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H Sann

Publications and source records attributed to H Sann.

At least 73 records · Page 4Linked to original sources
PubMed1992

An opioid peptide inhibits capsaicin-sensitive vasodilatation in the pig's skin.

Microcirculatory effects of electrical stimulation of nerves through a pair of needle electrodes in the skin of anaesthetized pigs were studied by using the laser Doppler flowmetric method. Electrical stimulation (0.3-30 Hz) evoked a short-lasting decrease in capillary blood flux (vasoconstriction) followed by an increase (vasodilatation), of longer duration. Vasoconstriction was inhibited by local guanethidine, but not by capsaicin pretreatment, whereas vasodilatation was blocked by local capsaicin, but not by guanethidine. Both phases of the response were suppressed by local application of tetrodotoxin. Thus, vasoconstriction due to electrical stimulation seems to be of sympathetic origin, while vasodilatation is a result of a release of vasoactive substances from capsaicin-sensitive nerve endings. Vasodilatation due to electrical stimulation was strongly and dose-dependently inhibited by the opioid peptide [D-Met2,Pro5] enkephalinamide, while vasoconstriction remained apparently unchanged. At both doses of the opioid peptide tested (0.03 and 0.15 mumol/kg i.m.) inhibition of vasodilatation was larger at lower than at higher frequencies of stimulation. Guanethidine pretreatment did not influence the inhibitory action of [D-Met2,Pro5] enkephalinamide. Naloxone (1.5 mumol/kg i.m.) reversed or prevented the inhibitory action of the opioid peptide; naloxone on its own did not influence responses due to 0.3-30 Hz stimulation. [D-Met2,Pro5] enkephalinamide (0.15 mumol/kg i.m.) did not influence basal blood flux in the skin, mean arterial blood pressure, respiratory minute volume or respiratory frequency. It was concluded that stimulation of opioid receptors by [D-Met2,Pro5] enkephalinamide is likely to inhibit stimulation-evoked vasodilatation by reducing the release of vasoactive substances from capsaicin-sensitive afferent neurons, an effect that does not depend on functional integrity of sympathetic nerves. Endogenous opioids probably do not modulate the capsaicin-sensitive vasodilatation.

Animals↗
PubMed1992

Substance P and calcitonin gene-related peptide in the ureter of chicken and guinea-pig: distribution, binding sites and possible functions.

To elucidate the possible functional significance of sensory neuropeptides in visceral organs of mammals and birds the distribution, binding sites and the effects on ureteric peristalsis of substance P and calcitonin gene-related peptide (CGRP) were investigated in the ureter of guinea-pigs and chickens. In the guinea-pig numerous substance P and CGRP-immunoreactive fibres were located in the adventitia, smooth muscle layer, submucosa and occasionally in the epithelium. Varicose peptidergic fibres were often found on blood vessels. Binding sites for substance P were associated with blood vessels and epithelium in the following density order: venules greater than epithelium greater than arterioles. The highest density of CGRP binding sites was detected on the smooth muscle; venules and arterioles expressed moderate binding. The peristalsis frequency of the isolated ureter of the guinea-pig was increased by neurokinin A and substance P, whereas CGRP inhibited ureteric motility. In the chicken the immunoreactivity to substance P and CGRP was less pronounced. Immunoreactive fibres were found in the submucosa close to the epithelium and around ureteric ganglion cells. Correspondingly, substance P binding sites were located in the epithelium and in ureteric ganglia; however, specific CGRP binding was restricted to large blood vessels. In the chicken none of the sensory neuropeptides affected ureteric motility. Only high doses of the sensory neurotoxin capsaicin (greater than 10 microM) repeatedly produced a non-specific inhibitory effect, similar to that found in a capsaicin-desensitized guinea-pig ureter preparation. The data suggest that in the guinea-pig ureter sensory neuropeptides play a modulatory role in the regulation of ureteric motility and might have vascular and epithelial functions. In the chicken, substance P might be involved in the regulation of epithelial function and modulation of ganglionic transmission. The physiological or pathophysiological role of sensory neuropeptides and the efferent functions of afferent fibres appears to be much better developed in the guinea-pig than in the chicken.

Animals↗
PubMed1989

Mechanically evoked responses of afferent fibres innervating the guinea-pig's ureter: an in vitro study.

