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Intratunical Injection of Human Adipose Tissue-derived Stem Cells Prevents Fibrosis and Is Associated with Improved Erectile Function in a Rat Model of Peyronies Disease

Castiglione, Fabio (författare)
University of Vita Salute San Raffaele, Milan, Italy
Hedlund, Petter (författare)
Östergötlands Läns Landsting,Linköpings universitet,Klinisk farmakologi,Hälsouniversitetet
Van der Aa, Frank (författare)
Katholieke University of Leuven, Belgium
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Bivalacqua, Trinity J. (författare)
Johns Hopkins Medical Institute, Baltimore, MD, USA
Rigatti, Patrizio (författare)
University of Vita Salute San Raffaele, Milan, Italy
Van Poppel, Hein (författare)
Katholieke University of Leuven, Belgium
Montorsi, Francesco (författare)
University of Vita Salute San Raffaele, Milan, Italy
De Ridder, Dirk (författare)
Katholieke University of Leuven, Belgium
Albersen, Maarten (författare)
University of Vita Salute San Raffaele, Milan, Italy
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 (creator_code:org_t)
Elsevier, 2013
2013
Engelska.
Ingår i: European Urology. - : Elsevier. - 0302-2838 .- 1873-7560. ; 63:3, s. 551-560
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Peyronies disease (PD) is a connective tissue disorder of the tunica albuginea (TA). Currently, no gold standard has been developed for the treatment of the disease in its active phase. less thanbrgreater than less thanbrgreater thanObjective: To test the effects of a local injection of adipose tissue-derived stem cells (ADSCs) in the active phase of a rat model of PD on the subsequent development of fibrosis and elastosis of the TA and underlying erectile tissue. less thanbrgreater than less thanbrgreater thanDesign, setting, and participants: A total of 27 male 12-wk-old Sprague-Dawley rats were divided in three equal groups and underwent injection of vehicle (sham), 50-mu g transforming growth factor (TGF)-beta 1 in a 50-mu l vehicle in either a PD or a PD plus ADSC group in the dorsal aspect of the TA. less thanbrgreater than less thanbrgreater thanIntervention: The sham and PD groups were treated 1 d after TGF-beta 1 injection with intralesional treatment of vehicle, and the PD plus ADSC group received 1 million human-labeled ADSCs in the 50-mu l vehicle. Five weeks after treatment, six rats per group underwent erectile function measurement. Following euthanasia, penises were harvested for histology and Western blot. less thanbrgreater than less thanbrgreater thanOutcome measurements and statistical analysis: The ratio of intracavernous pressure to mean arterial pressure (ICP/MAP) upon cavernous nerve stimulation, elastin, and collagen III protein expression and histomorphometric analysis of the penis. Statistical analysis was performed by analysis of variance followed by the Tukey-Kramer test for post hoc comparisons or the Mann-Whitney test when applicable. less thanbrgreater than less thanbrgreater thanResults and limitations: Erectile function significantly improved after ADSC treatment (ICP/MAP 0.37 in PD vs 0.59 in PD plus ADSC at 5-V stimulation; p = 0.03). PD animals developed areas of fibrosis and elastosis with a significant upregulation of collagen III and elastin protein expression. These fibrotic changes were prevented by ADSC treatment. less thanbrgreater than less thanbrgreater thanConclusions: This study is the first to test stem cell therapy in an animal model of PD. Injection of ADSCs into the TA during the active phase of PD prevents the formation of fibrosis and elastosis in the TA and corpus cavernosum.

Nyckelord

Antifibrotic
Collagen III
Elastin
Immunohistochemistry
Mesenchymal stromal cells
Polymerase chain reaction
Stem cells
Tunica albuginea
Transforming growth factor beta
Western blot

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