Oral treatment with the all-d-peptide RD2 enhances cognition in aged beagle dogs – A model of sporadic Alzheimer’s disease
Janine Kutzsche,
Sarah Schemmert,
Tuyen Bujnicki,
Christian Zafiu,
Steffen Halbgebauer,
Victoria Kraemer-Schulien,
Marlene Pils,
Lara Blömeke,
Julia Post,
Andreas Kulawik,
Dagmar Jürgens,
Wolfgang M. Rossberg,
Michael Hümpel,
Oliver Bannach,
Markus Otto,
Joseph A. Araujo,
Antje Willuweit,
Dieter Willbold
Affiliations
Janine Kutzsche
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany
Sarah Schemmert
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany
Tuyen Bujnicki
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany
Christian Zafiu
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany
Steffen Halbgebauer
Institute of Experimental Neurology, Ulm University Hospital, Ulm, Germany
Victoria Kraemer-Schulien
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany
Marlene Pils
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany; attyloid GmbH, Düsseldorf, Germany
Lara Blömeke
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany; Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany
Julia Post
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany; Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany
Andreas Kulawik
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany
Dagmar Jürgens
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany
Wolfgang M. Rossberg
ConsultWMR, Potsdam, Germany
Michael Hümpel
KAIROSmetics UG, Berlin, Germany
Oliver Bannach
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany; Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany; attyloid GmbH, Düsseldorf, Germany
Markus Otto
Institute of Experimental Neurology, Ulm University Hospital, Ulm, Germany
Joseph A. Araujo
InterVivo Solutions, Fergus, Canada
Antje Willuweit
Institute of Neuroscience and Medicine, Medical Imaging Physics (INM-4), Forschungszentrum Jülich, Jülich, Germany
Dieter Willbold
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany; Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany; Corresponding author. Forschungszentrum Jülich GmbH Institute of Biological Information Processing, Structural Biochemistry (IBI-7), 52425, Jülich, Germany.
Disease-modifying therapies to treat Alzheimer's disease (AD) are of fundamental interest for aging humans, societies, and health care systems. Predictable disease progression in transgenic AD models favors preclinical studies employing a preventive study design with an early pre-symptomatic treatment start, instead of assessing a truly curative approach with treatment starting after diagnosed disease onset. The aim of this study was to investigate the pharmacokinetic profile and efficacy of RD2 to enhance short-term memory and cognition in cognitively impaired aged Beagle dogs - a non-transgenic model of truly sporadic AD. RD2 has previously demonstrated pharmacodynamic efficacy in three different transgenic AD mouse models in three different laboratories. Here, we demonstrate that oral treatment with RD2 significantly reduced cognitive deficits in cognitively impaired aged Beagle dogs even beyond the treatment end, which suggests in combination with the treatment dependent CSF tau oligomer decrease a disease-modifying effect of RD2 treatment.