|
1 Introduction: Fundamental Concepts and Historical Foundations |
|
|
1 | (16) |
|
Learning and Memory Are Theoretical Concepts |
|
|
2 | (1) |
|
Psychological and Neurobiological Approaches |
|
|
3 | (3) |
|
|
3 | (2) |
|
|
5 | (1) |
|
Historical Influences: The Golden Age |
|
|
6 | (7) |
|
|
6 | (3) |
|
The Neuron Doctrine and Synaptic Plasticity |
|
|
9 | (2) |
|
|
11 | (2) |
|
|
13 | (1) |
|
|
13 | (1) |
|
|
13 | (1) |
|
Neural Systems and Memory |
|
|
14 | (1) |
|
|
14 | (1) |
|
|
14 | (3) |
|
PART 1 Synaptic Basis of Memory |
|
|
17 | (134) |
|
2 Memory and the Brain: Central Concepts |
|
|
19 | (28) |
|
|
20 | (1) |
|
The Phenomenon of Long-Term Potentiation |
|
|
21 | (15) |
|
The Conceptual Basis of LTP |
|
|
24 | (8) |
|
Methodology for Inducing and Measuring LTP |
|
|
32 | (3) |
|
Long-Term Depression: The Polar Opposite of LTP |
|
|
35 | (1) |
|
How Synapses Are Modified |
|
|
36 | (4) |
|
The Synapse as a Biochemical Factory |
|
|
36 | (3) |
|
|
39 | (1) |
|
An Organizing Framework: Three Principles |
|
|
40 | (3) |
|
The Duration of LTP Can Vary |
|
|
41 | (1) |
|
Molecular Processes Determine LTP Durability |
|
|
42 | (1) |
|
Synapses Are Strengthened and Maintained in Stages |
|
|
42 | (1) |
|
|
43 | (1) |
|
|
44 | (3) |
|
3 Generating Long-Term Potentiation |
|
|
47 | (20) |
|
The Role of Glutamate Receptors |
|
|
48 | (6) |
|
LTP Induction Requires NMDA Receptors |
|
|
49 | (2) |
|
Two Events Open the NMDA Channel |
|
|
51 | (1) |
|
Increase in AMPA Receptors Supports LTP Expression |
|
|
51 | (3) |
|
Post-Translation Processes |
|
|
54 | (9) |
|
AMPA Receptor Trafficking |
|
|
54 | (7) |
|
Actin Cytoskeleton Degradation |
|
|
61 | (2) |
|
|
63 | (1) |
|
|
63 | (4) |
|
4 Stabilizing Long-Term Potentiation |
|
|
67 | (22) |
|
Structural Changes in Dendritic Spines Support LTP |
|
|
68 | (3) |
|
Stabilizing LTP Requires Actin Polymerization |
|
|
71 | (3) |
|
Phase 1 Actin Filaments Are Unbundled and Severed |
|
|
72 | (2) |
|
Phase 2 The Actin--Spine Architecture Is Reconstructed |
|
|
74 | (1) |
|
|
74 | (10) |
|
|
75 | (2) |
|
TBS Induces Actin Regulation |
|
|
77 | (2) |
|
Cell Adhesion Molecules Help Stabilize the Trace |
|
|
79 | (5) |
|
|
84 | (1) |
|
|
84 | (5) |
|
5 Consolidating LTP: Translation and Transcription |
|
|
89 | (18) |
|
The De Novo Protein Synthesis Hypothesis |
|
|
90 | (1) |
|
|
91 | (3) |
|
|
94 | (5) |
|
Synapse-to-Nucleus Signaling |
|
|
94 | (3) |
|
Soma-to-Nucleus Signaling |
|
|
97 | (2) |
|
Translation Requires Increased Calcium Levels |
|
|
99 | (5) |
|
Spine and Dendritic Compartments |
|
|
101 | (2) |
|
|
103 | (1) |
|
|
104 | (1) |
|
|
104 | (3) |
|
6 Consolidating LTP: Specific Mechanisms |
|
|
107 | (24) |
|
Local Dendritic mRNA Dynamics |
|
|
108 | (5) |
|
Initiation of Local Protein Synthesis |
|
|
109 | (2) |
|
|
111 | (2) |
|
|
113 | (3) |
|
The Ubiquitin--Proteasome System |
|
|
113 | (1) |
|
Protein Degradation and LTP |
|
|
114 | (2) |
|
|
