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Functional roles of bladder α1‐adrenoceptors in the activation of single‐unit primary bladder afferent activity in rats
Author(s) -
Aizawa Naoki,
Sugiyama Rino,
Ichihara Koji,
Fujimura Tetsuya,
Fukuhara Hiroshi,
Homma Yukio,
Igawa Yasuhiko
Publication year - 2016
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/bju.13313
Subject(s) - silodosin , cystometry , isovolumetric contraction , urology , medicine , afferent , distension , stimulation , urination , urinary bladder , mirabegron , free nerve ending , overactive bladder , endocrinology , chemistry , blood pressure , urinary system , pathology , prostate , lower urinary tract symptoms , cancer , diastole , alternative medicine
Objectives To clarify the involvement of bladder α1‐adrenoceptors (α1‐ARs) in afferent pathways by investigating the effects of silodosin and BMY7378, selective α1A‐ or α1D‐AR antagonists, respectively, on single‐unit afferent nerve fibre activity (SAA) of the primary bladder afferent nerves and their relationship with bladder microcontractions in rats. Materials and Methods A total of 63 female Sprague–Dawley rats were anaesthetized with urethane. The SAA of Aδ and C fibres generated from the left L6 dorsal roots was determined using electrical stimulation of the left pelvic nerve and bladder distension. After measuring baseline SAA during constant filling cystometry, the procedure was repeated with i.v. (0.3–30 μg/kg) or intravesical (10 μ m ) administration of each antagonist. In separate rats, the bladder was filled with saline until the intravesical pressure reached 30 cmH 2 O, and was kept under isovolumetric conditions, then the recording was performed with i.v.‐administered vehicle and silodosin (0.3 μg/kg). Results A total of Aδ fibres and 33 C fibres were isolated from 63 rats. The SAA of Aδ fibres, but not C fibres, were dose‐dependently decreased after both i.v. and intravesical administrations of each of the antagonists. In the experiments under bladder isovolumetric conditions, silodosin administration significantly decreased the SAA of Aδ fibres, but not C fibres, compared with vehicle administration. There were no significant effects on either the mean basal bladder pressure or microcontractions. Conclusion The present study suggests that both α1A‐ or α1D‐ARs in the rat bladder are involved in the activation of the bladder mechanosensory Aδ fibres during bladder filling, and that this activation may not be related to bladder microcontractions.