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Response to comment by Moxon et al.
Author(s) -
Dawn Thompson,
Nicola Morrice,
Louise Grant,
Samantha Le Sommer,
Emma K. Lees,
Nimesh Mody,
Heather M. Wilson,
Mirela Delibegović
Publication year - 2018
Publication title -
clinical science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.91
H-Index - 138
eISSN - 1470-8736
pISSN - 0143-5221
DOI - 10.1042/cs20171555
Subject(s) - oil red o , insulin resistance , medicine , cholesterol , apolipoprotein e , in vivo , triglyceride , apolipoprotein b , aorta , endocrinology , obesity , pathology , biology , adipose tissue , genetics , disease , adipogenesis
We would like to thank Clinical Science for the opportunity to respond to the letter [1] which suggests that while we have been able to show that PTP1B inhibitor, trodusquemine, decreases atherosclerotic plaque size as well as serum triglycerides and cholesterol, that we have not shown that it reverses the plaque size, using in vivo imaging techniques such as MRI scanning or ultrasound.Both Ldrl−/− and ApoE−/− mouse models are historically, very well characterized mouse models of atherosclerosis that rapidly develop atherosclerotic plaques under high-fat/high-cholesterol dietary conditions. However, we wanted to confirm this in our own hands, using the gold-standard technique of sectioning the aorta and staining with Oil Red O over time. We now present …

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