Medizinische Universität Graz - Research portal

Go directly to the nagivation.
Go directly to the content.

Navigation/Search

Selected Publication:

Lembeck, F; Donnerer, J.
Postocclusive cutaneous vasodilatation mediated by substance P.
Naunyn Schmiedebergs Arch Pharmacol. 1981; 316(2):165-171 Doi: 10.1007/BF00505312
Web of Science PubMed FullText FullText_MUG Google Scholar

Leading authors Med Uni Graz: Lembeck Fred
Co-authors Med Uni Graz: Donnerer Josef
Altmetrics:
Dimensions Citations:
Plum Analytics:
Scite (citation analytics):
Abstract:: 1. The cutaneous vasodilatation following arterial occlusion ("reactive hyperemia") was studied in the rat hind paw. A peak increase in venous outflow of 200-250% was observed within 1 min after a 3 min occlusion period. 2. Chronic denervation as well as capsaicin pretreatment reduced the postocclusive cutaneous vasodilatation by more than 60% (P less than 0.01). This demonstrates that the reactive vasodilatation is of neurogenic origin and mediated by small diameter afferent fibres. 3. Reduction of the postocclusive cutaneous vasodilatation after histamine depletion by compound 48/80 indicates the involvement of histamine. 4. Among all neuropeptides known to occur in primary sensory neurones only substance P and vasoactive intestinal polypeptide cause vasodilatation when infused i.a. into the rat paw. In contrast to antidromic sensory nerve stimulation or i.a. substance P infusion, vasoactive intestinal polypeptide does not cause plasma extravasation. The vasodilator potency of vasoactive intestinal polypeptide is about 1/500 of substance P in the rat paw. Therefore only substance P is able to mimic the reactive vasodilatation. 5. It is concluded that the postocclusive cutaneous vasodilatation is caused mainly by the release of substance P from peripheral endings of small diameter nerve fibres. The "axon reflex", also involving neurogenic vasodilatation, is assumed to be exerted by the same mechanism.
Find related publications in this database (using NLM MeSH Indexing): Animals -; Arterial Occlusive Diseases - physiopathology; Axons - physiology; Histamine Release - physiology; Male - physiology; Neurotransmitter Agents - secretion; Peripheral Nerves - secretion; Rats - secretion; Reflex - secretion; Skin - blood supply; Substance P - pharmacology; Vasoactive Intestinal Peptide - pharmacology; Vasodilation - drug effects