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Convergent Coding of Recent and Remote Fear Memory in the BLA

Alexandra Rosas

Created on November 28, 2023

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Convergent Coding of Recent and Remote Fear Memory in the Basolateral Amygdala

Jianfeng Liu, Michael S. Totty, Laila Melissari, Hugo Bayer, and Stephen Maren

Presentation by: Alexandra Rosas

BLA relevance to Fear memory (recent vs remote)

Introduction

Key Structures:

  • Amygdala
  • Basolateral amygdala
Previous figures:
  • Extracellular recordings show that single BLA neurons show robust increases in spike firing to both CSremote and CSrecent.
  • Fiber photometry recordings demonstrate that activity comes from principal neurons.
What next?

Fig 4

Hypothesis: Optogenetic silencing of bla principal neurons impairs short term memory, but not long term memory retrieval

Fig 4: Optoinhibition of BLA reduces freezing to both recent and remote CS in a within -subjects fear conditioning procedure.

4a

Experimental design

Methods

  • Bilateral injections into the BLA ( one week prior to remote conditioning):
  • Experimental group = Jaws (red shift inhibitory opsin)
    • AAV9-CaMKII-Jaws-GFP
  • Control Group = GFP virus
    • AAV9-CaMKII-GFP
  • Within-subject fear conditioning allows for comparison of neuronal and behavioral responses of recent and remote memories.

Timeline of the Experimental Design of Fig. 4

Day 1

Rats are microinjected with GFP or Jaws into the BLA.

Timeline of the Experimental Design of Fig. 4

Day 1

REMOTE CS: Subjects conditioned in context A.

<-*1 week*->

Day 7

Rats are microinjected with GFP or Jaws into the BLA.

Remote CS

  • Subjects placed in "Context A"
    • 3 min base line (BL)
    • Tone-foot shock pairing (5x)
      • CS remote:
        • 10 s
        • 80 dB
        • 8 kHz
      • Foot shock:
        • 1 mA
        • 2 s
    • 70 s intertrial intervals (ITI)
    • 60 s post shock period

Timeline of the Experimental Design of Fig. 4

Day 21

Day 1

REMOTE CS: Subjects conditioned in context A.

<-*2 weeks*->

RECENT CS: Subjects conditioned in context B.

Day 7

Rats are microinjected with GFP or Jaws into the BLA.

Recent CS

  • Subjects placed in "Context B"
    • 3 min base line (BL)
    • Tone-foot shock pairing (5x)
      • CS remote:
        • 10 s
        • 80 dB
        • 2 kHz
      • Foot shock:
        • 1 mA
        • 2 s
    • 70 sec intertrial intervals (ITI)
    • 60 sec post shock period

Timeline of the Experimental Design of Fig. 4

Day 21

Day 1

RETRIEVAL: 4 day counterbalancing procedure

REMOTE CS: Subjects conditioned in context A.

<-*1 day*->

RECENT CS: Subjects conditioned in context B.

Day 7

Day 22

Rats are microinjected with GFP or Jaws into the BLA.

Retrieval (Recent & Remote)

  • Conducted one day after CS recent in "Context C"
  • 4 day counterbalancing procedure
  • Each session:
    • 3 min BL
    • 5x Tone alone (either recent or remote)
    • 40 s ITIs
  • Bilateral red light illumination (635 nm)
    • Delivered 10 s before first tone onset, and persistet to end of testing session

Retrieval (Continued)

  • Day 1 (Day 22): CSrecent with light ON
  • Day 2 (Day 23): CSrecent with light OFF
  • Day 3 (Day 24): CSremote with light ON
  • Day 4 (Day 25): CSremote with light OFF

4b

Decreased firing rate due to Jaws.
  • 35 cells (recorded BLA neurons in Jaws rats)

4c

Micrograph of the fiber placement and viral expression in BLA.

4d-i

Freezing data of CSrecent and CSremote during BLA manipulation of Jaws and GFP infected rats.

