Bile Acid Signaling in Neurodegenerative and Neurological Disorders

被引:122
作者
Grant, Stephanie M. [1 ,2 ]
DeMorrow, Sharon [1 ,2 ,3 ]
机构
[1] Univ Texas Austin, Div Pharmacol & Toxicol, Coll Pharm, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Internal Med, Dell Med Sch, Austin, TX 78712 USA
[3] Cent Texas Vet Healthcare Syst, Res Div, Austin, TX 78712 USA
关键词
bile acid receptors; neuroprotective; tauroursodeoxycholic acid; ursodeoxycholic acid; alzheimer's disease; parkinson's disease; multiple sclerosis; hepatic encephalopathy; FARNESOID-X-RECEPTOR; VITAMIN-D-RECEPTOR; INDUCED MITOCHONDRIAL DYSFUNCTION; AMYOTROPHIC-LATERAL-SCLEROSIS; DYNAMIN-RELATED PROTEIN-1; SALT EXPORT PUMP; TAUROURSODEOXYCHOLIC ACID; URSODEOXYCHOLIC ACID; UDP-GLUCURONOSYLTRANSFERASES; GLUCOCORTICOID-RECEPTOR;
D O I
10.3390/ijms21175982
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
Bile acids are commonly known as digestive agents for lipids. The mechanisms of bile acids in the gastrointestinal track during normal physiological conditions as well as hepatic and cholestatic diseases have been well studied. Bile acids additionally serve as ligands for signaling molecules such as nuclear receptor Farnesoid X receptor and membrane-bound receptors, Takeda G-protein-coupled bile acid receptor and sphingosine-1-phosphate receptor 2. Recent studies have shown that bile acid signaling may also have a prevalent role in the central nervous system. Some bile acids, such as tauroursodeoxycholic acid and ursodeoxycholic acid, have shown neuroprotective potential in experimental animal models and clinical studies of many neurological conditions. Alterations in bile acid metabolism have been discovered as potential biomarkers for prognosis tools as well as the expression of various bile acid receptors in multiple neurological ailments. This review explores the findings of recent studies highlighting bile acid-mediated therapies and bile acid-mediated signaling and the roles they play in neurodegenerative and neurological diseases.
引用
收藏
页码:1 / 25
页数:25
相关论文
共 139 条
[1]   Ursodeoxycholic Acid Ameliorates Apoptotic Cascade in the Rotenone Model of Parkinson's Disease: Modulation of Mitochondrial Perturbations [J].
Abdelkader, Noha F. ;
Safar, Marwa M. ;
Salem, Hesham A. .
MOLECULAR NEUROBIOLOGY, 2016, 53 (02) :810-817
[2]   2018 Alzheimer's disease facts and figures [J].
不详 .
ALZHEIMERS & DEMENTIA, 2018, 14 (03) :367-425
[3]   Human bile salt export pump promoter is transactivated by the farnesoid X receptor/bile acid receptor [J].
Ananthanarayanan, M ;
Balasubramanian, N ;
Makishima, M ;
Mangelsdorf, DJ ;
Suchy, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (31) :28857-28865
[4]   FXR induces the UGT2B4 enzyme in hepatocytes: A potential mechanism of negative feedback control of FXR activity [J].
Barbier, O ;
Torra, IP ;
Sirvent, A ;
Claudel, T ;
Blanquart, C ;
Duran-Sandoval, D ;
Kuipers, F ;
Kosykh, V ;
Fruchart, JC ;
Staels, B .
GASTROENTEROLOGY, 2003, 124 (07) :1926-1940
[5]   Lipid-activated transcription factors control bile acid glucuronidation [J].
Barbier, Olivier ;
Trottier, Jocelyn ;
Kaeding, Jenny ;
Caron, Patrick ;
Verreault, Melanie .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2009, 326 (1-2) :3-8
[6]   On the mechanism of accumulation of cholestanol in the brain of mice with a disruption of sterol 27-hydroxylase [J].
Bavner, Ann ;
Shafaati, Marjan ;
Hansson, Magnus ;
Olin, Maria ;
Shpitzen, Shoshi ;
Meiner, Vardiella ;
Leitersdorf, Eran ;
Bjorkhem, Ingemar .
JOURNAL OF LIPID RESEARCH, 2010, 51 (09) :2722-2730
[7]   Chenodeoxycholic Acid Ameliorates AlCl3-Induced Alzheimer's Disease Neurotoxicity and Cognitive Deterioration via Enhanced Insulin Signaling in Rats [J].
Bazzari, Firas H. ;
Abdallah, Dalaal M. ;
El-Abhar, Hanan S. .
MOLECULES, 2019, 24 (10)
[8]   Ursodeoxycholic Acid Improves Mitochondrial Function and Redistributes Drp1 in Fibroblasts from Patients with Either Sporadic or Familial Alzheimer's Disease [J].
Bell, Simon M. ;
Barnes, Katy ;
Clemmens, Hannah ;
Al-Rafiah, Aziza R. ;
Al-ofi, Ebtisam A. ;
Leech, Vicki ;
Bandmann, Oliver ;
Shaw, Pamela J. ;
Blackburn, Daniel J. ;
Ferraiuolo, Laura ;
Mortiboys, Heather .
JOURNAL OF MOLECULAR BIOLOGY, 2018, 430 (21) :3942-3953
[9]   Pathophysiology of X-linked adrenoleukodystrophy [J].
Berger, J. ;
Forss-Petter, S. ;
Eichler, F. S. .
BIOCHIMIE, 2014, 98 :135-142
[10]   Bile acid metabolism is altered in multiple sclerosis and supplementation ameliorates neuroinflammation [J].
Bhargava, Pavan ;
Smith, Matthew D. ;
Mische, Leah ;
Harrington, Emily ;
Fitzgerald, Kathryn C. ;
Martin, Kyle ;
Kim, Sol ;
Reyes, Arthur Anthony ;
Gonzalez-Cardona, Jaime ;
Volsko, Christina ;
Tripathi, Ajai ;
Singh, Sonal ;
Varanasi, Kesava ;
Lord, Hannah-Noelle ;
Meyers, Keya ;
Taylor, Michelle ;
Gharagozloo, Marjan ;
Sotirchos, Elias S. ;
Nourbakhsh, Bardia ;
Dutta, Ranjan ;
Mowry, Ellen M. ;
Waubant, Emmanuelle ;
Calabresi, Peter A. .
JOURNAL OF CLINICAL INVESTIGATION, 2020, 130 (07) :3467-3482