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Intravesical resiniferatoxin decreases spinal c‐fos expression and increases bladder volume to reflex micturition in rats with chronic inflamed urinary bladders
Author(s) -
Dinis Paulo,
Charrua Ana,
Avelino António,
Cruz Francisco
Publication year - 2004
Publication title -
bju international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.773
H-Index - 148
eISSN - 1464-410X
pISSN - 1464-4096
DOI - 10.1111/j.1464-4096.2004.04855.x
Subject(s) - resiniferatoxin , urination , spinal cord , medicine , urinary bladder , reflex , dyssynergia , saline , anesthesia , urinary system , urology , endocrinology , receptor , transient receptor potential channel , psychiatry , trpv1
OBJECTIVE To evaluate the effect of intravesical resiniferatoxin on spinal c ‐ fos expression and bladder volume at reflex micturition in rats with chronic urinary bladder inflammation. MATERIALS AND METHODS Of three groups of female Wistar rats, group 1 received cyclophosphamide (75 mg/kg body weight) intraperitoneally every third day (cyclophosphamide is an antitumoral agent that induces bladder inflammation after urinary excretion of its metabolite, acrolein); group 2 comprised sham‐inflamed rats that received saline instead of cyclophosphamide, and group 3 received cyclophosphamide, as group 1, every third day but plus 10 nmol/L resiniferatoxin intravesically, through a urethral catheter, at 7 days. At 8 days, under urethane anaesthesia, a needle was inserted in the bladder dome and saline infused at 6 mL/h for 2 h. Finally the animals were perfusion‐fixed through the ascending aorta with 4% paraformaldehyde. Transverse sections cut from L6 spinal cord segments were immunoreacted for Fos protein and positive cells in the dorsal horn counted. In a further set of equal groups the bladders were prepared in the same way under urethane anaesthesia and after 30‐min of stabilization, saline was infused at 6 mL/h and the volume evoking reflex micturition determined. RESULTS The mean ( Sd ) number of positive c‐ fos cells per spinal cord section was 85 (21), 42 (9) ( P  = 0.002) and 55 (10) in groups 1 to 3, respectively; the values for group 2 and 3 were similar ( P  = 0.22) and statistically less than that of group 1 ( P  = 0.02). Reflex micturition occurred at, respectively, 0.26 (0.09), 0.49 (0.18) and 0.52 (0.11) mL, being similar in group 2 and 3 ( P  = 0.74) but lower in group 1 ( P  = 0.003). CONCLUSION Intravesical resiniferatoxin decreases c‐fos expression and increases bladder capacity in chronically inflamed rat bladders. These findings suggest that desensitizing the vanilloid receptor type 1 by intravesical resiniferatoxin is relevant to the treatment of pain and voiding frequency in patients with chronic inflammatory bladder conditions.

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