Please use this identifier to cite or link to this item:
|Title:||Amitriptyline attenuates interstitial inflammation and ameliorates the progression of renal fibrosis|
|Authors:||Achar, Eduardo [UNIFESP]|
Maciel, Thiago T. [UNIFESP]
Collares, Carlos F.
Teixeira, Vicente de Paulo Castro [UNIFESP]
Schor, Nestor [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
São Paulo City Univ UNICID
São Paulo Poison Control Ctr
unilateral ureteral obstruction
|Publisher:||Nature Publishing Group|
|Citation:||Kidney International. New York: Nature Publishing Group, v. 75, n. 6, p. 596-604, 2009.|
|Abstract:||Amitriptyline is a pleiotropic tricyclic antidepressant, which has anti-oxidant and anti-inflammatory properties. We tested whether amitriptyline might be useful in the treatment of chronic renal disease using the mouse model of unilateral ureteral obstruction. Amitriptyline caused a significant reduction of interstitial fibrosis, determined by Masson's staining, with minimal myofibroblast formation and macrophage infiltration following ureteral obstruction. Using quantitative PCR we found that this treatment significantly reduced the expression of key molecular markers of progressive tubulointerstitial injury such as osteopontin, MCP-1, ICAM-1, and TGF-beta 1 compared to their level in a saline-treated control group. Sublethal X-irradiation or mycophenolate mofetil, treatments that reduce inflammation, were comparable to amitriptyline in the reduction of interstitial fibrosis and macrophage infiltration. These studies in animals suggest that amitriptyline is worth testing as a therapeutic agent that might preserve renal function by blocking inflammation and renal fibrosis.|
|Appears in Collections:||Em verificação - Geral|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.