Source:http://linkedlifedata.com/resource/pubmed/id/19106489
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2009-5-13
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pubmed:abstractText |
The effects of long-term blockade of prolactin (PRL) action by bromocriptine (BRC) treatment on uterine carcinogenesis and on related ovarian physiology were investigated using a rat uterine cancer model. Ten-week-old cycling female Donryu rats, a high yield strain for uterine corpus tumors (endometrial adenocarcinomas), were treated with N-ethyl-N'-nitro-N-nitrosoguanidine (ENNG), as a tumor initiator, and injected with 1 mg/kg body weight BRC subcutaneously 4 times per week until 14.5 months of age to block the proestrus PRL surge. The study was terminated at 15 months of age, and the results showed that long-term BRC treatment significantly inhibited endometrial adenocarcinoma development in terms of both incidence (34.6% to 13.0% with significant difference at 5%) and multiplicity (0.35 to 0.18 with significant difference at 5%), which indicates the number of adenocarcinomas per animals. While BRC did not affect estrous cyclicity in the treated animals, a significant decline was evident in the serum 17 beta-estradiol (E2) to progesterone (P) ratio (E: P ratio), and the serum E2 level showed a decreased tendency at 15 months of age. While the precise pathway to the inhibitory effect could not be determined; the pathway by which ovarian hormonal imbalance decreases the serum E: P ratio most likely plays a crucial role.
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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/Bromocriptine,
http://linkedlifedata.com/resource/pubmed/chemical/Carcinogens,
http://linkedlifedata.com/resource/pubmed/chemical/ENNG,
http://linkedlifedata.com/resource/pubmed/chemical/Estradiol,
http://linkedlifedata.com/resource/pubmed/chemical/Follicle Stimulating Hormone,
http://linkedlifedata.com/resource/pubmed/chemical/Hormone Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Inhibins,
http://linkedlifedata.com/resource/pubmed/chemical/Luteinizing Hormone,
http://linkedlifedata.com/resource/pubmed/chemical/Methylnitronitrosoguanidine,
http://linkedlifedata.com/resource/pubmed/chemical/Progesterone,
http://linkedlifedata.com/resource/pubmed/chemical/Prolactin
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0916-8818
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
55
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
105-9
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pubmed:meshHeading |
pubmed-meshheading:19106489-Adenocarcinoma,
pubmed-meshheading:19106489-Animals,
pubmed-meshheading:19106489-Bromocriptine,
pubmed-meshheading:19106489-Carcinogens,
pubmed-meshheading:19106489-Endometrial Neoplasms,
pubmed-meshheading:19106489-Estradiol,
pubmed-meshheading:19106489-Female,
pubmed-meshheading:19106489-Follicle Stimulating Hormone,
pubmed-meshheading:19106489-Histocytochemistry,
pubmed-meshheading:19106489-Hormone Antagonists,
pubmed-meshheading:19106489-Inhibins,
pubmed-meshheading:19106489-Luteinizing Hormone,
pubmed-meshheading:19106489-Methylnitronitrosoguanidine,
pubmed-meshheading:19106489-Progesterone,
pubmed-meshheading:19106489-Prolactin,
pubmed-meshheading:19106489-Rats
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pubmed:year |
2009
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pubmed:articleTitle |
Long-term treatment with bromocriptine inhibits endometrial adenocarcinoma development in rats.
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pubmed:affiliation |
Division of Pathology, National Institute of Health Sciences, Tokyo, Japan. midoriy@nihs.go.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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