Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1991-5-2
|
pubmed:abstractText |
Involvement of chloride-dependent, gamma-aminobutyric acid-(GABA-) like synaptic inhibition in the generation of respiratory rhythm was studied in brainstem-spinal cord preparations isolated from newborn rats. Primary respiratory rhythm is presumably generated within the rostral ventrolateral medulla, the site of Pre-I neurones, the firing of which precedes inspiration. Therefore, we examined the responses of Pre-I and inspiratory neurones to GABA antagonists (picrotoxin and bicuculline), a glycine antagonist (strychnine) and reduced chloride concentration in the perfusate. These antagonists (2-20 microM) and reduction of chloride concentration reversibly blocked the transient inhibition of Pre-I activity that occurred during the inspiratory phase. The rhythmic Pre-I and inspiratory neurone activity remained. Changes in the firing properties of Pre-I and inspiratory neurones in 10 microM bicuculline, 10 microM picrotoxin, 5 microM strychnine or reduction of chloride concentration to 40% of normal were analysed statistically. Burst rate of Pre-I neurones tended to increase during these treatments. Delay time from initiation of Pre-I firing to the peak of C4 motorneurone inspiratory activity tended to decrease except during reduced chloride concentration. Changes in mean intraburst firing frequency of Pre-I neurones were not consistent; increase (32%), no change (38%) or decrease (30%). Burst duration of inspiratory neurones decreased. Intraburst firing frequency of inspiratory neurones tended to increase except in 5 microM strychnine. GABA (0.1 mM) or glycine (0.2 mM) reduced the intraburst firing frequency and burst rate of Pre-I neurones, but did not affect the intraburst firing frequency of inspiratory neurones. The burst duration of inspiratory neurones increased during GABA and glycine treatment.(ABSTRACT TRUNCATED AT 250 WORDS)
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Bicuculline,
http://linkedlifedata.com/resource/pubmed/chemical/Chlorides,
http://linkedlifedata.com/resource/pubmed/chemical/GABA Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Glycine,
http://linkedlifedata.com/resource/pubmed/chemical/Picrotoxin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, GABA-A,
http://linkedlifedata.com/resource/pubmed/chemical/Strychnine,
http://linkedlifedata.com/resource/pubmed/chemical/gamma-Aminobutyric Acid
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0031-6768
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
417
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
425-32
|
pubmed:dateRevised |
2003-11-14
|
pubmed:meshHeading |
pubmed-meshheading:1964212-Animals,
pubmed-meshheading:1964212-Animals, Newborn,
pubmed-meshheading:1964212-Bicuculline,
pubmed-meshheading:1964212-Chlorides,
pubmed-meshheading:1964212-GABA Antagonists,
pubmed-meshheading:1964212-Glycine,
pubmed-meshheading:1964212-Medulla Oblongata,
pubmed-meshheading:1964212-Neurons,
pubmed-meshheading:1964212-Picrotoxin,
pubmed-meshheading:1964212-Rats,
pubmed-meshheading:1964212-Rats, Inbred Strains,
pubmed-meshheading:1964212-Receptors, GABA-A,
pubmed-meshheading:1964212-Respiration,
pubmed-meshheading:1964212-Strychnine,
pubmed-meshheading:1964212-Synapses,
pubmed-meshheading:1964212-gamma-Aminobutyric Acid
|
pubmed:year |
1990
|
pubmed:articleTitle |
Inhibitory synaptic inputs to the respiratory rhythm generator in the medulla isolated from newborn rats.
|
pubmed:affiliation |
Department of Physiology, Showa University School of Medicine, Tokyo, Japan.
|
pubmed:publicationType |
Journal Article
|