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Updated: Aug 19, 2026

Non-invasive Assessment of Microvascular and Endothelial Function
Published on: January 29, 2013
Insulin sensitivity and endothelial function in hypertension: a comparison of temocapril and candesartan
Hirofumi Tomiyama1, Kohki Motobe, Gulnisa Zaydun
1Second Department of Internal Medicine, Tokyo Medical University, Tokyo, Japan. tomiyama@tokyo-med.ac.jp
Insights
Angiotensin-converting enzyme inhibitors (ACEi) improved endothelial function more than angiotensin II receptor blockers (ARB), but both treatments had similar effects on insulin sensitivity in hypertensive patients.
Area of Science:
- Cardiovascular Pharmacology
- Metabolic Disorders
- Hypertension Management
Background:
- Emerging evidence suggests angiotensin-converting enzyme inhibitors (ACEi) may offer superior endothelial function (END) benefits compared to angiotensin II receptor blockers (ARB).
- The differential impact of ACEi and ARB on insulin sensitivity (IS) in hypertensive individuals remains unclear.
- This study investigates the comparative effects of ACEi and ARB on END and IS in patients with hypertension.
Purpose of the Study:
- To compare the efficacy of ACEi versus ARB in modulating endothelial function.
- To assess the impact of ACEi and ARB on insulin sensitivity in hypertensive patients.
- To explore potential biochemical pathways influencing these effects.
Main Methods:
- A crossover study involving 23 hypertensive patients receiving ACEi or ARB for 8-week intervals.
- Endothelial function assessed via forearm blood flow response to reactive hyperemia.
- Insulin sensitivity evaluated using an insulin tolerance test; plasma levels of bradykinin (BK), NOx, tumor necrosis factor-alpha (TNF-alpha), and adiponectin (Adi) were measured.
Main Results:
- ACEi treatment resulted in significantly higher endothelial function, bradykinin (BK), and nitric oxide (NOx) levels compared to ARB.
- Insulin sensitivity and adiponectin (Adi) levels were comparable between ACEi and ARB treatments.
- Tumor necrosis factor-alpha (TNF-alpha) levels were lower following ARB treatment than with ACEi.
Conclusions:
- ACEi and ARB demonstrate similar effects on insulin sensitivity, despite ACEi's more pronounced impact on endothelial function.
- The bradykinin-nitric oxide (BK-NO) pathway may partly explain the enhanced endothelial effects of ACEi.
- Under physiological conditions, endothelial function may not be a primary determinant of insulin sensitivity.
Background:
Recent studies have suggested that angiotensin-converting enzyme inhibitors (ACEi) have a more pronounced effect on endothelial function (END) than angiotensin II receptor blocker (ARB); however, whether this pronounced effect is more beneficial to patients with insulin sensitivity (IS) remains uncertain. The present study compared the effects of ACEi and ARB on END and IS in patients with hypertension.
Methods:
A total of 23 patients with hypertension were given either ACEi or ARB alternatively in a cross-over manner for 8-week intervals. Both END and IS were examined after each treatment period; END was assessed by the response of forearm blood flow to reactive hyperemia and IS by an insulin tolerance test. The plasma levels of bradykinin (BK), NOx, tumor necrosis factor (TNF-alpha), and adiponectin (Adi) were also measured after each treatment.
Results:
We found that END, BK, and NOx were higher after the ACEi treatment than after the ARB treatment. Although the IS and the Adi levels were similar after both treatments, the TNF-alpha level was lower after the ARB treatment than after the ACEi.
Conclusions:
We conclude that ACEi and ARB may have similar effects on insulin sensitivity, irrespective of the more pronounced effects of ACEi on endothelial function. The BK-NO pathway might contribute, at least in part, to the pronounced effect of ACEi. On the other hand, the underlying mechanisms affecting insulin sensitivity might differ for both treatments. These results suggest that endothelial function is not a major determinant of insulin sensitivity under physiologic conditions.
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