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The effects of anti-obesity intervention with orlistat and sibutramine on microvascular endothelial function
Belqes Abdullah Mohammad Al-Tahami1, Ab Aziz Al-Safi Ismail2, Yvonne Tee Get Bee3
1Pharmacology Vascular Laboratory, School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu, Malaysia.
Insights
Orlistat treatment significantly improved microvascular endothelial function in obese patients, associated with weight loss and improved cardiovascular markers. Sibutramine showed no effect on endothelial function.
Area of Science:
- Cardiovascular Medicine
- Metabolic Disorders
- Pharmacology
Background:
- Obesity is linked to impaired microvascular endothelial function.
- Understanding the impact of anti-obesity medications on vascular health is crucial.
Purpose of the Study:
- To evaluate the effects of orlistat and sibutramine on microvascular endothelial function.
- To assess changes in anthropometric measures, lipid profiles, blood pressure (BP), and heart rate (HR).
Main Methods:
- A 9-month randomized trial involving 76 obese subjects.
- Treatment groups received either orlistat or sibutramine.
- Microvascular endothelial function assessed via laser Doppler fluximetry and iontophoresis (acetylcholine and sodium nitroprusside).
Main Results:
- Orlistat treatment led to significant improvements in endothelium-dependent vasodilation (AChmax, ACh % change, ACh peak).
- Orlistat also reduced weight, BMI, BP, HR, total cholesterol, and LDL cholesterol.
- Sibutramine treatment did not improve microvascular endothelial function and increased HR.
Conclusions:
- Orlistat effectively improves microvascular endothelial function in obese individuals.
- The benefits of orlistat are linked to weight reduction and improvements in cardiovascular risk factors.
- Sibutramine lacks beneficial effects on microvascular endothelial function.
Introduction:
Obesity is associated with impaired microvascular endothelial function. We aimed to determine the effects of orlistat and sibutramine treatment on microvascular endothelial function, anthropometric and lipid profile, blood pressure (BP), and heart rate (HR).
Methods:
76 subjects were recruited and randomized to receive orlistat 120 mg three times daily or sibutramine 10 mg daily for 9 months. Baseline weight, BMI, BP, HR and lipid profile were taken. Microvascular endothelial function was assessed using laser Doppler fluximetry and iontophoresis process. Maximum change (max), percent change (% change) and peak flux (peak) in perfusion to acetylcholine (ACh) and sodium nitroprusside (SNP) iontophoresis were used to quantify endothelium dependent and independent vasodilatations.
Results:
24 subjects in both groups completed the trial. After treatment, weight and BMI were decreased for both groups. AChmax, ACh % change and ACh peak were increased in orlistat-treated group but no difference was observed for sibutramine-treated group. BP and total cholesterol (TC) were reduced for orlistat-treated group. HR was reduced for orlistat-treated group but was increased in sibutramine-treated group.
Conclusion:
9 months treatment with orlistat significantly improved microvascular endothelial function. This was associated with reductions in weight, BMI, BP, HR, TC and low density lipoprotein cholesterol. No effect was seen in microvascular endothelial function with sibutramine.
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