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고프로락틴 혈증 환자에서 중추신경계의 도파민 분비장애

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dc.contributor.author이현철-
dc.date.accessioned2021-09-28T08:13:55Z-
dc.date.available2021-09-28T08:13:55Z-
dc.date.issued1996-09-
dc.identifier.issn1015-6380-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/183510-
dc.description.abstractBackground: Prolactin(PRL) secretion is tonically inhibited by doparnine that originates from the hypothalamic tuberoinfundibular tract and reaches the lactotroph via the hypophyseal portal vessel. Hyperprolactinemia associated with oligomenorrhea-amenorrhea, galactorrhea and/or infertility is mainly due to PRL-secreting pituitary adenoma(PA). The diagnosis of idiopathic hyperprolac- tinemia(IHP) is made, when hyperprolactinemia is sustained and all causes of hyperprolactinemia are excluded without radiological abnormality. It is not known, whether IHP and PA are two distinct entities or two subsequent phases of the same disease. The etiology of both disorders remains unresolved. We investigated that PRL hypersecretion in patients with IHP and PA may be the result of a defect in the central nervous system(CNS)-dopamine release, and that there may be some differences in pathogenesis of both diseases. Methods: We measured 24 hour-urinary dopamine, norepinephrine, epinephrine, and serum and 24 hour-urinary VMA(vanillyl rnandelic acid), HVA(homovanilic acid), DOPAC(3,4-dihydroxy phenylaceticacid), MHPG(3-methoxy 4-hydroxy phenylglycol) in 10 normal controls, 9 patients with IHP, and 17 patients with PA in the early follicular phase. Results: Urinary HVA and DOPAC concentrations, the major metabolites of CNS dopaminergic activity, were signficantly lower in both patients with IHP and PA compared with those in normal controls(p 0.05), whereas they were not different in both disease groups. Dopamine, norepine-phrine, epinephrine, MHPG concentrations were similar to those of the normal controls. Although VMA concentrations of both disease groups were significantly higher than those of normal controls, all of them were within normal range. Conelusion: Although our data are unable to establish the precise biochemical defect responsible for central dopamine deficiency in pathogensis of IHP and PA, we can support the presence of a pathological reduction of brain dopamine activity in IHP and PA-
dc.description.statementOfResponsibilityopen-
dc.languageKorean-
dc.publisher대한내분비학회-
dc.relation.isPartOfJournal of Korea Society of Endocrinology(대한내분비학회지)-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.title고프로락틴 혈증 환자에서 중추신경계의 도파민 분비장애-
dc.title.alternativeReduction of Central Dopamine Release in Hyperprolactinemia-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthor차봉수-
dc.contributor.googleauthor송영득-
dc.contributor.googleauthor임승길-
dc.contributor.googleauthor김경래-
dc.contributor.googleauthor이현철-
dc.contributor.googleauthor허갑범-
dc.contributor.googleauthor남수연-
dc.contributor.googleauthor이은직-
dc.contributor.googleauthor정봉철-
dc.contributor.googleauthor김정한-
dc.contributor.googleauthor오세창-
dc.contributor.localIdA03301-
dc.relation.journalcodeJ01478-
dc.subject.keywordProlactinoma-
dc.subject.keywordIdiopathic hyperprolactinemia-
dc.contributor.alternativeNameLee, Hyun Chul-
dc.contributor.affiliatedAuthor이현철-
dc.citation.volume11-
dc.citation.number3-
dc.citation.startPage277-
dc.citation.endPage284-
dc.identifier.bibliographicCitationJournal of Korea Society of Endocrinology (대한내분비학회지), Vol.11(3) : 277-284, 1996-09-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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