Sac-1004, a Pseudo-Sugar Derivative of Cholesterol, Restores Erectile Function through Reconstruction of Nonleaky and Functional Cavernous Angiogenesis in the Streptozotocin Induced Diabetic Mouse

被引:9
|
作者
Batbold, Dulguun [1 ]
Song, Kang-Moon [1 ]
Park, Jin-Mi [1 ]
Park, Soo-Hwan [1 ]
Lee, Tack [1 ]
Ryu, Dong-Soo [3 ]
Suh, Young-Ger [4 ]
Kwon, Young-Guen [5 ,6 ]
Ryu, Ji-Kan [1 ,2 ]
Suh, Jun-Kyu [1 ]
机构
[1] Inha Univ, Sch Med, Natl Res Ctr Sexual Med, Dept Urol, 7-206 3rd St, Inchon 400711, South Korea
[2] Inha Univ, Sch Med, Inha Res Inst Med Sci, 7-206 3rd St, Inchon 400711, South Korea
[3] Sungkyunkwan Univ, Sch Med, Samsung Changwon Hosp, Dept Urol, Chang Won, South Korea
[4] Seoul Natl Univ, Pharmaceut Sci Res Inst, Seoul, South Korea
[5] Seoul Natl Univ, Coll Pharm, Seoul, South Korea
[6] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Biochem, Seoul 120749, South Korea
关键词
penis; erectile dysfunction; diabetes mellitus; Sac-1004; angiogenesis inducing agents; CORPUS CAVERNOSUM; ENDOTHELIAL DYSFUNCTION; INHIBITION; PATHWAY; BARRIER; LEAKAGE; LDL;
D O I
10.1016/j.juro.2015.12.103
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: We examined whether and how Sac-1004, a vascular leakage blocker, would restore erectile function in an animal model of diabetic erectile dysfunction. Materials and Methods: Eight-week-old C57BL/6J mice were used. Diabetes was induced by intraperitoneal injection of streptozotocin. Eight weeks after diabetes induction the animals were divided into 6 groups, including controls, diabetic mice that received repeat intracavernous injections of phosphate buffered saline (20 mu l) on days -3 and 0, and diabetic mice that received repeat intracavernous injections of Sac-1004 on days -3 and 0 (1, 2, 5 and 10 mu g, respectively, in 20 mu l phosphate buffered saline). One week after injection erectile function was measured by cavernous nerve stimulation. The penis was then harvested for histological examinations and Western blot analysis. Results: Local delivery of Sac-1004 in the corpus cavernosum restored erectile function in diabetic mice. The highest erectile response was noted at a dose of 5 mu g with a response comparable to that in the control group. Sac-1004 significantly increased cavernous endothelial and smooth muscle contents, and induced endothelial nitric oxide synthase phosphorylation (Ser1177). Sac-1004 decreased extravasation of oxidized low density lipoprotein by restoring endothelial cell-cell junction proteins and pericyte content. Sac-1004 also promoted tube formation in primary cultured mouse cavernous endothelial cells in vitro. Sac-1004 mediated cavernous angiogenesis and erectile function recovery was abolished by inhibiting angiopoietin-1-Tie2 signaling with soluble Tie2 antibody. Conclusions: With the effects of angiogenesis and antipermeability Sac-1004 reestablishes structural and functional cavernous sinusoids. This is highly promising for future treatment of erectile dysfunction from vascular causes.
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页码:1936 / 1946
页数:11
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