Neural Plasticity and Memory: Is Memory Encoded in Hydrogen Bonding Patterns?

被引:14
作者
Amtul, Zareen [1 ,2 ,3 ]
Rahman, Atta-ur [2 ,3 ]
机构
[1] Univ Western Ontario, Dept Psychiat, 800 Commissioners Rd East, London, ON N6A 5W9, Canada
[2] Univ Karachi, Int Ctr Chem & Biol Sci, HEJ Res Inst Chem, Karachi, Pakistan
[3] Univ Karachi, Int Ctr Chem & Biol Sci, Dr Panjwani Ctr Mol Med & Drug Res, Karachi, Pakistan
关键词
synaptic plasticity; hydrogen bond; memory encoding; glycoprotein; long-term potentiation; GILL-WITHDRAWAL REFLEX; CENTRAL-NERVOUS-SYSTEM; EXTRACELLULAR-MATRIX; VIBRATIONAL SPECTROSCOPY; INFRARED-SPECTROSCOPY; HUMAN HIPPOCAMPUS; CROSS-LINKING; AMYLOID-BETA; APLYSIA; BRAIN;
D O I
10.1177/1073858414547934
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Current models of memory storage recognize posttranslational modification vital for short-term and mRNA translation for long-lasting information storage. However, at the molecular level things are quite vague. A comprehensive review of the molecular basis of short and long-lasting synaptic plasticity literature leads us to propose that the hydrogen bonding pattern at the molecular level may be a permissive, vital step of memory storage. Therefore, we propose that the pattern of hydrogen bonding network of biomolecules (glycoproteins and/or DNA template, for instance) at the synapse is the critical edifying mechanism essential for short-and long-term memories. A novel aspect of this model is that nonrandom impulsive (or unplanned) synaptic activity functions as a synchronized positive-feedback rehearsal mechanism by revising the configurations of the hydrogen bonding network by tweaking the earlier tailored hydrogen bonds. This process may also maintain the elasticity of the related synapses involved in memory storage, a characteristic needed for such networks to alter intricacy and revise endlessly. The primary purpose of this review is to stimulate the efforts to elaborate the mechanism of neuronal connectivity both at molecular and chemical levels.
引用
收藏
页码:9 / 18
页数:10
相关论文
共 65 条
[1]   Hydrogen Bonding in Alzheimer's Amyloid-β; Fibrils Probed by 15N{17O} REAPDOR Solid-State NMR Spectroscopy [J].
Antzutkin, Oleg N. ;
Iuga, Dinu ;
Filippov, Andrei V. ;
Kelly, Robert T. ;
Becker-Baldus, Johanna ;
Brown, Steven P. ;
Dupree, Ray .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (41) :10289-10292
[2]   Bioactive natural products as a potential source of new pharmacophores. A theory of memory [J].
Atta-ur-Rahman ;
Choudhary, MI .
PURE AND APPLIED CHEMISTRY, 2001, 73 (03) :555-560
[3]   Biodiversity as a source of new pharmacophores: A new theory of memory. Part 3 [J].
Atta-ur-Rahman ;
Choudhary, MI .
PURE AND APPLIED CHEMISTRY, 2005, 77 (01) :75-81
[4]  
Atta-ur-Rahman, 2002, PURE APPL CHEM, V74, P511
[5]   STRUCTURAL-CHANGES ACCOMPANYING MEMORY STORAGE [J].
BAILEY, CH ;
KANDEL, ER .
ANNUAL REVIEW OF PHYSIOLOGY, 1993, 55 :397-426
[6]   Brain evolution studies go micro [J].
Balter, Michael .
SCIENCE, 2007, 315 (5816) :1208-1211
[7]  
BURLEY SK, 1988, ADV PROTEIN CHEM, V39, P125
[8]   Pore-Exposed Tyrosine Residues of P-Glycoprotein Are Important Hydrogen-Bonding Partners for Drugs [J].
Cakil, Yaprak Doenmez ;
Khunweeraphong, Narakorn ;
Parveen, Zahida ;
Schmid, Diethart ;
Artaker, Matthias ;
Ecker, Gerhard F. ;
Sitte, Harald H. ;
Pusch, Oliver ;
Stockner, Thomas ;
Chiba, Peter .
MOLECULAR PHARMACOLOGY, 2014, 85 (03) :420-428
[9]  
CASTELLUCCI V, 1970, SCIENCE, V167, P1745, DOI 10.1126/science.167.3926.1745
[10]   PRESYNAPTIC FACILITATION AS A MECHANISM FOR BEHAVIORAL SENSITIZATION IN APLYSIA [J].
CASTELLUCCI, V ;
KANDEL, ER .
SCIENCE, 1976, 194 (4270) :1176-1178