Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0032290 (
aspiration pneumonia
)
2,291
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Saliva plays an essential role in the maintenance of oral health. The oral cavity environment changes during aging mainly due to alterations in the secretion and composition of saliva. In particular, unstimulated basal salivary flow decreases with age. The functional decline of the salivary glands impairs chewing and swallowing abilities and often becomes one of the predispositions for aging-related disorders, including
aspiration pneumonia
. The KEAP1-
NRF2
system plays a central role in the regulation of the oxidative stress response.
NRF2
is a transcription factor that coordinately regulates cytoprotective genes, and KEAP1 is a negative regulator of
NRF2
. Although
NRF2
activation has been suggested to be advantageous for the prevention of aging-related diseases, its role in the course of physiological aging is not well understood. To investigate the impact of
NRF2
activation on salivary gland aging, we compared the submandibular glands of Keap1-knockdown (KD) (Keap1
FA/FA
) mice in which
NRF2
is activated with those of wild-type mice. Young mice did not show any apparent differences between the two genotypes, whereas in old mice, clear differences were observed. Aged wild-type submandibular glands exhibited iron and collagen depositions, immune cell infiltration and increased DNA damage and apoptosis accompanied by elevated oxidative stress, which were all markedly attenuated in Keap1-KD mice, suggesting that
NRF2
activation has antiaging effects on salivary glands. We propose that appropriate activation of
NRF2
is effective for the maintenance of healthy salivary gland conditions and for the prevention of hyposalivation in the elderly.
...
PMID:NRF2 pathway activation by KEAP1 inhibition attenuates the manifestation of aging phenotypes in salivary glands. 3259 Mar 31