Τόμος 26 (2012) – Τεύχος 2 – Άρθρο 5 – Επιθεώρηση Κλινικής Φαρμακολογίας και Φαρμακοκινητικής-Διεθνής Έκδοση – Volume 26 (2012) – Issue 2 – Article 5 – Epitheorese Klinikes Farmakologias και Farmakokinetikes-International Edition

Title Endogenous neurogenesis and Alzheimer’s disease: topics in regenerative medicine
Authors Vassiliki-Sofia Grech1, Maria Grech2, Antonios Togias3 and Ioanna Grech4

1. Bachelor of Medical Biochemistry, King’s College University, Student of Medicine, Medical University of Pecs, Hungary

2. Medical Resident in Pediatrics, Children’s Hospital Aglaia Kyriakou, Athens, Hellas

3. Medical Resident in Pediatrics, General Hospital of Kalamata

4. Technological Education Institution of Athens, Egaleo, Athens, Hellas

Citation Grech, V.-S., Grech, M., Togias, A., Grech, I.: Endogenous neurogenesis and Alzheimer’s disease: topics in regenerative medicine, Epitheorese Klin. Farmakol. Farmakokinet. 26(2): 109-122 (2012)
Publication Date Accepted for publication (Final Version): July 1, 2012
Full Text Language English
Order – Buy  Ηλεκτρονική Μορφή: pdf (10 €) – Digital Type: pdf (10 €)

pharmakonpress[at]pharmakonpress[.]gr

Keywords Alzheimer’s Disease, epidemiology, statistics, neuropathology, endogenous neurogenesis, adult brain, future prospects.
Other Terms Review article
Summary Alzheimer’s Disease (AD) is the most prevalent form of Dementia, which is a gradual loss of memory, judgment, and ability to function and the sixth leading cause of death in Developed World. This disorder usually appears in people older than age 65, but less common forms of the disease appear earlier in adulthood. Research advances have enabled detailed understanding of the molecular pathogenesis of the hallmarks of the disease, i.e., plaques, composed of amyloid bet, and tangles, composed of hyperphosphorylated tau. Mutations in the amyloid precursor protein, presenilin 1 and presenilin 2 genes cause autosomal dominant familial Alzheimer’s disease (AD). PSEN1 and PSEN2 are essential components of the gamma-secretase complex, which cleaves APP to affect Abeta processing. Recent advances in develop-mental and stem cell biology have made regeneration-based therapies feasible as therapeutic strategies for patients with damaged central nervous systems, including those with spinal cord injuries, Parkinson disease, or stroke. This review provides information meant to increase an understanding of the public-health impact of AD, including incidence and prevalence, mortality, lifetime risks, costs, impact on family caregivers, AD neuropathology, endogenous neurogenesis in adult brain and future prospects.
References 1. Gouras G.K., Almeida C.G., Takahashi R.H.: Intraneuronal Abeta accumulation and origin of plaques in Alzheimer’s disease. Neurobiol. Aging 26: 1235-1244 (2005)

2. Butterfield D.A., Drake J., Pocernich C., Castegna A.: Evidence of oxidative damage in Alzheimer’s disease brain: central role for amyloid beta-peptide. Trends Mol. Med. 7: 548-554 (2001)

3. United States of America Alzheimer’s Association: 2009 Alzheimer’s Disease Facts and Figures. Alzheimers Dement. 5: 234-270 (2009)

4. http://www.alzheimers-reseach.org.uk,

  http://www.nhs.uk/conditions/alzheimers-disease

5. Blennow K., de Leon M.J., Zetterberg H.: Alzheimer’s disease. Lancet 368: 387-403 (2006)

6. Whitmer R.A., Gunderson E.P., Barrett-Connor E., Quesenberry C.P.,Jr., Yaffe K.: Obesity in middle age and future risk of dementia: a 27 year longitudinal population based study. BMJ 330: 1360 (2005)

7. Whitmer R.A., Gustafson D.R., Barrett-Connor E., Haan M.N., Gunderson E.P., Yaffe K.: Central obesity and increased risk of dementia more than three decades later. Neurology 71: 1057-1064 (2008)

8. Norton M.C., Smith K.R., Ostbye T., Tschanz J.T., Schwartz S., Corcoran C., Breitner J.C., Steffens D.C., Skoog I., Rabins P.V., Welsh-Bohmer K.A.: Early parental death and remarriage of widowed parents as risk factors for Alzheimer disease: the Cache County study. Am. J. Geriatr. Psychiatry 19: 814-824 (2011)

9. Reddy P.H.: Amyloid precursor protein-mediated free radicals and oxidative damage: implications for the development and progression of Alzheimer’s disease. J. Neurochem. 96: 1-13 (2006)

