Protective effect of hydroxyfasudil, a Rho kinase inhibitor, on ventral prostatic hyperplasia in the spontaneously hypertensive rat. Issue 15 (19th August 2015)
- Record Type:
- Journal Article
- Title:
- Protective effect of hydroxyfasudil, a Rho kinase inhibitor, on ventral prostatic hyperplasia in the spontaneously hypertensive rat. Issue 15 (19th August 2015)
- Main Title:
- Protective effect of hydroxyfasudil, a Rho kinase inhibitor, on ventral prostatic hyperplasia in the spontaneously hypertensive rat
- Authors:
- Holmström, Felix
Shimizu, Shogo
Shimizu, Takahiro
Higashi, Youichirou
Martin, Darryl T.
Honda, Masashi
Saito, Motoaki - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pros23063-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>Rho kinase (ROCK) pathway is associated with various cellular functions, such as smooth muscle contraction, inflammatory response, and cell proliferation. The spontaneously hypertensive rat (SHR) is commonly used genetically hypertensive rat model which develops hyperplastic morphological abnormalities in the ventral prostate. We investigated whether administration of hydroxyfasudil, a ROCK inhibitor, could reduce the levels of growth factors, inflammatory markers, and morphological abnormalities in the ventral prostate of the SHR.</p> </sec> <sec id="pros23063-sec-0002" sec-type="section"> <title>METHODS</title> <p>Twelve‐week‐old SHRs were treated with hydroxyfasudil (1 mg/kg/day, i.p.) or vehicle once daily for another 6 weeks. Wistar Kyoto (WKY) rats treated with vehicle were used as normotensive controls. At 18 weeks of age, blood pressure and heart rate were measured by the tail cuff method. Then the rats were sacrificed, and the ventral prostates were removed. The levels of ROCK activity, growth factors (TGF‐β1 and bFGF), a smooth muscle differentiation marker (α‐SMA) and an inflammatory cytokine (IL‐6) in the ventral prostate were measured by ELISA and western blot. A histological evaluation in each group was also performed.</p> </sec> <sec id="pros23063-sec-0003" sec-type="section"><abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pros23063-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>Rho kinase (ROCK) pathway is associated with various cellular functions, such as smooth muscle contraction, inflammatory response, and cell proliferation. The spontaneously hypertensive rat (SHR) is commonly used genetically hypertensive rat model which develops hyperplastic morphological abnormalities in the ventral prostate. We investigated whether administration of hydroxyfasudil, a ROCK inhibitor, could reduce the levels of growth factors, inflammatory markers, and morphological abnormalities in the ventral prostate of the SHR.</p> </sec> <sec id="pros23063-sec-0002" sec-type="section"> <title>METHODS</title> <p>Twelve‐week‐old SHRs were treated with hydroxyfasudil (1 mg/kg/day, i.p.) or vehicle once daily for another 6 weeks. Wistar Kyoto (WKY) rats treated with vehicle were used as normotensive controls. At 18 weeks of age, blood pressure and heart rate were measured by the tail cuff method. Then the rats were sacrificed, and the ventral prostates were removed. The levels of ROCK activity, growth factors (TGF‐β1 and bFGF), a smooth muscle differentiation marker (α‐SMA) and an inflammatory cytokine (IL‐6) in the ventral prostate were measured by ELISA and western blot. A histological evaluation in each group was also performed.</p> </sec> <sec id="pros23063-sec-0003" sec-type="section"> <title>RESULTS</title> <p>There were significant increases in blood pressure, prostate weight, prostate body weight ratio, and tissue levels of ROCK activity, TGF‐β1, bFGF, α‐SMA, and IL‐6 in the SHR compared to the WKY rat. Histological examination of the ventral prostate showed morphological abnormalities such as a higher degree of proliferation in the glandular epithelial and stromal area in the SHR compared to the WKY rat. Treatment with hydroxyfasudil reduced the elevated ROCK activity, TGF‐β1, bFGF, α‐SMA, and IL‐6 found in the ventral prostate of the SHR. Moreover, treatment with hydroxyfasudil decreased the morphological abnormalies in the SHR ventral prostate.</p> </sec> <sec id="pros23063-sec-0004" sec-type="section"> <title>CONCLUSIONS</title> <p>Treatment with hydroxyfasudil decreased the growth factors, an inflammatory cytokine, and morphological abnormalies in the SHR ventral prostate. These results suggest that chronic treatment with hydroxyfasudil may inhibit the progression of prostatic hyperplasia in the SHR. <italic>Prostate 75:1774–1782, 2015</italic>. © 2015 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Prostate. Volume 75:Issue 15(2015)
- Journal:
- Prostate
- Issue:
- Volume 75:Issue 15(2015)
- Issue Display:
- Volume 75, Issue 15 (2015)
- Year:
- 2015
- Volume:
- 75
- Issue:
- 15
- Issue Sort Value:
- 2015-0075-0015-0000
- Page Start:
- 1774
- Page End:
- 1782
- Publication Date:
- 2015-08-19
- Subjects:
- Prostate -- Diseases -- Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0045 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pros.23063 ↗
- Languages:
- English
- ISSNs:
- 0270-4137
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6935.194000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3486.xml