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An angiotensin II receptor blocker increases sexual behavior in type 2 diabetic mice
Masayoshi Nomura1, Hisae Nishii, Yumi Ozaki
1Department of Urology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan. nomusan@med.uoeh-u.ac.jp
Abstract:
The present study was conducted to examine the effects of olmersartan, angiotensin (ANG) II type 1 (AT(1)) receptor antagonist, on the sexual function in type 2 diabetes model mice. Twenty-week-old KK/Ta mice were used as a model of type 2 diabetes. Age-matched ICR and BALB/C mice were used as non-diabetic controls. The animals were fed powder chow either with or without olmesartan (7.5 microg/g in chow) for 4 weeks. The levels of sexual behavior, activity, and anxiety were then examined between the groups treated with and without olmesartan. The KK/Ta mice treated with olmesartan exhibited a significant increase in the number of mounts and intromission and a decrease in the latency to the first mount in comparison to the KK/Ta mice treated without olmesartan. These effects of olmesartan were not observed in the non-diabetic BALB/C and ICR mice. In addition, the olmesartan treatment did not affect the activity and anxiety regardless of the mouse strain. These findings suggest that the interaction between ANG II and AT(1) receptor may be involved in the pathogenesis of the sexual dysfunction associated with type 2 diabetes and a blockade of ANG II may therefore be a potentially useful treatment for male sexual dysfunction in type 2 diabetes.
Insights
Olmesartan treatment improved sexual function in male type 2 diabetes mice by blocking angiotensin II (ANG II) type 1 (AT(1)) receptors. This suggests a potential therapeutic strategy for diabetic sexual dysfunction.
Area of Science:
- Endocrinology
- Pharmacology
- Urology
Background:
- Type 2 diabetes is associated with male sexual dysfunction.
- The renin-angiotensin system, including angiotensin II (ANG II) and its type 1 (AT(1)) receptor, plays a role in diabetes complications.
Purpose of the Study:
- To investigate the effects of olmesartan, an AT(1) receptor antagonist, on sexual function in a mouse model of type 2 diabetes.
- To determine if blocking the AT(1) receptor can ameliorate sexual dysfunction in type 2 diabetes.
Main Methods:
- KK/Ta mice (type 2 diabetes model) and control mice (ICR, BALB/C) were fed chow with or without olmesartan for 4 weeks.
- Sexual behavior, activity, and anxiety levels were assessed.
- Olmesartan dosage was 7.5 microg/g in chow.
Main Results:
- Olmesartan significantly increased mounting and intromission frequency and decreased latency to first mount in KK/Ta mice.
- These improvements in sexual function were specific to the type 2 diabetes model mice.
- Olmesartan did not affect activity or anxiety levels in any group.
Conclusions:
- The interaction between ANG II and AT(1) receptors is implicated in the pathogenesis of sexual dysfunction in type 2 diabetes.
- Blocking ANG II signaling via AT(1) receptor antagonism may be a promising therapeutic approach for male sexual dysfunction in type 2 diabetes.
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