116 | (2) |
|
Arc Antisense Blocks Long-Lasting LTP |
|
|
116 | (1) |
|
BDNF--TrkB Consolidation Depends on Arc Protein Synthesis |
|
|
117 | (1) |
|
Arc Protein Sustains Actin Regulation |
|
|
117 | (1) |
|
The Clustered Plasticity Model |
|
|
118 | (8) |
|
Synaptic Tags and the Regulation of Spine Clusters |
|
|
121 | (3) |
|
|
124 | (1) |
|
|
125 | (1) |
|
|
125 | (1) |
|
|
126 | (1) |
|
|
127 | (4) |
|
7 Maintaining Long-Term Potentiation |
|
|
131 | (14) |
|
|
133 | (6) |
|
|
133 | (1) |
|
|
134 | (5) |
|
Redundancy and Compensation |
|
|
139 | (2) |
|
|
141 | (1) |
|
|
141 | (1) |
|
|
142 | (1) |
|
|
142 | (3) |
|
8 Bringing It All Together |
|
|
145 | (6) |
|
|
146 | (1) |
|
|
147 | (1) |
|
|
148 | (1) |
|
|
149 | (1) |
|
|
150 | (1) |
|
PART 2 Molecules and Memory |
|
|
151 | (144) |
|
9 Making Memories: Conceptual Issues and Methodologies |
|
|
153 | (22) |
|
|
154 | (1) |
|
|
154 | (3) |
|
Test Behavior: The Window to the Memory Trace |
|
|
155 | (2) |
|
The Learning--Performance Distinction |
|
|
157 | (1) |
|
Dimensions of Memory Traces |
|
|
157 | (2) |
|
The Concept of Memory Consolidation |
|
|
159 | (1) |
|
Electroconvulsive Shock and Memory Disruption |
|
|
159 | (1) |
|
Memory Disruption: A Storage or Retrieval Failure? |
|
|
159 | (1) |
|
Some Behavioral Test Methods for Studying Memory |
|
|
160 | (7) |
|
Inhibitory Avoidance Conditioning |
|
|
161 | (1) |
|
|
162 | (2) |
|
Spatial Learning in a Water-Escape Task |
|
|
164 | (2) |
|
|
166 | (1) |
|
Methods for Manipulating Brain Function |
|
|
167 | (5) |
|
|
167 | (1) |
|
|
168 | (4) |
|
|
172 | (1) |
|
|
172 | (3) |
|
10 Memory Formation: Early Stages |
|
|
175 | (26) |
|
NMDA Receptors and Memory Formation |
|
|
176 | (7) |
|
Pharmacological Alteration |
|
|
176 | (2) |
|
|
178 | (3) |
|
|
181 | (2) |
|
AMPA Receptors and Memory Formation |
|
|
183 | (4) |
|
Fear Conditioning Drives GluA1 AMPA Receptors into Spines |
|
|
183 | (2) |
|
Preventing AMPA Receptor Trafficking Impairs Fear Conditioning |
|
|
185 | (1) |
|
Ampakines and Cognitive Enhancement |
|
|
186 | (1) |
|
NMDA and AMPA Receptors: Acquisition and Retrieval |
|
|
187 | (2) |
|
CaMKII and Memory Formation |
|
|
189 | (3) |
|
Preventing Autophosphorylation of CaMKII Impairs Learning |
|
|
189 | (1) |
|
|
190 | (2) |
|
Actin Dynamics and Memory Formation |
|
|
192 | (1) |
|
Working and Reference Memory |
|
|
192 | (4) |
|
|
193 | (1) |
|
Critical Contributions of Glutamate Receptor Subunits |
|
|
194 | (2) |
|
|
196 | (1) |
|
|
197 | (4) |
|
|
201 | (20) |
|
|
202 | (2) |
|
Criterion for When the Memory is Consolidated |
|
|
204 | (1) |
|
Inhibiting Protein Synthesis |
|
|
204 | (2) |
|
Molecular Basis of Consolidation |
|
|
206 | (11) |
|
Local Protein Synthesis: The First Wave |
|
|
206 | (5) |
|
Genomic Signaling: The Second Wave |
|
|
211 | (6) |
|
Protein Degradation Processes |
|
|
217 | (1) |
|
|
218 | (1) |
|
|
218 | (3) |
|
12 Memory Modulation Systems |
|
|
221 | (22) |
