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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1994-12-20
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pubmed:abstractText |
The concentration of acetylcholine (ACh) in rat jejunum that had been homogenized with an ultra-high-speed homogenizer (Biotron) was significantly higher than that in jejunum homogenized with a glass homogenizer. Rats were injected once or repeatedly for 10 days with a muscarinic agonist, pilocarpine (1 mg/kg), or a muscarinic antagonist, scopolamine (5 mg/kg). Animals were killed 20 min or 24 hr after single or consecutive injections, respectively, for determinations of cholinergic activities in the jejunum. Single treatment: Pilocarpine did not cause significant changes in the level of ACh, the activity of acetylcholinesterase (AChE), the binding of [3H]quinuclidinyl benzilate (QNB) or the contractile responses to ACh. Scopolamine reduced the level of ACh and binding of [3H]QNB without inducing significant changes in the activity of AChE and the contractile response. Consecutive treatment: Pilocarpine reduced the binding of [3H]QNB by changing the value of Bmax and reduced the contractile response without affecting the level of ACh or the activity of AChE. Scopolamine increased the binding of [3H]QNB without any effects on the level of ACh, the activity of AChE or the contractile response. In summary, it is possible to determine the level of ACh in a tissue as hard as intestine by homogenization with a Biotron and to assess the cholinergic situation in the intestine of animals that have been poisoned with various agents by estimating cholinergic activities.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acetylcholine,
http://linkedlifedata.com/resource/pubmed/chemical/Acetylcholinesterase,
http://linkedlifedata.com/resource/pubmed/chemical/Pilocarpine,
http://linkedlifedata.com/resource/pubmed/chemical/Quinuclidinyl Benzilate,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Muscarinic,
http://linkedlifedata.com/resource/pubmed/chemical/Scopolamine Hydrobromide
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0388-1350
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
133-40
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:7966450-Acetylcholine,
pubmed-meshheading:7966450-Acetylcholinesterase,
pubmed-meshheading:7966450-Animals,
pubmed-meshheading:7966450-Cell Fractionation,
pubmed-meshheading:7966450-Jejunum,
pubmed-meshheading:7966450-Male,
pubmed-meshheading:7966450-Pilocarpine,
pubmed-meshheading:7966450-Quinuclidinyl Benzilate,
pubmed-meshheading:7966450-Rats,
pubmed-meshheading:7966450-Rats, Wistar,
pubmed-meshheading:7966450-Receptors, Muscarinic,
pubmed-meshheading:7966450-Scopolamine Hydrobromide
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pubmed:year |
1994
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pubmed:articleTitle |
Complementary improvement of the method for determining cholinergic activities in the small intestine and its application to experiments in vivo.
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pubmed:affiliation |
Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Japan.
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pubmed:publicationType |
Journal Article,
Comparative Study
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