Stimulation of Cyclic Adenosine 3,5-Monophosphate Formation in Rabbit Choroid Plexus by Beta-Receptor Agonists and Vasoactive Intestinal Polypeptide

1986 ◽  
pp. 491-495
Author(s):  
M. Lindvall ◽  
A. Gustafson ◽  
P. Hedner ◽  
Ch. Owman
1984 ◽  
Vol 100 (2) ◽  
pp. 249-252 ◽  
Author(s):  
A. F. Dixson ◽  
K. M. Kendrick ◽  
M. A. Blank ◽  
S. R. Bloom

ABSTRACT Plasma levels of vasoactive intestinal polypeptide (VIP) in the corpora cavernosa penis and dorsal penile veins greatly exceeded those measured in the limb or caudal veins during anaesthesia in various mammals (Bennett's wallaby, Barbary sheep, cheetah, puma, sooty mangabey, pigtail macaque and chimpanzee). Tactile stimulation of the penis immediately before or during collection of blood samples resulted in an increase. In the wallaby, VIP levels (mean ± s.e.m.) in blood samples collected from the flaccid penis in the absence of tactile stimulation were very low (0·6 ± 0·5 pmol/l). A 36-fold increase in VIP occurred after manual extension of the flaccid penis (24·8 ± 3·2 pmol/l) or during manually stimulated erections (25· 1 ± 1·7 pmol/l). Electrical stimulation of erection produced no significant increase in VIP levels (2·3±0·9 pmol/l) unless accompanied by tactile stimulation (17·5±1·4 pmol/l). These studies provide the first demonstration that sensory feedback from the penis plays an important role in regulating vasoactive intestinal polypeptidergic activity. Since VIP is a potent vasodilator its release due to tactile stimuli during copulation may play a role in the maintenance of penile erection. J. Endocr. (1984) 100, 249–252


Digestion ◽  
1991 ◽  
Vol 50 (2) ◽  
pp. 61-71 ◽  
Author(s):  
Henrik Harling ◽  
Tina Messell ◽  
Steen Seier Poulsen ◽  
Torben None Rasmussen ◽  
Jens Juul Hoist

1985 ◽  
Vol 249 (2) ◽  
pp. G256-G263 ◽  
Author(s):  
K. G. Morgan ◽  
F. Angel ◽  
P. F. Schmalz ◽  
J. H. Szurszewski

Mechanical and intracellular electrical activity was recorded simultaneously in vitro from smooth muscle of the muscularis mucosae of the canine antrum. The intracellularly recorded membrane potential averaged -51 +/- 1.4 mV (mean +/- SE). Spontaneous electrical activity consisted of spike-shaped potentials that were 20–40 mV in amplitude. The rate of rise of the spike potential was slow (less than 0.2 V/s) and the half-time duration was long (0.5-5.0 s). Phasic contractions were often but not always coupled with spike potentials. Ion substitution studies suggested that the spike potential had a greater dependence on Na+ than on Ca2+. Field stimulation of intramural nerves hyperpolarized the membrane potential and abolished spikes or reduced their amplitude and frequency. These changes were associated with a reduction in tone and phasic contractile activity. The response to stimulation of inhibitory nerves was mimicked by epinephrine, neurotensin, and vasoactive intestinal polypeptide. The resistance to adrenergic blocking agents ruled out the possibility of norepinephrine as the transmitter. The tetrodotoxin sensitivity of the response to neurotensin suggests that neurotensin acts indirectly through the inhibitory nerves. Mimicry between the action of applied vasoactive intestinal polypeptide (VIP) and field stimulation provides support for the hypothesis that VIP may be an inhibitory neurotransmitter. These studies indicate that smooth muscle in the canine gastric muscularis mucosae generates spontaneous electrical and mechanical activity and receives a noncholinergic, nonadrenergic inhibitory innervation.


1991 ◽  
Vol 542 (2) ◽  
pp. 241-247 ◽  
Author(s):  
Christer Nilsson ◽  
Jan Fahrenkrug ◽  
Maria Lindvall-Axelsson ◽  
Christer Owman

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