Freezing Data from Fig. 4 (Continued)

vs

  • Rats expressing Jaws or GFP acquired similar levels of freezing during both CSrecent and CSremote.
    • Open circle = GFP (control group)
    • Filled circle = Jaws (experimental group)

Freezing Data from Fig. 4 (Continued)

vs

  • Continuous optoinhibition of Jaws subjects reduced freezing significantly.
    • Open circle = light OFF
    • Filled circle = light ON

Freezing Data from Fig. 4 (Continued)

vs

Fig. S3 & S4 from Supplemental Information

Fig. S4

Fig. S3

Fig 5

Hypothesis: Inhibitory PV interneurons in BLA are potent inhibitors for pyramidal neurons, thus acting as a constraint for fear memory ensembles.

Fig 5: Optogenetic stimulation of PV interneurons in the BLA reduces conditioned freezing to a remote CS.

5a

Experimental design

Methods used in Fig. 5a

  • Bilateral injections into the BLA of PV-cre transgenic mice (three weeks prior to remote conditioning):
  • Control Group = tdTomato
    • AAV8-FLEX-tdTomato
    • blank control virus
  • Experimental group = ChR2
    • AAV8-DIO-ChR2-mCherry
    • Cre-dependent excitatory opsin

Methods used in Fig. 5a

  • Within-subjects fear conditioning procedure (CS-US pairing in "Context A"):
    • 3 min base line (BL)
    • Tone-foot shock pairing (5x)
      • CS remote: 10 s, 80 dB, 2 kHz
      • Foot shock: 1 mA, 2 s
    • 70 s intertrial intervals (ITI)
    • 60 s post shock period
  • Remote memory retrieval tested 7 days later in "Context B":
    • Counterbalanced manner
    • Bilateral blue light illumination (450 nm)
      • Delivered 10 s before tone onset and terminated at tone offset
  • NOTE: No recent retrieval test conducted

5b

Micrograph depicting ChR2-mCherry expression and fiber placement.

5c

Micrograph showing that Cre-dependednt expression of ChR2-mCherry is specific to PV+ neurons.

5d-f

Freezing data of Cre-dependent rats infected with tdTomato and ChR2.
  • Fig. 5d: tdTomato and ChR2 show freezing patterns during conditioning.
  • Fig. 5e: During remote retrieval testing, optogenetic stimulation of BLA PV interneurons reduce freezing.
    • Open = laser OFF
    • Closed = laser ON
  • Fig. 5f: Analysis of Fig. 5e summarizing that optogenetic stimulation of PV neurons impaired fear memory retrieval.

Conclusion (Continued)

  • Optoinhibition of the BLA reduces freezing in both recent and remote CS in a within-subjects fear conditionig procedure
    • Supports findings of first three figures:
      • Convergent coding of recent and remote memory
      • Recent and remote memory induce similar levels of c-Fos expression and CS-caused Ca2+ in BLA neurons.
  • Optogenetic stimulation of PV interneurons in the BLA reduces conditioned freezing to a remote CS.
    • Recent memory not needed for remote memory retrieval.

Conclusion (Continued)

Possible shortcomings/issues:

  • Methological
  • Morphological
New directions:
  • Mechanisms behind function of BLA
  • Neuromodulators
  • Neuronal input to BLA during regulation of recent/remote memory retrieval.
Provides evidence that that BLA is a long term storage for emotional (fear) memory.

Works Cited

Liu, Jianfeng et al. “Convergent Coding of Recent and Remote Fear Memory in the Basolateral Amygdala.” Biological psychiatry vol. 91,9 (2022): 832-840. doi:10.1016/j.biopsych.2021.12.018Rajbhandari, Abha Karki. “Aversive Memory Storage in the Basolateral Amygdala: The Nut May Be Cracked.” Biological psychiatry vol. 91,9 (2022): e39-e40. doi:10.1016/j.biopsych.2022.02.958

Thank you :)

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Got an idea?

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With Genially templates, you can include visual resources to wow your audience. You can also highlight a particular sentence or piece of information so that it sticks in your audience’s minds, or even embed external content to surprise them: Whatever you like! