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A rat model established by simulating genetic-environmental interactions recapitulates human Alzheimer's disease pathology.
Lin, Xiaomei; Feng, Tianyuyi; Cui, Erheng; Li, Yunfei; Qin, Zhang; Zhao, Xiaohu.
Afiliación
  • Lin X; Department of Imaging, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai 200000, China.
  • Feng T; Department of Imaging, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai 200000, China.
  • Cui E; Department of Imaging, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai 200000, China.
  • Li Y; Department of Imaging, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai 200000, China.
  • Qin Z; Department of Imaging, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai 200000, China.
  • Zhao X; Department of Imaging, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai 200000, China. Electronic address: xhzhao999@263.net.
Brain Res ; 1822: 148663, 2024 01 01.
Article en En | MEDLINE | ID: mdl-37918702
ABSTRACT

BACKGROUND:

In humans, Alzheimer's disease (AD) is typically sporadic in nature, and its pathology is usually influenced by extensive factors. The study established a rat model based on the genetic-environmental interaction.

METHODS:

A rat model was established by transduction of an adeno-associated virus combined with acrolein treatment. Rats were assigned to the normal control (NC), acrolein group, AAV (-) group, AAV-APP group, and AAV-APP/acrolein group. The success of model construction was verified in multiple ways, including by assessing cognitive function, examining microstructural changes in the brain in vivo, and performing immunohistochemistry. The contribution of genetic (APP mutation) and environmental (acrolein) factors to AD-like phenotypes in the model was explored by factorial analysis.

RESULTS:

1) The AAV-APP/acrolein group showed a decline in cognitive function, as indicated by a reduced gray matter volume in key cognition-related brain areas, lower FA values in the hippocampus and internal olfactory cortex, and Aß deposition in the cortex and hippocampus. 2) The AAV-APP group also showed a decline in cognitive function, although the group exhibited atypical brain atrophy in the gray matter and insignificant Aß deposition. 3) The acrolein group did not show any significant changes in Aß levels, gray matter volume, or cognitive function. 4) The genetic factor (APP mutation) explained 39.74% of the AD-like phenotypes in the model factors, and the environmental factor (acrolein exposure) explained 33.3%.

CONCLUSIONS:

The genetic-environmental interaction rat model exhibited a phenotype that resembled the features of human AD and will be useful for research on AD.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos del Conocimiento / Enfermedad de Alzheimer Límite: Animals / Humans Idioma: En Revista: Brain Res Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos del Conocimiento / Enfermedad de Alzheimer Límite: Animals / Humans Idioma: En Revista: Brain Res Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos