Open AccessNicotinate‐curcumin ameliorates cognitive impairment in diabetic rats by rescuing autophagic flux in CA1 hippocampus
Author(s) -
Gu HongFeng,
Li Na,
Tang YaLing,
Yan CanQun,
Shi Zhe,
Yi SiNi,
Zhou HaoLing,
Liao DuanFang,
OuYang XinPing
Publication year - 2019
Publication title -
cns neuroscience and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 69
eISSN - 1755-5949
pISSN - 1755-5930
DOI - 10.1111/cns.13059
Subject(s) - autophagy , curcumin , flux (metallurgy) , streptozotocin , pi3k/akt/mtor pathway , ampk , hippocampus , cognitive decline , chemistry , pharmacology , apoptosis , microbiology and biotechnology , kinase , endocrinology , medicine , protein kinase a , diabetes mellitus , biology , biochemistry , dementia , disease , organic chemistry
Our previous study has confirmed that a novel curcumin derivate nicotinate‐curcumin (NC) can facilitate autophagic flux in THP‐1 cells induced by oxidized low‐density lipoprotein. Aims Given that autophagy plays critical roles in neurodegenerative diseases, the present study was carried out to investigate whether NC can improve cognitive function of rats with diabetes mellitus (DM) via restoring autophagic flux in CA1 hippocampus. Results Our results showed that NC treatment improved cognitive deficit and attenuated neuronal loss as well as cellular ultrastructure impairment in the CA1 region of DM rats induced by streptozotocin. Moreover, NC lowered the expressions of the apoptosis‐related proteins Bcl‐2, Bax, Cyt‐c, and cleaved Caspase‐3. Notably, NC treatment reversed autophagic flux impairment as evidenced by the deceases in LC3‐II and p62 protein levels, and autophagosome accumulation in the hippocampal CA1 region of DM rats. However, these protective effects of NC were abolished by cotreatment with 3‐methyladenine (an autophagy inhibitor) and chloroquine (an autophagic flux inhibitor), respectively. Furthermore, NC treatment decreased the expressions of phosphorylated mammalian target of rapamycin (mTOR) and p70 ribosomal protein S6 kinase (p70S6k) proteins in the CA1 region of DM rats. Conclusions These results indicate that NC ameliorates DM‐induced cognitive function impairment via restoring autophagic flux might by inhibiting mTOR/p70S6k activation in the CA1 region, and NC may be a promising agent for diabetic cognitive dysfunction prevention and treatment.