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1.
Pain ; 123(1-2): 127-36, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16707223

ABSTRACT

Noxious stimuli that are applied to different somatic sites interact; often one stimulus diminishes the sensation elicited from another site. By contrast, inhibitory interactions between visceral stimuli are not well documented. We investigated the interaction between the effects of noxious distension of the colorectum and noxious stimuli applied to the jejunum, in the rat. Colorectal distension elicited a visceromotor reflex, which was quantified using electromyographic (EMG) recordings from the external oblique muscle of the upper abdomen. The same motor units were activated when a strong pinch was applied to the flank skin. Distension of the jejunum did not provoke an EMG response at this site, but when it was applied during colorectal distension it blocked the EMG response. Jejunal distension also inhibited the response to noxious skin pinch. The inhibition of the visceromotor response to colorectal distension was prevented by local application of tetrodotoxin to the jejunum, and was markedly reduced when nicardipine was infused into the local jejunal circulation. Chronic sub-diaphragmatic vagotomy had no effect on the colorectal distension-induced EMG activity or its inhibition by jejunal distension. The nicotinic antagonist hexamethonium suppressed phasic contractile activity in the jejunum, had only a small effect on the inhibition of visceromotor response by jejunal distension. It is concluded that signals that arise from skin pinch and colorectal distension converge in the central nervous system with pathways that are activated by jejunal spinal afferents; the jejunal signals strongly inhibit the abdominal motor activity evoked by noxious stimuli.


Subject(s)
Abdominal Muscles/physiopathology , Afferent Pathways/physiopathology , Colon/innervation , Jejunum/innervation , Pain/physiopathology , Pressure/adverse effects , Rectum/innervation , Skin/innervation , Analgesia , Animals , Calcium Channel Blockers/pharmacology , Calcium Channels, L-Type/drug effects , Catheterization , Dilatation, Pathologic/physiopathology , Electromyography , Hexamethonium/pharmacology , Male , Nicardipine/pharmacology , Nicotinic Antagonists/pharmacology , Nociceptors/physiology , Rats , Rats, Sprague-Dawley , Sodium Channel Blockers/pharmacology , Spinal Cord/physiopathology , Tetrodotoxin/pharmacology , Transducers, Pressure , Vagotomy
2.
Spine (Phila Pa 1976) ; 29(2): 129-38, 2004 Jan 15.
Article in English | MEDLINE | ID: mdl-14722403

ABSTRACT

STUDY DESIGN: Traction was applied to muscles attaching to the posterior and middle layers of lumbar fascia (PLF, MLF). Effects on fasciae were determined via tensile force measures and movement of markers. OBJECTIVES: To document tensile transmission to the PLF and MLF when traction was applied to latissimus dorsi (LD), gluteus maximus (GM), external and internal oblique (EO, IO), and transversus abdominis (TrA) in unembalmed cadavers. SUMMARY OF BACKGROUND DATA: A previous study on embalmed cadavers applied traction to muscle attachments while monitoring fascial movement but did not test TrA or the MLF. METHODS: The PLF and MLF were dissected then marked on eight unembalmed cadavers. A strain gauge was inserted through fascia at L3; 10N traction was applied to each muscle attachment while photographs and tension measures were taken. Movement of fascial markers was detected photographically. Fascial widths were also measured. RESULTS: Tension was clearly transmitted to fascial vertebral attachments. Tensile forces and fascial areas affected were highest for traction on LD and TrA in the PLF and for TrA in the MLF. Movement of PLF markers from tension on LD and TrA occurred bilaterally between T12 and S1. Effects from other muscles were variably bilateral, with those from GM and IO occurring below L3 and those from EO occurring above L3. Tensile forces were relatively high in the MLF and its width was less than half that of the PLF. CONCLUSIONS: Low levels of tension are effectively transmitted between TrA and the MLF or PLF. Via them, TrA may influence intersegmental movement.


Subject(s)
Cadaver , Fascia/physiopathology , Muscle, Skeletal/physiopathology , Aged , Aged, 80 and over , Biomechanical Phenomena , Dissection , Fascia/pathology , Female , Humans , Lumbosacral Region , Male , Stress, Mechanical
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