Source:http://linkedlifedata.com/resource/pubmed/id/16914168
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
22
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pubmed:dateCreated |
2006-10-23
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pubmed:abstractText |
beta-Adrenoceptors (beta-ARs) mediate important physiological functions in salivary glands. Here we investigated the expression and function of beta-AR subtypes in rabbit submandibular gland (SMG). Both beta(1)- and beta(2)-ARs, but not beta(3)-AR, were strongly expressed in rabbit SMG. beta(1)-AR proteins were widely expressed in acinar and ductal cells whereas beta(2)-AR proteins were mainly detected in ductal cells. A [(3)H]-dihydroalprenolol binding assay revealed that beta-AR B(max) was 186+/-11.9 fmol/mg protein and K(d) was 2.71+/-0.23 nM. A competitive binding assay with CGP 20712A, a beta(1)-AR antagonist, indicated that the proportion of beta(1)-AR and beta(2)-AR was 71.9% and 28.1%, respectively. Gland perfusion with the beta-AR agonist isoproterenol induced a significant increase in saliva secretion which was abolished by pretreatment with the non-selective beta-AR antagonist propranolol. Pretreatment with beta(1)- or beta(2)-AR selective antagonists, CGP 20712A or ICI 118551, diminished isoproterenol-induced increase in saliva secretion by 71.2% and 28.8%, respectively. The expression of alpha-amylase mRNA was significantly stimulated by isoproterenol, which was eliminated by propranolol and CGP 20712A. Perfusion with isoproterenol decreased alpha-amylase protein storage in SMG and increased alpha-amylase activity in saliva. These alterations became less significant after pretreatment with propranolol and CGP 20712A. Our results suggest that both beta(1)- and beta(2)-ARs are expressed in rabbit SMG. beta(1)-AR is the predominant subtype and may play an important role in regulating saliva and alpha-amylase secretion.
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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/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/Isoproterenol,
http://linkedlifedata.com/resource/pubmed/chemical/Propranolol,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Adrenergic, beta,
http://linkedlifedata.com/resource/pubmed/chemical/alpha-Amylases
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0024-3205
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
26
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pubmed:volume |
79
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2091-8
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:16914168-Animals,
pubmed-meshheading:16914168-DNA Primers,
pubmed-meshheading:16914168-Isoproterenol,
pubmed-meshheading:16914168-Kinetics,
pubmed-meshheading:16914168-Male,
pubmed-meshheading:16914168-Propranolol,
pubmed-meshheading:16914168-RNA, Messenger,
pubmed-meshheading:16914168-Rabbits,
pubmed-meshheading:16914168-Radioligand Assay,
pubmed-meshheading:16914168-Receptors, Adrenergic, beta,
pubmed-meshheading:16914168-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:16914168-Submandibular Gland,
pubmed-meshheading:16914168-alpha-Amylases
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pubmed:year |
2006
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pubmed:articleTitle |
Expression and functional analysis of beta-adrenoceptor subtypes in rabbit submandibular gland.
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pubmed:affiliation |
Department of Physiology and Pathophysiology, Peking University Health Science Center, Beijing 100083, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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