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1-adrenoceptor subtypes in the
bladder reflex in anesthetized rats
1 Department of Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, 15261; 2 Department of Neurology, Chiba University Graduate School of Medicine, Chiba, 260 - 8670; and 3 Department of Neurology, Chiba-Higashi National Hospital, Chiba, 260 - 8712, Japan
The contribution of different
subtypes of
1-adrenoceptors in the lumbosacral spinal
cord to the control of the urinary bladder was examined in
urethane-anesthetized rats. Bladder pressure was recorded via a
transurethral catheter under isovolumetric conditions. Drugs were
administered intrathecally at the L6-S1
segmental level of spinal cord. RS-100329 (an
1A-antagonist) in doses of 25, 50, and 100 nmol
significantly decreased bladder-contraction amplitude by 38%, 52%,
and 95%, respectively, whereas (+)-cyclazosin (an
1B-antagonist) significantly decreased
bladder-contraction amplitude (48% reduction) only in a 50-nmol but
not a 100-nmol dose. Fifty nanomoles of RS-100329 and (+)-cyclazosin
increased bladder-contraction frequency by 54% and 44%, respectively.
BMY7378 (an
1D-antagonist), in doses of 25, 50, and 100 nmol, did not change bladder activity. These studies suggest that
reflex-bladder activity is modulated by two types of spinal
1-adrenergic mechanisms: 1)
1A- or
1B-inhibitory control of the
frequency of voiding reflexes presumably mediated by an alteration in
the processing of bladder afferent input and 2)
1A-facilitatory modulation of the descending efferent
limb of the micturition-reflex pathway. Spinal
1D-adrenoceptors do not appear to have a significant
role at either site.
afferents; descending efferents; locus ceruleus
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