Activity of angiotensin peptides in clitoral cavernosum of alloxan induced diabetic rabbit

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Objectives: To assess the role of peptides of the angiotensin (ANG) on the regulation of clitoral cavernosum tone and changes in ANG binding affinity in the rabbit with diabetes mellitus. Material and methods: The isometric tension measurement and in vitro autoradiography were used in sham and diabetic clitoral cavernosum. Results: In tension study, contractility in response to ANG I, ANG II, ANG III and ANG IV was enhanced in diabetic clitoral cavernosum strips (EC50 was 67.6 +/- 27.2, 4.3 +/- 0.4, 189.3 +/- 37.3, 443.2 +/- 0.4 nM for diabetic versus 155.2 +/- 76.1, 38.3 +/- 0.1, 528.0 +/- 75.2, 616.9 +/- 69.5 nM for sham, respectively). Contractile responses to ANG II was significantly inhibited by type 1 ANG II receptor (AT1) antagonist but not by type 2 ANG II receptor (AT2) antagonist in both groups. Percentages in contractions by ANG II (1 nM) in the presence of Dup 753 decreased significantly 36.2 +/- 4.6 to 6.3 +/- 2.4% in sham and 56.1 +/- 7.7 to 6.0 +/- 4.8% in diabetic group. The binding affinities were enhanced in diabetic clitoral cavernosum for ANG II (dissociation constant, 4.9 +/- 1.0 for sham versus 0.9 +/- 0.2 nM for diabetic) and for ANG I, ANG III, and ANG IV (inhibitory constant, 28.6 +/- 1.5, 398.7 +/- 157.2, and 3966.5 +/- 1524.1 nM for sham versus 20.6 +/- 5.7, 78.5 +/- 23.7, and 1098.7 +/- 195.5 nM, for diabetic, respectively, all p < 0.05). Sensitivities of AT1 and AT2 receptors to ANG II enhanced in diabetic than sham clitoral cavernosum tissue. Conclusions: This results suggest that the contractile responses to all four ANG peptides are enhanced in the diabetic clitoral cavernosum. Enhancement of contractility in diabetic clitoral cavernosum may be related to the increased affinity to ANG II receptors for ANG peptides. (c) 2005 Elsevier B.V. All rights reserved.
Publisher
ELSEVIER SCIENCE BV
Issue Date
2005-12
Language
English
Article Type
Article
Keywords

ENDOTHELIUM-DEPENDENT RELAXATION; GLYCOSYLATED HUMAN HEMOGLOBIN; SMOOTH-MUSCLE RELAXATION; NITRIC-OXIDE; CORPUS CAVERNOSUM; SYSTEM; DYSFUNCTION; IMPAIRMENT; MECHANISMS; RECEPTORS

Citation

EUROPEAN UROLOGY, v.48, no.6, pp.1042 - 1050

ISSN
0302-2838
DOI
10.1016/j.eururo.2005.06.017
URI
http://hdl.handle.net/10203/92810
Appears in Collection
MSE-Journal Papers(저널논문)
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