Alterations in platelet aggregation and microsomal benzo‐α‐pyrene hydroxylase activities after exposure of rats to a prudhoe bay crude oil

Abstract Administration of a Prudhoe Bay crude oil (PBCO) to rats has been shown to (a) inhibit platelet aggregation induced by adenosine diphosphate (ADP), arachidonic acid, or epinephrine and (b) induce benzo‐α‐pyrene hydroxylase (BPH) in the liver and small intestine. Maximum inhibition of aggreg...

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Published in:Journal of Biochemical Toxicology
Main Authors: Chaudhury, Shibani, Martin, Marie, Payne, Jeremiah F., Rahimtula, Anver
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1987
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Online Access:http://dx.doi.org/10.1002/jbt.2570020203
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spelling crwiley:10.1002/jbt.2570020203 2024-06-02T08:13:33+00:00 Alterations in platelet aggregation and microsomal benzo‐α‐pyrene hydroxylase activities after exposure of rats to a prudhoe bay crude oil Chaudhury, Shibani Martin, Marie Payne, Jeremiah F. Rahimtula, Anver 1987 http://dx.doi.org/10.1002/jbt.2570020203 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fjbt.2570020203 https://onlinelibrary.wiley.com/doi/pdf/10.1002/jbt.2570020203 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Journal of Biochemical Toxicology volume 2, issue 2, page 93-104 ISSN 0887-2082 1522-7146 journal-article 1987 crwiley https://doi.org/10.1002/jbt.2570020203 2024-05-03T11:21:43Z Abstract Administration of a Prudhoe Bay crude oil (PBCO) to rats has been shown to (a) inhibit platelet aggregation induced by adenosine diphosphate (ADP), arachidonic acid, or epinephrine and (b) induce benzo‐α‐pyrene hydroxylase (BPH) in the liver and small intestine. Maximum inhibition of aggregation (90%) was seen 12 to 16 hours subsequent to dosing. However, substantial inhibition was observed as early as four hours and as late as 48 hours after dosing. Of particular interest was the sensitivity of the platelet response compared with the putatively sensitive response of monooxygenase induction in liver. As little as 0.1 ml of PBCO per kilogram body weight (bw) caused an inhibition of aggregation with all three agonists. A similar inhibition of the release of ADP from platelets in the presence of arachidonic acid or epinephrine was also observed. In contrast, hepatic BPH activity showed only a modest increase (67%) over the control value even after administration of 2 ml of PBCO per kilogram body weight. Small intestine BPH activity was more sensitive, showing a gradual increase of up to 19‐fold 24 hours after dosing with 2 ml of PBCO per kilogram body weight. The sensitivity of the platelet response is of general environmental interest and evaluating platelet aggregation in humans may be important as a noninvasive assay for exposure to either accidental or “acceptable” levels of petroleum hydrocarbons in the occupational environment. Article in Journal/Newspaper Prudhoe Bay Wiley Online Library Journal of Biochemical Toxicology 2 2 93 104
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op_collection_id crwiley
language English
description Abstract Administration of a Prudhoe Bay crude oil (PBCO) to rats has been shown to (a) inhibit platelet aggregation induced by adenosine diphosphate (ADP), arachidonic acid, or epinephrine and (b) induce benzo‐α‐pyrene hydroxylase (BPH) in the liver and small intestine. Maximum inhibition of aggregation (90%) was seen 12 to 16 hours subsequent to dosing. However, substantial inhibition was observed as early as four hours and as late as 48 hours after dosing. Of particular interest was the sensitivity of the platelet response compared with the putatively sensitive response of monooxygenase induction in liver. As little as 0.1 ml of PBCO per kilogram body weight (bw) caused an inhibition of aggregation with all three agonists. A similar inhibition of the release of ADP from platelets in the presence of arachidonic acid or epinephrine was also observed. In contrast, hepatic BPH activity showed only a modest increase (67%) over the control value even after administration of 2 ml of PBCO per kilogram body weight. Small intestine BPH activity was more sensitive, showing a gradual increase of up to 19‐fold 24 hours after dosing with 2 ml of PBCO per kilogram body weight. The sensitivity of the platelet response is of general environmental interest and evaluating platelet aggregation in humans may be important as a noninvasive assay for exposure to either accidental or “acceptable” levels of petroleum hydrocarbons in the occupational environment.
format Article in Journal/Newspaper
author Chaudhury, Shibani
Martin, Marie
Payne, Jeremiah F.
Rahimtula, Anver
spellingShingle Chaudhury, Shibani
Martin, Marie
Payne, Jeremiah F.
Rahimtula, Anver
Alterations in platelet aggregation and microsomal benzo‐α‐pyrene hydroxylase activities after exposure of rats to a prudhoe bay crude oil
author_facet Chaudhury, Shibani
Martin, Marie
Payne, Jeremiah F.
Rahimtula, Anver
author_sort Chaudhury, Shibani
title Alterations in platelet aggregation and microsomal benzo‐α‐pyrene hydroxylase activities after exposure of rats to a prudhoe bay crude oil
title_short Alterations in platelet aggregation and microsomal benzo‐α‐pyrene hydroxylase activities after exposure of rats to a prudhoe bay crude oil
title_full Alterations in platelet aggregation and microsomal benzo‐α‐pyrene hydroxylase activities after exposure of rats to a prudhoe bay crude oil
title_fullStr Alterations in platelet aggregation and microsomal benzo‐α‐pyrene hydroxylase activities after exposure of rats to a prudhoe bay crude oil
title_full_unstemmed Alterations in platelet aggregation and microsomal benzo‐α‐pyrene hydroxylase activities after exposure of rats to a prudhoe bay crude oil
title_sort alterations in platelet aggregation and microsomal benzo‐α‐pyrene hydroxylase activities after exposure of rats to a prudhoe bay crude oil
publisher Wiley
publishDate 1987
url http://dx.doi.org/10.1002/jbt.2570020203
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fjbt.2570020203
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jbt.2570020203
genre Prudhoe Bay
genre_facet Prudhoe Bay
op_source Journal of Biochemical Toxicology
volume 2, issue 2, page 93-104
ISSN 0887-2082 1522-7146
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1002/jbt.2570020203
container_title Journal of Biochemical Toxicology
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op_container_end_page 104
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