1999
DOI: 10.1002/(sici)1522-7278(199902)14:1<135::aid-tox17>3.0.co;2-l
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The oral toxicity for mice of the tropical cyanobacteriumCylindrospermopsis raciborskii (Woloszynska)

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Cited by 134 publications
(78 citation statements)
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“…The oral toxicity is about 30 fold less than toxicity by i.p. [106]. CYN has two known derivatives, one of them is toxic, 7-epicylindrospermopsin [1] and the other virtually nontoxic, deoxy-cylindrospermosin [86].…”
Section: Cylindrospermopsinsmentioning
confidence: 89%
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“…The oral toxicity is about 30 fold less than toxicity by i.p. [106]. CYN has two known derivatives, one of them is toxic, 7-epicylindrospermopsin [1] and the other virtually nontoxic, deoxy-cylindrospermosin [86].…”
Section: Cylindrospermopsinsmentioning
confidence: 89%
“…Acute poisoning induces death probably due to heart failure, as suggested by Seawright et al [106]. At toxic concentrations, lesion development is quite minor compared to the speed of clinical evolution.…”
Section: Cylindrospermopsinsmentioning
confidence: 99%
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“…Its main target organs are the liver and kidney [54,55], but its citotoxicity is common to other organs. Cylindrospermopsin has a late and progressive acute toxicity, associated to protein synthesis inhibition [56].…”
Section: Toxicological Profiles Of Cyanotoxinsmentioning
confidence: 99%
“…First report by Terao et al (1994) described a massive necrosis of lymphocytes in the cortical layer of the thymus of male mice given a single intraperitoneal dose of 0.2 mg kg -1 purified CYN [24]. Atrophy in lymphoid tissue of the spleen (follicular lymphocyte loss due to lymphophagocytosis) and thymus (degeneration and necrosis of cortical lymphocytes) has also been observed in orally exposed (4.4-8.3 mg CYN kg -1 ) mice [25]. In other rodent experimental model induction of lymphophagocytosis in the mouse spleen at dosing with the cell-free extract at 0.05 mg CYN kg -1 was shown [26].…”
Section: Discussionmentioning
confidence: 99%