Literature DB >> 8996397

Time-dependent remodeling of the bladder wall in growing rabbits after partial outlet obstruction.

F Pampinella1, M Roelofs, E Castellucci, G Passerini-Glazel, F Pagano, S Sartore.   

Abstract

PURPOSE: We asked whether a urethral constriction gradually developed during growth would give rise to a structural remodeling of the bladder wall distinct from that of the mature rabbits in terms of cellular response.
MATERIALS AND METHODS: We examined the serosa and detrusor muscle in immature rabbits whose urethra was obstructed at 30 days postnatal and studied 7 to 30 days after partial outlet obstruction. Morphometry, bromo-deoxyuridine (BrdU) incorporation, Western blotting and immunocytochemical staining with a panel of monoclonal antibodies specific to selected cytoskeletal, cytocontractile and membrane-related proteins unique to non-muscle and smooth muscle cells (SMC) were used to analyze the effects of obstruction on the differentiation pattern.
RESULTS: In comparison with results in adult obstructed bladders, we have found that in growing rabbits: (1) the cell conversion from fibroblasts to SMC, occurring within the 'extrinsic' region of serosal thickening, takes place earlier; (2) newly formed SMC are localized exclusively to the thickened serosa, and can group in bundles depending on the density of the regional innervation; (3) the peak level of BrdU incorporation is more elevated than in the adult bladder wall; and (4) change in the phenotypic profile of SMC of detrusor muscle is delayed.
CONCLUSION: These data indicate that the basic features of structural remodeling in the two models are similar, though partial outlet obstruction produced in growing animals accelerates the fibroblast conversion to SMC and their spatial, differentiation-specific arrangement in the serosa. The late phenotypic changes in obstructed detrusor muscle correlate with the decline of the DNA synthesis level after an initial burst and strongly suggest that newly formed SMC in the serosa do not derive from pre-existing SMC.

Entities:  

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Year:  1997        PMID: 8996397

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  5 in total

1.  Differential expression of SM22 isoforms in myofibroblasts and smooth muscle cells from rabbit bladder.

Authors:  A Chiavegato; M Roelofs; R Franch; E Castellucci; F Sarinella; S Sartore
Journal:  J Muscle Res Cell Motil       Date:  1999-02       Impact factor: 2.698

2.  Protective action of intravesical oxybutynin on bladder ultrastructure in rabbits with detrusor overactivity.

Authors:  Hamilto Yamamoto; Paulo Roberto Kawano; Karina Tuma Balasteghin; Carlos Roberto Padovani; João Luiz Amaro
Journal:  Int Urogynecol J Pelvic Floor Dysfunct       Date:  2008-10-25

Review 3.  Animal models in urological disease and sexual dysfunction.

Authors:  Gordon McMurray; James H Casey; Alasdair M Naylor
Journal:  Br J Pharmacol       Date:  2006-02       Impact factor: 8.739

4.  Urinary outflow obstruction increases apoptosis and deregulates Bcl-2 and Bax expression in the fetal ovine bladder.

Authors:  Nikesh Thiruchelvam; Peter Nyirady; Donald M Peebles; Christopher H Fry; Peter M Cuckow; Adrian S Woolf
Journal:  Am J Pathol       Date:  2003-04       Impact factor: 4.307

5.  Testosterone-induced benign prostatic hyperplasia rat and dog as facile models to assess drugs targeting lower urinary tract symptoms.

Authors:  Jing Li; Yanxin Tian; Shimeng Guo; Haifeng Gu; Qianting Yuan; Xin Xie
Journal:  PLoS One       Date:  2018-01-19       Impact factor: 3.240

  5 in total

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