Literature DB >> 12597428

Differentiating spontaneous from drug-induced vascular injury in the dog.

Frances A S Clemo1, Winston E Evering, Paul W Snyder, Mudher A Albassam.   

Abstract

When vascular injury is observed in dogs used in preclinical toxicology studies, careful evaluation of the lesions is warranted, especially when differentiating drug-induced vascular changes from spontaneous findings, such as idiopathic canine polyarteritis. The clinical signs as well as the nature and distribution of lesions can often be distinguishing, as is the case with vasoactive drugs, including vasodilators and/or positive inotropes (hydralazine, minoxidil, endothelin receptor antagonists, and phosphodiesterase III inhibitors). For most types of vasodilator-induced vascular injury, the lesion is often restricted to coronary arteries, whereas in idiopathic canine polyarteritis, arterial lesions not only involve coronary arteries, but also medium to small arteries of other organs. In addition, the nature of the changes in vessels yields important clues. Medial and adventitial hemorrhage is generally associated with vasodilator-induced arterial lesion, whereas hemorrhage is generally absent in idiopathic polyarteritis. Although idiopathic canine polyarteritis can generally be differentiated from vasoactive-induced vascular injury in dogs, there are increasing incidences of this type of polyarteritis in dogs receiving any 1 of a number of unrelated classes of compounds, suggestive of an exacerbation of the spontaneous disease. Therefore, in order to differentiate drug-induced injury from idiopathic canine polyarteritis, it is critical that examination of the vascular pathology be conducted with good understanding of clinical, pharmacological, and mechanistic data associated with the drug.

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Year:  2003        PMID: 12597428     DOI: 10.1080/01926230390174904

Source DB:  PubMed          Journal:  Toxicol Pathol        ISSN: 0192-6233            Impact factor:   1.902


  7 in total

1.  A bilayer small diameter in vitro vascular model for evaluation of drug induced vascular injury.

Authors:  David M Hoganson; Eric B Finkelstein; Gwen E Owens; James C Hsiao; Kurt Y Eng; Katherine M Kulig; Ernest S Kim; Tatiana Kniazeva; Irina Pomerantseva; Craig M Neville; James R Turk; Bernard Fermini; Jeffrey T Borenstein; Joseph P Vacanti
Journal:  Biomicrofluidics       Date:  2016-10-12       Impact factor: 2.800

2.  Is It Adverse, Nonadverse, Adaptive, or Artifact?

Authors:  Arun R Pandiri; Roy L Kerlin; Peter C Mann; Nancy E Everds; Alok K Sharma; L Peyton Myers; Thomas J Steinbach
Journal:  Toxicol Pathol       Date:  2016-10-23       Impact factor: 1.902

Review 3.  Non-proliferative and Proliferative Lesions of the Cardiovascular System of the Rat and Mouse.

Authors:  Brian R Berridge; Vasanthi Mowat; Hirofumi Nagai; Abraham Nyska; Yoshimasa Okazaki; Peter J Clements; Matthias Rinke; Paul W Snyder; Michael C Boyle; Monique Y Wells
Journal:  J Toxicol Pathol       Date:  2016-07-29       Impact factor: 1.628

4.  Successful drug development despite adverse preclinical findings part 1: processes to address issues and most important findings.

Authors:  Robert A Ettlin; Junji Kuroda; Stephanie Plassmann; David E Prentice
Journal:  J Toxicol Pathol       Date:  2010-12-16       Impact factor: 1.628

5.  Successful drug development despite adverse preclinical findings part 2: examples.

Authors:  Robert A Ettlin; Junji Kuroda; Stephanie Plassmann; Makoto Hayashi; David E Prentice
Journal:  J Toxicol Pathol       Date:  2010-12-16       Impact factor: 1.628

6.  A case of spontaneous purulent granulomatous pericarditis in a beagle.

Authors:  Kyohei Kamio; Yutaka Nakanishi; Kenta Matsue; Minoru Sasaki
Journal:  J Toxicol Pathol       Date:  2017-06-04       Impact factor: 1.628

Review 7.  Spontaneously occurring cardiovascular lesions in commonly used laboratory animals.

Authors:  Eugene Herman; Sandy Eldridge
Journal:  Cardiooncology       Date:  2019-06-03
  7 in total

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