Interleukin 6 reduces allopregnanolone synthesis in the brain and contributes to age-related cognitive decline in mice

被引:21
作者
Parks, Eileen E. [1 ,2 ]
Logan, Sreemathi [1 ,2 ,3 ]
Yeganeh, Alexander [1 ,2 ]
Farley, Julie A. [1 ,4 ]
Owen, Daniel B. [1 ,4 ]
Sonntag, William E. [1 ,2 ,4 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Oklahoma Ctr Gerosci & Hlth Brain Aging, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Oklahoma Ctr Neurosci, Oklahoma City, OK 73104 USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Rehabil Sci, Coll Allied Hlth, Oklahoma City, OK USA
[4] Univ Oklahoma, Hlth Sci Ctr, Dept Biochem & Mol Biol, Oklahoma City, OK 73104 USA
关键词
aging; Alzheimer's disease; inflammation; steroid hormones; enzyme regulation; progesterone; neurosteroid; cognitive function; STEROIDOGENIC ENZYMES; MOUSE MODEL; IN-VITRO; NEUROINFLAMMATION; EXPRESSION; PROTEINS; MEMORY; NEUROSTEROIDS; BIOSYNTHESIS; INHIBITION;
D O I
10.1194/jlr.RA119000479
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cognitive decline with age is a harmful process that can reduce quality of life. Multiple factors have been established to contribute to cognitive decline, but the overall etiology remains unknown. Here, we hypothesized that cognitive dysfunction is mediated, in part, by increased levels of inflammatory cytokines that alter allopregnanolone (AlloP) levels, an important neurosteroid in the brain. We assessed the levels and regulation of AlloP and the effects of AlloP supplementation on cognitive function in 4-month-old and 24-month-old male C57BL/6 mice. With age, the expression of enzymes involved in the AlloP synthetic pathway was decreased and corticosterone (CORT) synthesis increased. Supplementation of AlloP improved cognitive function. Interestingly, interleukin 6 (IL-6) infusion in young animals significantly reduced the production of AlloP compared with controls. It is notable that inhibition of IL-6 with its natural inhibitor, soluble membrane glycoprotein 130, significantly improved spatial memory in aged mice. These findings were supported by in vitro experiments in primary murine astrocyte cultures, indicating that IL-6 decreases production of AlloP and increases CORT levels. Our results indicate that age-related increases in IL-6 levels reduce progesterone substrate availability, resulting in a decline in AlloP levels and an increase in CORT. Furthermore, our results indicate that AlloP is a critical link between inflammatory cytokines and the age-related decline in cognitive function.
引用
收藏
页码:1308 / 1319
页数:12
相关论文
共 43 条
[1]   Sex differences in health and aging: a dialog between the brain and gonad? [J].
Austad, Steven N. .
GEROSCIENCE, 2019, 41 (03) :267-273
[2]   Age-related cognitive impairments in mice with a conditional ablation of the neural cell adhesion molecule [J].
Bisaz, Reto ;
Boadas-Vaello, Pere ;
Genoux, David ;
Sandi, Carmen .
LEARNING & MEMORY, 2013, 20 (04) :183-193
[3]   Composition and richness of the serum microbiome differ by age and link to systemic inflammation [J].
Buford, Thomas W. ;
Carter, Christy S. ;
VanDerPol, William J. ;
Chen, Dongquan ;
Lefkowitz, Elliot J. ;
Eipers, Peter ;
Morrow, Casey D. ;
Bamman, Marcas M. .
GEROSCIENCE, 2018, 40 (03) :257-268
[4]   Central inhibition of interleukin-6 trans-signaling during peripheral infection reduced neuroinflammation and sickness in aged mice [J].
Burton, Michael D. ;
Rytych, Jennifer L. ;
Freund, Gregory G. ;
Johnson, Rodney W. .
BRAIN BEHAVIOR AND IMMUNITY, 2013, 30 :66-72
[5]   Brain metabolism in health, aging, and neurodegeneration [J].
Camandola, Simonetta ;
Mattson, Mark P. .
EMBO JOURNAL, 2017, 36 (11) :1474-1492
[6]   Factors that positively or negatively mediate the effects of age on working memory across the adult life span [J].
Cansino, Selene ;
Torres-Trejo, Frine ;
Estrada-Manilla, Cinthya ;
Graciela Martinez-Galindo, Joyce ;
Hernandez-Ramos, Evelia ;
Ayala-Hernandez, Mariana ;
Gomez-Fernandez, Tania ;
Dolores Ramirez-Gonzalez, Maria ;
Ruiz-Velasco, Silvia .
GEROSCIENCE, 2018, 40 (03) :293-303
[7]   Cellular senescence and the aging brain [J].
Chinta, Shankar J. ;
Woods, Georgia ;
Rane, Anand ;
Demaria, Marco ;
Campisi, Judith ;
Andersen, Julie K. .
EXPERIMENTAL GERONTOLOGY, 2015, 68 :3-7
[8]   Neurosteroids: Biosynthesis and function of these novel neuromodulators [J].
Compagnone, NA ;
Mellon, SH .
FRONTIERS IN NEUROENDOCRINOLOGY, 2000, 21 (01) :1-56
[9]   Contribution of neuroinflammation and immunity to brain aging and the mitigating effects of physical and cognitive interventions [J].
Di Benedetto, Svetlana ;
Mueller, Ludmila ;
Wenger, Elisabeth ;
Duezel, Sandra ;
Pawelec, Graham .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2017, 75 :114-128
[10]   Age-Associated Changes in the Immune System and Blood-Brain Barrier Functions [J].
Erickson, Michelle A. ;
Banks, William A. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (07)