Publication: Hypervitaminosis A in rats. Varying responses due to different forms, doses, and routes of administration
dc.contributor.author | V. Leelaprute | en_US |
dc.contributor.author | V. Boonpucknavig | en_US |
dc.contributor.author | N. Bhamarapravati | en_US |
dc.contributor.author | W. Weerapradist | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-03-22T09:23:06Z | |
dc.date.available | 2018-03-22T09:23:06Z | |
dc.date.issued | 1973-12-01 | en_US |
dc.description.abstract | A study made on rats after excessive vitamin A treatment showed that the mortality, bone lesions, and calcification of organs are related to at least three factors, i.e., forms of vitamin A (vitamin A palmitate or vitamin A alcohol), doses (25,000, 50,000, and 75,000 international units (IU)/rat/day), and routes of administration (intraperitoneal or oral). In rats that received vitamin A palmitate by intraperitoneal route, there was no clinical toxicity, no bone lesion, nor soft tissue calcification, but oral administration of vitamin A palmitate of the same dose produced clinical toxicity with bone lesion and soft tissue calcification. Clinical toxicity, bone damage, and tissue calcification developed in animals that received vitamin A alcohol by both routes. The intraperitoneal administration produced more toxicity and more tissue damage in rats than the oral administration. | en_US |
dc.identifier.citation | Archives of Pathology and Laboratory Medicine. Vol.96, No.1 (1973), 5-9 | en_US |
dc.identifier.issn | 00039985 | en_US |
dc.identifier.other | 2-s2.0-0015833616 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/10129 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0015833616&origin=inward | en_US |
dc.subject | Health Professions | en_US |
dc.subject | Medicine | en_US |
dc.title | Hypervitaminosis A in rats. Varying responses due to different forms, doses, and routes of administration | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0015833616&origin=inward | en_US |