotechnol, Global Campus, Gyeonggi 17104, South Korea
Lee, Kye Wan
Kang, Tong Ho
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Kyung Hee Univ, Coll Life Sci, Dept Oriental Med Biotechnol, Global Campus, Gyeonggi 17104, South Korea
Kyung Hee Univ, Grad Sch Biotechnol, Global Campus, Gyeonggi 17104, South KoreaKyung Hee Univ, Coll Life Sci, Dept Oriental Med Biotechnol, Global Campus, Gyeonggi 17104, South Korea
机构:
Monash Univ Malaysia, Jeffrey Cheah Sch Med & Hlth Sci, Pharmacol Unit, Jalan Lagoon Selatan,Bandar Sunway, Subang Jaya 47500, Selangor, Malaysia
Sunway Univ, Sch Med & Life Sci, Div Pharmacol, Sunway 47500, MalaysiaMonash Univ Malaysia, Jeffrey Cheah Sch Med & Hlth Sci, Pharmacol Unit, Jalan Lagoon Selatan,Bandar Sunway, Subang Jaya 47500, Selangor, Malaysia
Subramaniyan, Vetriselvan
Hanim, Yusoff Umul
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Sunway Univ, Sch Med & Life Sci, Div Pharmacol, Sunway 47500, MalaysiaMonash Univ Malaysia, Jeffrey Cheah Sch Med & Hlth Sci, Pharmacol Unit, Jalan Lagoon Selatan,Bandar Sunway, Subang Jaya 47500, Selangor, Malaysia