|
Memory Modulation Framework |
|
|
222 | (1) |
|
The Great Modulator: The Basolateral Amygdala |
|
|
223 | (2) |
|
|
225 | (2) |
|
The Epinephrine Vagus Connection |
|
|
227 | (6) |
|
Norepinephrine Enhances Memories |
|
|
230 | (1) |
|
Norepinephrine Enhances Glutamate Release and Arc Translation |
|
|
230 | (3) |
|
The Norepinephrine Signal in Other Storage Areas |
|
|
233 | (1) |
|
The Epinephrine Liver-Glucose Connection |
|
|
233 | (4) |
|
Bioenergetics and the Brain |
|
|
233 | (1) |
|
|
234 | (1) |
|
|
235 | (1) |
|
Glucose and Transcription |
|
|
235 | (2) |
|
Glucocorticoids: The Other Adrenal Hormones |
|
|
237 | (1) |
|
|
238 | (1) |
|
|
239 | (4) |
|
13 The Yin and Yang of Memory: Forgetting versus Maintenance |
|
|
243 | (16) |
|
Psychological View of Forgetting |
|
|
244 | (1) |
|
Neurobiology of Forgetting: The Yin |
|
|
244 | (7) |
|
Calcium Signaling Regulates Forgetting |
|
|
245 | (1) |
|
AMPA Receptor Endocytosis |
|
|
246 | (1) |
|
Mediators of Calcium Signaling |
|
|
246 | (5) |
|
Memory Maintenance: The Yang |
|
|
251 | (3) |
|
|
251 | (1) |
|
Interfering with PKMσ Erases a Taste-Aversion Memory |
|
|
252 | (1) |
|
PKMσ Strengthens New Memories and Prevents Forgetting |
|
|
253 | (1) |
|
PKMσ Prevents AMPA Receptor Endocytosis |
|
|
253 | (1) |
|
Epilogue: Why Do We Forget or Remember? |
|
|
254 | (1) |
|
|
255 | (1) |
|
|
255 | (4) |
|
|
259 | (16) |
|
The Engram Search: A Story of Technical Advances |
|
|
261 | (6) |
|
|
263 | (1) |
|
|
263 | (3) |
|
|
266 | (1) |
|
Dynamics of Engram Formation |
|
|
267 | (2) |
|
What Gets to Be an Engram Cell? |
|
|
269 | (3) |
|
|
272 | (1) |
|
|
272 | (3) |
|
15 The Fate of Retrieved Memories |
|
|
275 | (20) |
|
|
276 | (3) |
|
|
276 | (1) |
|
|
277 | (2) |
|
|
279 | (7) |
|
|
281 | (1) |
|
What Triggers Destabilization? |
|
|
282 | (2) |
|
Destabilization, Repetition, and Integration |
|
|
284 | (1) |
|
Destabilization without Behavioral Expression |
|
|
285 | (1) |
|
Integration Theory and Amnesia |
|
|
286 | (1) |
|
Memory Erasure: A Potential Therapy |
|
|
287 | (4) |
|
|
288 | (1) |
|
|
289 | (2) |
|
|
291 | (1) |
|
|
292 | (3) |
|
PART 3 Neural Systems and Memory |
|
|
295 | (108) |
|
16 Memory Systems and the Hippocampus |
|
|
297 | (20) |
|
The Multiple Memory Systems Perspective |
|
|
298 | (2) |
|
Example 1 Personal Facts and Emotions |
|
|
298 | (1) |
|
Example 2 Personal Facts and Skills |
|
|
298 | (2) |
|
The Case of Henry Molaison |
|
|
300 | (2) |
|
The Episodic Memory System |
|
|
302 | (5) |
|
The Animal Model Strategy |
|
|
302 | (3) |
|
Studies of Patients with Selective Hippocampal Damage |
|
|
305 | (2) |
|
The DNMS Paradox Resolved |
|
|
307 | (1) |
|
The MTH System: Episodic Memory and Semantic Memory |
|
|
308 | (2) |
|
|
310 | (2) |
|
Growing Up without the Hippocampus |
|
|
310 | (1) |
|
Recognition Memory and MTH Modularity |
|
|
311 | (1) |
|
|
312 | (1) |
|
|
313 | (4) |
|
17 The Hippocampus Index and Episodic Memory |
