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Combined metabolic activators improve metabolic functions in the animal models of neurodegenerative diseases.
Turkez, Hasan; Altay, Ozlem; Yildirim, Serkan; Li, Xiangyu; Yang, Hong; Bayram, Cemil; Bolat, Ismail; Oner, Sena; Tozlu, Ozlem Ozdemir; Arslan, Mehmet Enes; Arif, Muhammad; Yulug, Burak; Hanoglu, Lutfu; Cankaya, Seyda; Lam, Simon; Velioglu, Halil Aziz; Coskun, Ebru; Idil, Ezgi; Nogaylar, Rahim; Ozsimsek, Ahmet; Hacimuftuoglu, Ahmet; Shoaie, Saeed; Zhang, Cheng; Nielsen, Jens; Borén, Jan; Uhlén, Mathias; Mardinoglu, Adil.
Afiliación
  • Turkez H; Department of Medical Biology, Faculty of Medicine, Atatürk University, Erzurum, Turkey.
  • Altay O; Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden. Electronic address: havva.altay@scilifelab.se.
  • Yildirim S; Department of Pathology, Veterinary Faculty, Ataturk University, Erzurum, Turkey. Electronic address: syildirim@atauni.edu.tr.
  • Li X; Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden. Electronic address: xiangyu.li@scilifelab.se.
  • Yang H; Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden. Electronic address: hong.yang@scilifelab.se.
  • Bayram C; Department of Medical Pharmacology, Faculty of Medicine, Atatürk University, Erzurum, Turkey.
  • Bolat I; Department of Pathology, Veterinary Faculty, Ataturk University, Erzurum, Turkey. Electronic address: ismail.bolat@atauni.edu.tr.
  • Oner S; Department of Molecular Biology and Genetics, Faculty of Science, Erzurum Technical University, Erzurum, Turkey.
  • Tozlu OO; Department of Molecular Biology and Genetics, Faculty of Science, Erzurum Technical University, Erzurum, Turkey. Electronic address: ozlem.ozdemir@erzurum.edu.tr.
  • Arslan ME; Department of Molecular Biology and Genetics, Faculty of Science, Erzurum Technical University, Erzurum, Turkey.
  • Arif M; Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden. Electronic address: muhammad.arif@scilifelab.se.
  • Yulug B; Department of Neurology and Neuroscience, Faculty of Medicine, Alanya Alaaddin Keykubat University, Antalya, Turkey.
  • Hanoglu L; Department of Neurology, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey. Electronic address: lhanoglu@kure.com.tr.
  • Cankaya S; Department of Neurology and Neuroscience, Faculty of Medicine, Alanya Alaaddin Keykubat University, Antalya, Turkey.
  • Lam S; Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom. Electronic address: simon.1.lam@kcl.ac.uk.
  • Velioglu HA; Functional Imaging and Cognitive-Affective Neuroscience Lab, Istanbul Medipol University, Istanbul, Turkey; Department of Women's and Children's Health, Karolinska Institute, Neuroimaging Lab, Stockholm, Sweden.
  • Coskun E; Department of Neurology, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey.
  • Idil E; Department of Neurology and Neuroscience, Faculty of Medicine, Alanya Alaaddin Keykubat University, Antalya, Turkey.
  • Nogaylar R; Department of Neurology and Neuroscience, Faculty of Medicine, Alanya Alaaddin Keykubat University, Antalya, Turkey.
  • Ozsimsek A; Department of Neurology and Neuroscience, Faculty of Medicine, Alanya Alaaddin Keykubat University, Antalya, Turkey. Electronic address: ahmeth@atauni.edu.tr.
  • Hacimuftuoglu A; Department of Medical Pharmacology, Faculty of Medicine, Atatürk University, Erzurum, Turkey.
  • Shoaie S; Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden; Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom. Electronic address: saeed.shoaie@scilifelab.se.
  • Zhang C; Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden; School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, PR China. Electronic address: cheng.zhang@scilifelab.se.
  • Nielsen J; Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden. Electronic address: nielsenj@chalmers.se.
  • Borén J; Department of Molecular and Clinical Medicine, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden. Electronic address: Jan.Boren@wlab.gu.se.
  • Uhlén M; Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden. Electronic address: mathias.uhlen@scilifelab.se.
  • Mardinoglu A; Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden; Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom. Electronic address: adilm@scilifelab.se.
Life Sci ; 314: 121325, 2023 Feb 01.
Article en En | MEDLINE | ID: mdl-36581096
ABSTRACT

BACKGROUND:

Neurodegenerative diseases (NDDs), including Alzheimer's disease (AD) and Parkinson's disease (PD), are associated with metabolic abnormalities. Integrative analysis of human clinical data and animal studies have contributed to a better understanding of the molecular and cellular pathways involved in the progression of NDDs. Previously, we have reported that the combined metabolic activators (CMA), which include the precursors of nicotinamide adenine dinucleotide and glutathione can be utilized to alleviate metabolic disorders by activating mitochondrial metabolism.

METHODS:

We first analysed the brain transcriptomics data from AD patients and controls using a brain-specific genome-scale metabolic model (GEM). Then, we investigated the effect of CMA administration in animal models of AD and PD. We evaluated pathological and immunohistochemical findings of brain and liver tissues. Moreover, PD rats were tested for locomotor activity and apomorphine-induced rotation.

FINDINGS:

Analysis of transcriptomics data with GEM revealed that mitochondrial dysfunction is involved in the underlying molecular pathways of AD. In animal models of AD and PD, we showed significant damage in the high-fat diet groups' brain and liver tissues compared to the chow diet. The histological analyses revealed that hyperemia, degeneration and necrosis in neurons were improved by CMA administration in both AD and PD animal models. These findings were supported by immunohistochemical evidence of decreased immunoreactivity in neurons. In parallel to the improvement in the brain, we also observed dramatic metabolic improvement in the liver tissue. CMA administration also showed a beneficial effect on behavioural functions in PD rats.

INTERPRETATION:

Overall, we showed that CMA administration significantly improved behavioural scores in parallel with the neurohistological outcomes in the AD and PD animal models and is a promising treatment for improving the metabolic parameters and brain functions in NDDs.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Enfermedades Neurodegenerativas / Enfermedad de Alzheimer Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Life Sci Año: 2023 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Enfermedades Neurodegenerativas / Enfermedad de Alzheimer Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Life Sci Año: 2023 Tipo del documento: Article País de afiliación: Turquía