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Gewählte Publikation:

Herbert, MK; Schmidt, RF.
Activation of normal and inflamed fine articular afferent units by serotonin.
Pain. 1992; 50(1):79-88 Doi: 10.1016/0304-3959(92)90115-R [OPEN ACCESS]
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Führende Autor*innen der Med Uni Graz
Herbert Michael K.
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Abstract:
In cats anesthetized with alpha-chloralose, extracellular recordings were made from fine afferent units belonging to the medial articular nerve (MAN) of the knee joint. The excitatory and sensitizing effects on articular afferents of serotonin (5-HT) applied intra-arterially close to the joint were examined. The joints were either normal or an experimental arthritis had been induced some hours before the recording session. Bolus injections of 1.35-135 micrograms 5-HT excited about 43% of group III (CV: 2.5-20 m/sec) and 73% of group IV units (CV: less than 2.5 m/sec) from normal joints. The latency was usually between 10 and 30 sec, and the duration and size of the responses were dose-dependent. Fast group III units (CV: greater than 16 m/sec) and group II units (CV: greater than 20 m/sec) were never excited by 5-HT. Repetitive administration led to pronounced tachyphylaxis of the 5-HT response. Inflammation induced an enhanced sensitivity of group III articular afferent units to close intra-arterial application of 5-HT. In particular the total duration of each response was considerably prolonged (4-10 min against 1-2 min under normal conditions). At the same time the tachyphylaxis seen under normal conditions was greatly reduced. In contrast, group IV articular afferent units did not become sensitized to 5-HT in the course of inflammation. In normal joints 5-HT did not sensitize fine afferent units for movement-induced responses. However, after inflammation, a distinct sensitization to such movements by 5-HT application could be observed both in group III and group IV fiber ranges. The sensitization had a short time course not exceeding 7 min. The tonic component of the movement-induced response was more enhanced than the phasic one. The bolus application of 5-HT led to temporary vasoconstriction of the knee joint vessels. This vasoconstriction was especially pronounced in inflamed joints and impeded the access of subsequently applied substances to the terminal regions of the afferent units under observation. It is concluded that the present results support the notion that 5-HT may participate in the mediation of pain from inflamed tissue such as an arthritic joint by exciting and sensitizing fine afferent units. During inflammation group III units are particularly sensitive to 5-HT and, thus, may carry the bulk of the 5-HT-induced nociceptive messages.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Arthritis - pathology Arthritis - physiopathology
Blood Vessels - drug effects
Cats -
Evoked Potentials -
Female -
Knee Joint - blood supply Knee Joint - innervation
Male -
Neurons, Afferent - drug effects Neurons, Afferent - physiology
Physical Stimulation -
Potassium Chloride - pharmacology
Reference Values -
Serotonin - pharmacology
Vasoconstriction - physiology

Find related publications in this database (Keywords)
SEROTONIN (5-HT)
ARTICULAR AFFERENT
JOINT PAIN
INFLAMMATION
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