Stranded Dolphins’ Brains Show Common Signs of Alzheimer’s Disease

Summary: Researchers found the brains of three species of stranded dolphins had classic biomarkers associated with human Alzheimer’s disease. The findings add weight to the “sick leader” theory, where a group of healthy dolphins finds themselves in dangerously shallow waters after following a group leader showing signs of confusion.

Source: University of Glasgow

The brains of three species of stranded dolphins show classic markers of human Alzheimer’s disease, according to the most extensive study into dementia in odontocetes (toothed whales).

The new pan-Scotland research, a collaboration between the University of Glasgow, the Universities of St Andrews and Edinburgh and the Moredun Research Institute, studied the brains of 22 odontocetes which had all been stranded in Scottish coastal waters.

The study, which is published in the European Journal of Neuroscience, included five different species—Risso’s dolphins, long-finned pilot whales, white-beaked dolphins, harbor porpoises and bottlenose dolphins—and found that four animals from different dolphin species had some of the brain changes associated with Alzheimer’s disease in humans.

The findings may provide a possible answer to unexplained live-stranding events in some odontocete species. Study authors confirm the results could support the “sick-leader” theory, whereby an otherwise healthy pod of animals find themselves in dangerously shallow waters after following a group leader who may have become confused or lost.

Whales, dolphins and porpoises are regularly stranded around the coasts of the U.K. They are often found stranded in groups, or pods, in shallow waters and sometimes on beaches. While some animals can be moved to safer, deeper waters by teams of experts, other animals are less lucky and perish as a result. The underlying causes of live stranding events are not always clear, and research is ongoing to gain better insights.

For this study researchers examined stranded animals for the presence of the brain pathology that are part of the hallmarks of Alzheimer’s disease, including the formation of amyloid-beta plaques, the accumulation of phospho-tau and gliosis (a change in cell numbers in response to central nervous system damage). The results reveal that the brains of all of the aged animals studied had amyloid-beta plaques.

Three animals in particular—each from a different odontocete species—had amyloid-beta plaques as well as a number of other dementia-related pathologies in their brains, showing that some odontocete species develop Alzheimer’s-like neuropathology. However, the study cannot confirm whether any of the animals would have suffered with the same cognitive deficits associated with clinical Alzheimer’s disease in humans.

Lead researcher, Dr. Mark Dagleish from the University of Glasgow, said, “These are significant findings that show, for the first time, that the brain pathology in stranded odontocetes is similar to the brains of humans affected by clinical Alzheimer’s disease.

This shows a painting of a dolphin
The findings may provide a possible answer to unexplained live-stranding events in some odontocete species. Image is in the public domain

“While it is tempting at this stage to speculate that the presence of these brain lesions in odontocetes indicates that they may also suffer with the cognitive deficits associated with human Alzheimer’s disease, more research must be done to better understand what is happening to these animals.”

Co-author, Professor Frank Gunn-Moore from the University of St Andrews, said, “I have always been interested in answering the question: do only humans get dementia? Our findings answer this question as it shows potential dementia associated pathology is indeed not just seen in human patients. This study is also a great example of both different research institutes, but also different branches of the Life Sciences working together.”

Professor Tara Spires-Jones, University of Edinburgh, said, “We were fascinated to see brain changes in aged dolphins similar to those in human aging and Alzheimer’s disease. Whether these pathological changes contribute to these animals stranding is an interesting and important question for future work.”

All animals in this research were studied after a stranding event. Marine Scotland and Defra fund post-mortem examinations, via the Scottish Marine Animal Stranding Scheme (SMASS), of cetaceans (including odontocetes), pinnipeds and marine turtles that strand and die in Scottish coastal waters.

About this animal neuroscience and Alzheimer’s disease research news

Author: Press Office
Source: University of Glasgow
Contact: Press Office – University of Glasgow
Image: The image is in the public domain

Original Research: Open access.
Alzheimer’s disease‐like neuropathology in three species of oceanic dolphin” by Marissa C. Vacher et al. European Journal of Neuroscience


Abstract

Alzheimer’s disease‐like neuropathology in three species of oceanic dolphin

Alzheimer’s disease (AD) is the most common neurodegenerative disease and the primary cause of disability and dependency among elderly humans worldwide. AD is thought to be a disease unique to humans although several other animals develop some aspects of AD-like pathology. Odontocetes (toothed whales) share traits with humans that suggest they may be susceptible to AD.

The brains of 22 stranded odontocetes of five different species were examined using immunohistochemistry to investigate the presence or absence of neuropathological hallmarks of AD: amyloid-beta plaques, phospho-tau accumulation and gliosis.

Immunohistochemistry revealed that all aged animals accumulated amyloid plaque pathology. In three animals of three different species of odontocete, there was co-occurrence of amyloid-beta plaques, intraneuronal accumulation of hyperphosphorylated tau, neuropil threads and neuritic plaques.

One animal showed well-developed neuropil threads, phospho-tau accumulation and neuritic plaques, but no amyloid plaques. Microglia and astrocytes were present as expected in all brain samples examined, but we observed differences in cell morphology and numbers between individual animals.

The simultaneous occurrence of amyloid-beta plaques and hyperphosphorylated tau pathology in the brains of odontocetes shows that these three species develop AD-like neuropathology spontaneously. The significance of this pathology with respect to the health and, ultimately, death of the animals remains to be determined.

However, it may contribute to the cause(s) of unexplained live-stranding in some odontocete species and supports the ‘sick-leader’ theory whereby healthy conspecifics in a pod mass strand due to high social cohesion.

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