|
|
317 | (24) |
|
Properties of Episodic Memory |
|
|
318 | (2) |
|
Conscious Recollection and Contextual Information Storage |
|
|
318 | (1) |
|
Automatic Capture of Episodic and Incidental Information |
|
|
319 | (1) |
|
Single Episode Capture with Protection from Interference |
|
|
319 | (1) |
|
|
320 | (1) |
|
A Neural System that Supports Episodic Memory |
|
|
320 | (2) |
|
The Hierarchy and the Loop |
|
|
320 | (2) |
|
|
322 | (1) |
|
The Indexing Theory of Episodic Memory |
|
|
322 | (4) |
|
Pattern Completion and Pattern Separation |
|
|
324 | (1) |
|
Why Not Just Store the Memory in the Neocortex? |
|
|
324 | (2) |
|
Indexing Theory and Properties of Episodic Memory |
|
|
326 | (1) |
|
Evidence for the Indexing Theory |
|
|
326 | (11) |
|
|
327 | (1) |
|
Context Representations Depend on the Hippocampus |
|
|
327 | (3) |
|
Conscious Awareness and Recollection |
|
|
330 | (1) |
|
Automatic Capture of Single Episodes |
|
|
330 | (1) |
|
|
331 | (1) |
|
|
332 | (5) |
|
|
337 | (1) |
|
|
338 | (3) |
|
|
341 | (18) |
|
The Standard Model of Systems Consolidation |
|
|
342 | (2) |
|
Evaluating the Standard Model |
|
|
344 | (8) |
|
|
344 | (2) |
|
|
346 | (1) |
|
Damage to the Hippocampus Disrupts Old and New Memories |
|
|
346 | (2) |
|
Memory without the Hippocampus |
|
|
348 | (3) |
|
|
351 | (1) |
|
Systems Consolidation: Another Look |
|
|
352 | (2) |
|
|
354 | (1) |
|
|
355 | (4) |
|
19 Actions, Habits, and the Cortico-Striatal System |
|
|
359 | (24) |
|
The Concept of Instrumental Behavior |
|
|
360 | (2) |
|
Two Theories of Instrumental Behavior |
|
|
362 | (1) |
|
Thorndike's Law of Effect |
|
|
362 | (1) |
|
Tolman's Cognitive Expectancy Theory |
|
|
362 | (1) |
|
|
363 | (8) |
|
With Practice, Actions Become Habits |
|
|
367 | (1) |
|
A Conceptual Model for Actions and Habits |
|
|
368 | (1) |
|
Action and Habit Systems Compete |
|
|
369 | (1) |
|
Action Systems Are Vulnerable |
|
|
370 | (1) |
|
A Cortico-Striatal System Supports Instrumental Behavior |
|
|
371 | (7) |
|
Neural Support for Actions |
|
|
372 | (4) |
|
Neural Support for Habits |
|
|
376 | (2) |
|
The Striatum Stores Action and Habit Memories |
|
|
378 | (1) |
|
The Neural Basis of Rewarding Outcomes |
|
|
378 | (2) |
|
|
380 | (1) |
|
|
381 | (2) |
|
20 Learning about Danger: The Neurobiology of Fear Memories |
|
|
383 | (20) |
|
|
384 | (2) |
|
|
386 | (3) |
|
Eliminating Maladaptive Fears: Theories of Extinction |
|
|
389 | (3) |
|
Neural Basis of Fear Extinction |
|
|
392 | (6) |
|
The CS--noUS Neural Circuit |
|
|
392 | (1) |
|
Why Fear Renews: A Role for the Hippocampus |
|
|
393 | (1) |
|
Why Fear Spontaneously Recovers: A Role for Forgetting |
|
|
394 | (1) |
|
Extinction Learning Depends on NMDA Receptors |
|
|
394 | (2) |
|
Extinction Can Erase Fear Memories |
|
|
396 | (2) |
|
Defensive Circuits and the Concept of Fear |
|
|
398 | (1) |
|
|
398 | (1) |
|
|
399 | (4) |
Glossary |
|
403 | (16) |
Index |
|
419 | |