10. Takei H., Kosarac O., Powell S.Z.: Cytomorphologic manifestations of Alzheimer’s disease using brain squash smears: An autopsy study with histology-cytology correlation. Diagn. Cytopathol.37: 645-660 (2009)

11. Chan D., Fox N.C., Scahill R.I., Crum W.R., Whitwell J.L., Leschziner G., Rossor A.M., Stevens J.M., Cipolotti L., Rossor M.N.: Patterns of temporal lobe atrophy in semantic dementia and Alzheimer’s disease. Ann. Neurol. 49: 433-442 (2001)

12. Anastasio T.J.: Data-driven modeling of Alzheimer Disease pathogenesis. J. Theor. Biol. 290C: 60-72 (2011)

13. Tsuang D., Larson E.B., Bolen E., Thompson M.L., Peskind E., Bowen J., McCormick W., Teri L., Kukull W., Vavrek D., et al.: Visual hallucinations in dementia: a prospective community-based study with autopsy. Am. J. Geriatr. Psychiatry 17: 317-323 (2009)

14 Rossner S., Sastre M., Bourne K., Lichtenthaler S.F.: Transcriptional and translational regulation of BACE1 expression-implications for Alzheimer’s disease. Prog. Neuro-biol. 79: 95-111 (2006)

15. Shepherd C., McCann H., Halliday G.M.: Variations in the neuropathology of familial Alzheimer’s disease. Acta Neuropathol. 118: 37-52 (2009)

16. Bitan G., Kirkitadze M.D., Lomakin A., Vollers S.S., Benedek G.B., Teplow D.B.: (2003). Amyloid beta-protein (Abeta) assembly: Abeta 40 and Abeta 42 oligomerize through distinct pathways. Proc. Natl. Acad. Sci. USA 100: 330-335 (2003)

17. Crouch P.J., Harding S.M., White A.R., Camakaris J., Bush A.I., Masters C.L.: Mechanisms of A beta mediated neurodegeneration in Alzheimer’s disease. Int. J. Biochem. Cell Biol. 40, 181-198 (2008)

18. Mandelkow E., von Bergen M., Biernat J., Mandelkow E.M.: Structural principles of tau and the paired helical filaments of Alzheimer’s disease. Brain Pathol. 17: 83-90 (2007)

19. Crook R., Verkkoniemi A., Perez-Tur J., Mehta N., Baker M., Houlden H., Farrer M., Hutton M., Lincoln S., Hardy J., et al.: A variant of Alzheimer’s disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1. Nat. Med. 4: 452-455 (1998)

20. Williamson J., Goldman J., Marder K.S.: Genetic aspects of Alzheimer disease. Neurologist 15: 80-86 (2009)

21. Raber, J., Huang, Y., and Ashford, J.W.: ApoE genotype accounts for the vast majority of AD risk and AD pathology. Neurobiol. Aging 25: 641-650 (2004)

22. Strittmatter W.J., Weisgraber K.H., Huang D.Y., Dong L.M., Salvesen G.S., Pericak-Vance M., Schmechel D., Saunders A.M., Goldgaber D., Roses A.D.: Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer disease. Proc. Natl. Acad. Sci USA 90: 8098-8102 (1993)

23. Nagy Z., Esiri M.M., Jobst K.A., Johnston C., Litchfield S., Sim E., Smith A.D.: Influence of the apolipoprotein E genotype on amyloid deposition and neurofibrillary tangle formation in Alzheimer’s disease. Neuroscience 69: 757-761 (1995)

24. Spires T.L., Hyman B.T.: Transgenic Models of Alzheimer’s Disease: Learning from Animals. NeuroRx 2: 423-437 (2005)

25 Raber J., Wong D., Buttini M., Orth M., Bellosta S., Pitas R.E., Mahley R.W., Mucke L.: Isoform-specific effects of human apolipoprotein E on brain function revealed in ApoE knockout mice: increased susceptibility of females. Proc. Natl. Acad. USA 95: 10914-10919 (1998)

26. Asai M., Yagishita S., Iwata N., Saido T.C., Ishiura S., Maruyama K.: An alternative metabolic pathway of amyloid precursor protein C-terminal fragments via cathepsin B in a human neuroglioma model. FASEB J. 25: 3720-3730 (2011)

27. Okano H., Sakaguchi M., Ohki K., Suzuki N., Sawamoto K.: Regeneration of the central nervous system using endogenous repair mechanisms. J. Neurochem. 102: 1459-1465 (2007)

28. Steiner B., Wolf S., Kempermann G.: Adult neurogenesis and neurodegenerative disease. Regen. Med. 1: 15-28 (2006)

29. Elder G.A., De Gasperi R., Gama Sosa M.A.: Research update: neurogenesis in adult brain and neuropsychiatric disorders. Mt. Sinai J. Med. 73: 931-940 (2006)

