Quantitative data describing the impact of the flavonol rutin on in-vivo blood-glucose and fluid-intake profiles, and survival of human-amylin transgenic mice
Jacqueline F. Aitken,
Kerry M. Loomes,
Isabel Riba-Garcia,
Richard D. Unwin,
Gordana Prijic,
Ashley S. Phillips,
Anthony R.J. Phillips,
Donghai Wu,
Sally D. Poppitt,
Ke Ding,
Perdita E. Barran,
Andrew W. Dowsey,
Garth J.S. Cooper
Affiliations
Jacqueline F. Aitken
School of Biological Sciences, University of Auckland, New Zealand
Kerry M. Loomes
School of Biological Sciences, University of Auckland, New Zealand
Isabel Riba-Garcia
Centre for Advanced Discovery and Experimental Therapeutics, CMFT, Manchester Academic Health Sciences Centre, and Institute of Cardiovascular Sciences, Faculty of Biology, Medicine and Health, University of Manchester, UK
Richard D. Unwin
Centre for Advanced Discovery and Experimental Therapeutics, CMFT, Manchester Academic Health Sciences Centre, and Institute of Cardiovascular Sciences, Faculty of Biology, Medicine and Health, University of Manchester, UK
Gordana Prijic
School of Biological Sciences, University of Auckland, New Zealand
Ashley S. Phillips
Michael Barber Centre for Collaborative Mass Spectrometry, Manchester Institute of Biotechnology, University of Manchester, UK
Anthony R.J. Phillips
School of Biological Sciences, University of Auckland, New Zealand
Donghai Wu
Key Laboratory of Regenerative Biology and Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Guangzhou Institute of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China
Sally D. Poppitt
School of Biological Sciences, University of Auckland, New Zealand
Ke Ding
College of Pharmacy, Jinan University, Guangzhou, China
Perdita E. Barran
Michael Barber Centre for Collaborative Mass Spectrometry, Manchester Institute of Biotechnology, University of Manchester, UK
Andrew W. Dowsey
Centre for Advanced Discovery and Experimental Therapeutics, CMFT, Manchester Academic Health Sciences Centre, and Institute of Cardiovascular Sciences, Faculty of Biology, Medicine and Health, University of Manchester, UK
Garth J.S. Cooper
School of Biological Sciences, University of Auckland, New Zealand
Here we provide data describing the time-course of blood-glucose and fluid-intake profiles of diabetic hemizygous human-amylin (hA) transgenic mice orally treated with rutin, and matched control mice treated with water. We employed “parametric change-point regression analysis” for investigation of differences in time-course profiles between the control and rutin-treatment groups to extract, for each animal, baseline levels of blood glucose and fluid-intake, the change-point time at which blood glucose (diabetes-onset) and fluid-intake (polydipsia-onset) accelerated away from baseline, and the rate of this acceleration. The parametric change-point regression approach applied here allowed a much more accurate determination of the exact time of onset of diabetes than do the standard diagnostic criteria. These data are related to the article entitled “Rutin suppresses human-amylin/hIAPP misfolding and oligomer formation in-vitro, and ameliorates diabetes and its impacts in human-amylin/hIAPP transgenic mice” (J.F. Aitken, K.M. Loomes, I. Riba-Garcia, R.D. Unwin, G. Prijic, A.S. Phillips, A.R.J. Phillips, D. Wu, S.D. Poppitt, K. Ding, P.E. Barran, A.W. Dowsey, G.J.S. Cooper. 2016) [1].