1992
DOI: 10.1111/j.1600-0773.1992.tb00426.x
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Intestinal Absorption of Inorganic Mercury in Rat

Abstract: 203Hg-Mercuric chloride was administered intragastrically to female rats. The absorption rate evaluated for a broad range of doses was found constant for low and medium range, and higher for high doses. Mercury was determined in internal organs and intestines. The time-course of intestinal mercury indicated that a deposit formed initially in the mucosa was further absorbed into the circulation. No indication was found of a protection mechanism based on exfoliation of the mucosal deposits of metal.

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Cited by 17 publications
(9 citation statements)
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“…After ingestion, a slight amount of methylmercury is converted by intestine germs to inorganic form (Nakamura et al, 1977;Rowland et al, 1980) which is not as well bioavailable as the organic form (Clarkson, 1971;Kostial et al, 1978;Piotrowski et al, 1992;) and the majority of methylmercury is distributed ubiquitously in all tissues Data are mean ± SD. NS, not significant.…”
Section: Discussionmentioning
confidence: 99%
“…After ingestion, a slight amount of methylmercury is converted by intestine germs to inorganic form (Nakamura et al, 1977;Rowland et al, 1980) which is not as well bioavailable as the organic form (Clarkson, 1971;Kostial et al, 1978;Piotrowski et al, 1992;) and the majority of methylmercury is distributed ubiquitously in all tissues Data are mean ± SD. NS, not significant.…”
Section: Discussionmentioning
confidence: 99%
“…Published values for the absolute bioavailability of mercuric chloride in adult animals range from 1-25% (Kostial et al, 1978;Piotrowski et al, 1992;Nielsen and Andersen, 1990). If more reports of the bioavailability of other forms of mercury become available, they too are likely to vary.…”
Section: Better Characterization Of the Variation In Absolute Bioavaimentioning
confidence: 97%
“…@ and at higher doses compared to low doses. (32) In adult mice, "true absorption" of mercuric chloride (determined by comparing the whole-body retention at 3-14 days following oral vs. intraperitoneal administration of a single dose) was estimated to be 20-25% (range 17-30%). '24)…”
Section: In Vivo Estimates Of the Bioavailability Of Inorganic Mercurmentioning
confidence: 99%