Abstract
To investigate immunotherapy in non-rodent model of Alzheimer’s disease (AD), 14 rabbits were fed a cholesterol/ copper regimen for 10 weeks (“hypercholesterolemic” or “AD model rabbits”), and 4 rabbits were fed normally (“control rabbits”). Six or 8 weeks after diet initiation, 10 hypercholesterolemic and 4 control rabbits were injected with conjugated Aβ1-42-peptide mixed with Freund’s complete adjuvant and boosted every two weeks with 4 additional doses in Freund’s incomplete adjuvant. Serum antibody titers were measured using an Aβ1-42-specific ELISA from blood. Brain Aβ was analyzed with immunohistochemistry. Anti-Aβ antibodies doubled from approximately 2.6 to 5.2 ng/ml. Even with this relatively low increase in anti-Aβ antibodies, there was a significant reduction in intracellular brain Aβ. Pathology is present in AD model rabbits by 4 weeks after diet initiation. Future studies of immunotherapy should begin earlier in disease progression that is comparable to preclinical AD in humans for greater reduction of brain Aβ.
Keywords: Cholesterol, copper, Aβ, temporal cortex, parietal cortex, frontal cortex, Anti-A antibodies, Alzheimer’s disease, TH2 helper, polysorbate-80, Histopathology
Drug Delivery Letters
Title:Immunotherapy in a Rabbit Model of Alzheimer’s Disease
Volume: 2 Issue: 1
Author(s): Diana S. Woodruff-Pak, Christina Shriver, Alexis Agelan, Joanne M. Manns and Richard Coico
Affiliation:
Keywords: Cholesterol, copper, Aβ, temporal cortex, parietal cortex, frontal cortex, Anti-A antibodies, Alzheimer’s disease, TH2 helper, polysorbate-80, Histopathology
Abstract: To investigate immunotherapy in non-rodent model of Alzheimer’s disease (AD), 14 rabbits were fed a cholesterol/ copper regimen for 10 weeks (“hypercholesterolemic” or “AD model rabbits”), and 4 rabbits were fed normally (“control rabbits”). Six or 8 weeks after diet initiation, 10 hypercholesterolemic and 4 control rabbits were injected with conjugated Aβ1-42-peptide mixed with Freund’s complete adjuvant and boosted every two weeks with 4 additional doses in Freund’s incomplete adjuvant. Serum antibody titers were measured using an Aβ1-42-specific ELISA from blood. Brain Aβ was analyzed with immunohistochemistry. Anti-Aβ antibodies doubled from approximately 2.6 to 5.2 ng/ml. Even with this relatively low increase in anti-Aβ antibodies, there was a significant reduction in intracellular brain Aβ. Pathology is present in AD model rabbits by 4 weeks after diet initiation. Future studies of immunotherapy should begin earlier in disease progression that is comparable to preclinical AD in humans for greater reduction of brain Aβ.
Export Options
About this article
Cite this article as:
S. Woodruff-Pak Diana, Shriver Christina, Agelan Alexis, M. Manns Joanne and Coico Richard, Immunotherapy in a Rabbit Model of Alzheimer’s Disease, Drug Delivery Letters 2012; 2 (1) . https://dx.doi.org/10.2174/2210304x11202010014
DOI https://dx.doi.org/10.2174/2210304x11202010014 |
Print ISSN 2210-3031 |
Publisher Name Bentham Science Publisher |
Online ISSN 2210-304X |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
Related Articles
-
Lipoprotein(a): Current Perspectives
Current Vascular Pharmacology Cryptogenic Liver Diseases: Sailing by Sight from HIV Co-Infection with Hepatitis Viruses to HIV Mono-Infection Through the Pillars of Hercules
Current HIV Research Diet and Metabolic Syndrome: An Overview
Current Vascular Pharmacology Protective Substances Against Zinc-Induced Neuronal Death after Ischemia:Carnosine as a Target for Drug of Vascular Type of Dementia
Recent Patents on CNS Drug Discovery (Discontinued) Therapeutic Potential of Drugs Targeting Pathophysiology of Intracerebral Hemorrhage: From Animal Models to Clinical Applications
Current Pharmaceutical Design Vascular Dysfunction in Aging: Potential Effects of Resveratrol, an Anti- Inflammatory Phytoestrogen
Current Medicinal Chemistry Pulmonary Arterial Hypertension in Connective Tissue Diseases
Current Respiratory Medicine Reviews Compritol<sup>®</sup>888 ATO a Lipid Excipient for Sustained Release of Highly Water Soluble Active: Formulation, Scale-up and IVIVC Study
Current Drug Delivery Possible Role of Vascular Risk Factors in Alzheimer's Disease and Vascular Dementia
Current Pharmaceutical Design Patent Selections
Recent Patents on Biotechnology Renin-Angiotensin-Aldosterone System in Autosomal Dominant Polycystic Kidney Disease
Current Hypertension Reviews Efforts to Understand the Molecular Basis of Hypertension Through Drug:Membrane Interactions
Current Topics in Medicinal Chemistry Pleiotropic Effects of Statin in Therapy in Heart Failure: A Review
Current Vascular Pharmacology Dipeptidyl Peptidase IV Inhibitors: A New Paradigm in Type 2 Diabetes Treatment
Current Drug Targets Membrane Processes and Devices for Separation of Bioactive Peptides
Recent Patents on Biotechnology Foot Injuries Among Hajj Pilgrims with and Without Diabetes Mellitus: Implications for Infection Management
Infectious Disorders - Drug Targets Brachial-Ankle Pulse Wave Velocity in the Measurement of Arterial Stiffness: Recent Evidence and Clinical Applications
Current Hypertension Reviews Alzheimers Disease and Retinal Neurodegeneration
Current Alzheimer Research Coenzyme Q10 Reduction with Statins: Another Pleiotropic Effect
Current Drug Therapy Protease-Activated Receptor-2 Antagonists and Agonists
Current Medicinal Chemistry - Cardiovascular & Hematological Agents