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Spontaneous photo‐relaxation of urethral smooth muscle from sheep, pig and rat and its relationship with nitrergic neurotransmission
Author(s) -
Triguero D.,
Costa G.,
Labadía A.,
Jiménez E.,
GarcíaPascual A.
Publication year - 2000
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1111/j.1469-7793.2000.00443.x
Subject(s) - neurotransmission , nitric oxide , chemistry , medicine , endocrinology , urethra , stimulation , nitric oxide synthase , neurotransmitter , adenylyl cyclase , superoxide , soluble guanylyl cyclase , endogeny , urinary system , neuromuscular transmission , guanylate cyclase , biology , anatomy , biochemistry , receptor , enzyme
In the present work we have characterized the relaxant response induced by light stimulation (LS) in the lower urinary tract from sheep, pig and rat, establishing its relationship with nitrergic neurotransmission. Urethral, but not detrusor, preparations showed pronounced photo‐relaxation (PR) which declined progressively following repetitive LS. Sheep urethral PR was again restored either spontaneously or (to a greater extent) by exogenous nitric oxide (NO) addition and by electrical field stimulation (EFS) of intrinsic nitrergic nerves. Greater NO generation was detected from sheep urethral than from detrusor homogenates following illumination. Sheep urethral PR was inhibited by oxyhaemoglobin, but not by methaemoglobin, carboxy‐PTIO, extracellular superoxide anion generators or superoxide dismutase. Guanylyl cyclase but not adenylyl cyclase activation mediates urethral relaxation to LS. Urethral PR was more resistant to inhibition by L‐thiocitrulline than EFS‐induced responses, although this agent prevented PR restoration by high‐frequency EFS. Urethral PR was TTX insensitive and partially modified in high‐K + solutions. Cold storage for 24 h greatly impaired urethral PR, although it was restored by high‐frequency EFS. Repetitive exposure to LS, EFS or exogenous NO induced changes in the shape of the EFS‐induced nitrergic relaxation, possibly by pre‐synaptic mechanisms. In conclusion, we suggest the presence of an endogenous, photo‐labile, nitro‐compound store in the urethra, which seems to be replenished by neural nitric oxide synthase activity, indicating a close functional relationship with the nitrergic neurotransmitter.