Target Inhibition of IL-1 Receptor Prevents Ifosfamide Induced Hemorrhagic Cystitis in Mice
ABCD PBi
Target Inhibition of IL-1 Receptor Prevents Ifosfamide Induced Hemorrhagic Cystitis in Mice
Autor:
Leite, Caio A.V.G
;
Alencar, Viviane T.L
;
Melo, Davi L.R
;
Mota, José M.S.C
;
Melo, Paulo H
;
Mourão, Lívia T.C
;
Wong, Deysi V.T
;
Magalhães, Pedro J.C
;
Santos, Armênio A
;
Brito, Gerly A.C
;
Lima-Júnior, Roberto C.P
;
Cunha
, Fernando Q
;
Ribeiro, Ronaldo A
Assuntos:
Animals
;
antibodies
;
cystitis
;
Cystitis - chemically induced
;
Cystitis - pathology
;
Cystitis - prevention & control
;
Dose-Response Relationship, Drug
;
Drug Synergism
;
Hemorrhage - chemically induced
;
Hemorrhage - pathology
;
Hemorrhage - prevention & control
;
Ifosfamide - toxicity
;
Infliximab - pharmacology
;
Injections, Intraperitoneal
;
interleukin 1 receptor antagonist protein
;
Interleukin 1 Receptor Antagonist Protein - pharmacology
;
interstitial
;
Male
;
Mice
;
Mice, Inbred C57BL
;
monoclonal
;
Receptors, Interleukin-1 - antagonists & inhibitors
;
tumor necrosis factor-alpha
;
Tumor Necrosis Factor-alpha - antagonists & inhibitors
;
urinary bladder
;
Urinary Bladder - drug effects
;
Urinary Bladder - pathology
;
Urology
É parte de:
The Journal of urology, 2015-12, Vol.194 (6),
p
.1777-1786
Notas:
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Descrição:
Purpose Hemorrhagic cystitis is an important dose limiting side effect of ifosfamide based cancer chemotherapy. Despite chemoprophylaxis inflammation can still be found in cystoscopy guided biopsies. Previous studies confirmed the role of TNF-α and IL-1β. We evaluated the protective effect of the IL-1R antagonist anakinra and the anti-TNF-α antibody infliximab in experimental ifosfamide induced hemorrhagic cystitis. Materials and Methods Hemorrhagic cystitis was induced by an injection of ifosfamide (400 mg/kg intraperitoneally) in Swiss wild-type C57Bl/6, IL-1R–/– , TNFR1–/– or TNFR1/R2–/– mice. Mice were treated 30 minutes before ifosfamide with anakinra (100 mg/kg intraperitoneally), infliximab (5 mg/kg intraperitoneally) or vehicle. Visceral nociception was evaluated after hemorrhagic cystitis induction. At 12 hours the animals were sacrificed. Bladders were harvested to assess bladder wet weight, vascular permeability, macroscopic and microscopic findings, muscle contractility, and for cystometrography. Inflammatory cell infiltration was assessed by myeloperoxidase assay and flow cytometry. Results Anakinra attenuated hemorrhage, edema, neutrophil infiltration, visceral hyperalgesia and bladder dysfunction. IL-1R–/– mice also showed milder hemorrhagic cystitis. Infliximab inhibited bladder edema and visceral hyperalgesia without preventing hemorrhage, bladder dysfunction, neutrophils or accumulation. Additionally, the lack of TNFR1 decreased bladder edema but not cell infiltration whereas concomitant deficiency of TNFR1 and TNFR2 resulted in worse hemorrhagic cystitis. Conclusions Anakinra is effective for preventing experimentally ifosfamide induced hemorrhagic cystitis. It seems that neutrophil and macrophage infiltration in this circumstance depends on IL-1 signaling through IL1R. Possibly TNFR2 has a protective role in hemorrhagic cystitis.
Editor:
United States: Elsevier Inc
Idioma:
Inglês