Amyloid-beta peptide and phosphorylated tau in the frontopolar cerebral cortex and in the cerebellum of toothed whales: aging vs hypoxia
Author(s) -
Simona Sacchini,
Josué DíazDelgado,
A. Espinosa de los Monteros,
Yania Paz-Sánchez,
Yara Bernaldo de Quirós,
Eva Sierra,
Manuel Arbelo,
P. Herráez,
Antonio Fernández
Publication year - 2020
Publication title -
biology open
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.936
H-Index - 41
ISSN - 2046-6390
DOI - 10.1242/bio.054734
Subject(s) - biology , cerebellum , immunolabeling , cerebral cortex , pathology , cerebellar cortex , amyloid beta , neuroscience , hypoxia (environmental) , immunohistochemistry , anatomy , peptide , medicine , immunology , organic chemistry , oxygen , biochemistry , chemistry
Hypoxia could be a possible risk factor for neurodegenerative alterations in cetaceans' brain. Among toothed whales, the beaked whales are particularly cryptic and routinely dive deeper than 1000 m for about 1 h in order to hunt squids and fishes. Samples of frontal cerebral and cerebellar cortex were collected from nine animals, representing six different species of the suborder Odontoceti. Immunohistochemical analysis employed anti-β-amyloid (Aβ) and anti-neurofibrillary tangle (NFT) antibodies. Six of nine (67%) animals showed positive immunolabeling for Aβ and/or NFT. The most striking findings were intranuclear Aβ immunopositivity in cerebral cortical neurons and NFT immunopositivity in cerebellar Purkinje neurons with granulovacuolar degeneration. Aβ plaques were also observed in one elderly animal. Herein, we present immunohistopathological findings classic of Alzheimer's and other neurodegenerative diseases in humans. Our findings could be linked to hypoxic phenomena, as they were more extensive in beaked whales. Despite their adaptations, cetaceans could be vulnerable to sustained and repetitive brain hypoxia.
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