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Enhanced Anti-Amyloid Effect of Combined Leptin and Pioglitazone in APP/PS1 Transgenic Mice.
Liu, Yao; Hanson, Kelsey A; McCormack, Graeme; Atkinson, Rachel A K; Dittmann, Justin; Vickers, James C; Fernandez-Martos, Carmen M; King, Anna E.
Afiliação
  • Liu Y; Wicking Dementia Research and Education Centre, College of Health and Medicine, University of Tasmania, Private Bag 143, Hobart, Tasmania 7001, Australia.
  • Hanson KA; Division of Neuroscience & Experimental Psychology, University of Manchester, 46 Grafton Street, Manchester, M13 9NT, United Kingdom.
  • McCormack G; Wicking Dementia Research and Education Centre, College of Health and Medicine, University of Tasmania, Private Bag 143, Hobart, Tasmania 7001, Australia.
  • Atkinson RAK; Wicking Dementia Research and Education Centre, College of Health and Medicine, University of Tasmania, Private Bag 143, Hobart, Tasmania 7001, Australia.
  • Dittmann J; Wicking Dementia Research and Education Centre, College of Health and Medicine, University of Tasmania, Private Bag 143, Hobart, Tasmania 7001, Australia.
  • Vickers JC; Wicking Dementia Research and Education Centre, College of Health and Medicine, University of Tasmania, Private Bag 143, Hobart, Tasmania 7001, Australia.
  • Fernandez-Martos CM; Research Unit of the National Hospital of Paraplegics (UDI-HNP), Finca La Peraleda s/n, Toledo 45007, Spain.
  • King AE; Wicking Dementia Research and Education Centre, College of Health and Medicine, University of Tasmania, Private Bag 143, Hobart, Tasmania 7001, Australia.
Curr Alzheimer Res ; 17(14): 1294-1301, 2020.
Article em En | MEDLINE | ID: mdl-33602093
ABSTRACT

BACKGROUND:

Alzheimer's disease (AD) has challenged single-target therapeutic strategies, raising the possibility that combined therapies may offer a more effective treatment strategy.

OBJECTIVE:

There is substantial evidence for the efficacy of leptin (L) (neuroprotective hormone) and pioglitazone (P) (anti-inflammatory agent) as monotherapies in AD. We have previously shown that combination treatment of L+P in APP/PS1 mice at the onset of pathology significantly improved memory and reduced brain Aß levels relative to control mice. In this new study, we sought to replicate our previous findings in a new cohort of APP/PS1 mice to further confirm whether the combined treatment of L+P is superior to each treatment individually.

METHODS:

We have re-evaluated the effects of L+P co-treatment in APP/PS1 mice using thioflavin-S staining, MOAß immunolabeling, and enzyme-linked immunosorbent assay (ELISA) to examine effects on Aß levels and pathology, relative to animals that received L or P individually.

RESULTS:

We demonstrated that a combination of L and P significantly enhances the anti-Aß effect of L or P in the hippocampus of APP/PS1 mice.

CONCLUSION:

Our findings suggest that combining L and P significantly enhances the anti-Aß effect of L or P in the hippocampus of APP/PS1 mice and maybe a potential new effective strategy for AD therapy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Camundongos Transgênicos / Peptídeos beta-Amiloides / Leptina / Pioglitazona / Hipocampo / Hipoglicemiantes Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Camundongos Transgênicos / Peptídeos beta-Amiloides / Leptina / Pioglitazona / Hipocampo / Hipoglicemiantes Idioma: En Ano de publicação: 2020 Tipo de documento: Article