Abstract | BACKGROUND: METHODS: 10-day-old male rats received 0.2 mL of 0.1% iodoacetamide in 2% sucrose daily by oral gavages for 6 days. Control group received 2% sucrose. At 8-10 weeks rats treated with baclofen (0.3, 1, and 3 mg kg(-1) bw) or saline were tested for behavioral and electromyographic (EMG) visceromotor responses; gastric spinal afferent nerve activity to graded gastric distention and Fos protein expression in dorsal horn of spinal cord segments T8-T10 to noxious gastric distention. KEY RESULTS:
Baclofen administration was associated with a significant attenuation of the behavioral and EMG responses (at 1 and 3 mg kg(-1)) and expression of Fos in T8 and T9 segments in neonatal iodoacetamide sensitized rats. However, baclofen administration did not significantly affect splanchnic nerve activity to gastric distention. Baclofen (3 mg kg(-1)) also significantly reduced the expression of spinal Fos in response to gastric distention in control rats to a lesser extent than sensitized rats. CONCLUSIONS & INFERENCES:
Baclofen is effective in attenuating pain associated responses in an experimental model of FD and appears to act by central mechanisms. These results provide a basis for clinical trials of this drug in FD patients.
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Authors | L S Liu, M Shenoy, P J Pasricha |
Journal | Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society
(Neurogastroenterol Motil)
Vol. 23
Issue 4
Pg. 356-61, e160-1
(Apr 2011)
ISSN: 1365-2982 [Electronic] England |
PMID | 21199535
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2011 Blackwell Publishing Ltd. |
Chemical References |
- Analgesics
- GABA-A Receptor Agonists
- Proto-Oncogene Proteins c-fos
- Baclofen
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Topics |
- Analgesics
(therapeutic use)
- Animals
- Baclofen
(therapeutic use)
- Disease Models, Animal
- Dyspepsia
(complications, drug therapy, physiopathology)
- Electromyography
- GABA-A Receptor Agonists
(therapeutic use)
- Gastrointestinal Motility
(drug effects, physiology)
- Male
- Pain
(drug therapy, etiology)
- Posterior Horn Cells
(metabolism)
- Proto-Oncogene Proteins c-fos
(metabolism)
- Rats
- Rats, Sprague-Dawley
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