30. Hagg T.: From neurotransmitters to neurotrophic factors to neurogenesis. Neuroscientist 15: 20-27 (2009)

31. Pencea V., Bingaman K.D., Freedman L.J., Luskin M.B.: Neurogenesis in the subventricular zone and rostral migratory stream of the neonatal and adult primate forebrain. Exp. Neurol. 172: 1-16 (2001)

32. Schwob J.E.: Neural regeneration and the peripheral olfactory system. Anat. Rec. 269: 33-49 (2002)

33. Eriksson P.S., Perfilieva E., Bjork-Eriksson T., Alborn A.M., Nordborg C., Peterson D.A., Gage F.H. Neurogenesis in the adult human hippocampus. Nat. Med. 4: 1313-1317 (1998)

34. Lazarov O., Mattson M.P., Peterson D.A., Pimplikar S.W., van Praag H.: When neurogenesis encounters aging and disease. Trends Neurosci. 33: 569-579 (2011)

35. Abdel-Salam O.M.:  Stem cell therapy for Alzheimer’s disease. CNS Neurol. Disord. Drug Targets 10: 459-485 (2011)

36. Minger S.L., Ekonomou A., Carta E.M., Chinoy A., Perry R.H., Ballard C.G.: Endogenous neurogenesis in the human brain following cerebral infarction. Regen. Med. 2: 69-74 (2007)

37. Quiñones-Hinojosa A., Sanai N., Soriano-Navarro M., Gonzalez-Perez O., Mirzadeh Z., Gil-Perotin S., Romero-Rodriguez R., Berger M.S., Garcia-Verdugo J.M., Alvarez-Buylla A.: Cellular composition and cytoarchitecture of the adult human subventricular zone: a niche of neural stem cells. J. Comp. Neurol. 494: 415-434 (2006)

38. Gould E., Tanapat P. McEvent B.S., Flügge G., Fuchs E.: Proliferation of granule cell precursors in the dentate gyrus of adult monkeys is diminished by stress. Proc. Natl. Acad. Sci. USA 95: 3168-3171 (1998)

39. Rodriguez J.J., Jones V.C., Tabuchi M., Allan S.M., Knight E.M., LaFerla F.M., Oddo S., Verkhratsky A.: Impaired adult neurogenesis in the dentate gyrus of a triple transgenic mouse model of Alzheimer’s disease. PLoS ONE 3: e2935 (2008)

40. Yaffe K., Cauley J., Sands L., Browner W.: Apolipoprotein E phenotype and cognitive decline in a prospective study of elderly community women. Arch. Neurol. 54: 1110-1114 (1997)

41. Enciu A.M., Nicolescu M.I., Manole C.G., Muresanu D.F., Popescu L.M., Popescu B.O.: Neuroregeneration in neurodegenerative disorders. BMC Neurol. 11: 75 (2011)

42. Ziabreva I., Perry E., Perry R., Minger S.L., Ekonomou A., Przyborski S., Ballard C.: Altered neurogenesis in Alz-heimer’s disease. J. Psychosom. Res. 61: 311-316 (2006)

43. Francis P.T., Palmer A.M., Snape M., Wilcock G.K.: The cholinergic hypothesis of Alzheimer’s disease: a review of progress. J. Neurol. Neurosurg. Psychiatry 66: 137-147 (1999)

44. Jin K., Peel A.L., Mao X.O., Xie L., Cottrell B.A., Henshall D.C., Greenberg D.A.: Increased hippocampal neurogenesis in Alzheimer’s disease. Proc. Natl. Acad. Sci. USA 101: 343-347 (2004)

45. Leow A.D., Yanovsky I., Parikshak N., Hua X., Lee S., Toga A.W., Jack C.R.,Jr, Bernstein M.A., Britson P.J., Gunter J.L., Ward C.P., Borowski B., Shaw L.M., Trojanowski J.Q., Fleisher A.S., Harvey D., Kornak J., Schuff N., Alexander G.E., Weiner M.W., Thompson P.M., Alzheimer’s Disease Neuroimaging Initiative: Alzheimer’s disease neuroimaging initiative: a one-year follow up study using tensor-based morphometry correlating degenerative rates, bio-markers and cognition. Neuroimage 45: 645-655 (2009)

46. Zhongling Feng, Gang Zhao, Lei Yu.: Neural stem cells and Alzheimer’s disease: challenges and hope. Am. J. Alzheimer’s Dis., Other Demen. 24: 52-57 (2009)

Relative Papers

Online ISSN 1011-6575

 

Bookmark the permalink.

Comments are closed.