1. Electrophysiological recordings from ureteric mechanosensitive afferent fibres were performed using an in vitro preparation of the guinea-pig ureter and associated nerves. Single-unit recordings were obtained from small ureteric nerves arising from the inferior mesenteric ganglion, the hypogastric nerve or the pelvic plexus. The fibre composition of these ureteric nerves was also examined by electron microscopy. 2. In two ureteric nerve bundles, which were taken as representative of the maximal and minimal size of nerves used in the electrophysiological recordings, the number of nerve fibres was found to be 417 and 48, respectively. In the bigger nerve 12% of the fibres were small myelinated and the rest unmyelinated. The smaller nerve consisted of unmyelinated fibres only. 3. Electrophysiological recordings were made from sixty-seven mechanosensitive afferent fibres. The conduction velocities (CV) of forty-two of them were determined and all were found to be in the C fibre range (mean CV, 0.4 m/s). Of 119 additional fibres which were not further characterized 112 were C fibres (mean CV, 0.51 m/s) and seven were A delta fibres (mean CV, 3.78 m/s). 4. Mechanosensitive units were classified into two groups according to their ability to respond to contractions of the ureter: (i) U-1 units (9% of all mechanosensitive units) responded to contractions of the ureter and did not show on-going activity or after-discharges to mechanical stimulation. They had low thresholds to intraluminal distension (mean, 8 mmHg) and responded with a short latency to pressure stimuli. (ii) U-2 units (91% of all mechanosensitive units) did not respond to contractions of the ureter, had spontaneous activity between 0 and 2.4 Hz and exhibited after-discharges to mechanical stimuli lasting up to several minutes. They responded after a long latency (greater than 3 s) to distensions in the range of 5-30 mmHg. 5. The level of spontaneous activity and the pressure thresholds of the U-2 units were found to be different depending on whether or not the ureter was perfused intraluminally. Thus U-2 units recorded with intraluminal perfusion had a lower rate of on-going activity and higher threshold to intraluminal distension than U-2 units recorded without intraluminal perfusion. 6. Movement of an intraluminal glass bead under the receptive field of the units evoked strong responses in nine of eleven U-2 units tested as soon as their receptive fields were reached. 7. Our results demonstrate the existence of two classes of mechanosensitive afferent fibres in the guinea-pig ureter.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1988

Afferent innervation of the guinea-pig's ureter.

The electrical activity of 41 mechanosensitive afferent units was recored using an in vitro preparation of the guinea-pig's ureter. The conduction velocities of these fibres were found to be in the C-fibre range. Only 4 of them responded to contractions of the ureter. The activation threshold of the units to intraluminal (i.l.) pressure varied between 3 and 50 mm Hg. It is concluded that some of these afferent fibres might be involved in the signalling of nociceptive events.

Animals↗
PubMed1988

Entropy in 12C

Explore the source record for details and available documents.

Journal Article↗
PubMed1988

Vasoactive intestinal peptide stimulates blood flow and secretion of avian salt glands.

The neuromodulatory role of vasoactive intestinal peptide (VIP) in avian salt gland secretion and blood flow was investigated in conscious saltwater-acclimated Pekin ducks. Glandular blood flow was measured by laser-Doppler flowmetry or the radioactive microspheres technique. Osmolal excretion was closely related to salt gland blood flow during salt loading. At threshold conditions of salt gland secretion, VIP infused intracarotidally induced both osmolal excretion and arteriolar vasodilation dose dependently (30-240 pmol.min-1.kg body wt-1). The VIPergic effect on the secretory process for NaCl was enhanced by simultaneous intracarotid application of acetylcholine (5 nmol.min-1.kg body wt-1), whereas the intrinsic vasodilatory potency of acetylcholine appeared to be nonadditive in coinfusion experiments. Ongoing secretion induced by systemic infusion of hypertonic saline could be suppressed by muscarinic antagonists, with salt gland blood flow being sustained at the reduced level of atropine-resistant vasodilation. Subsequent intracarotid infusion of VIP stimulated glandular blood perfusion and also, to a minor extent, osmolal excretion, suggesting an independent, functional VIP system in efferent salt gland control.

Acclimatization↗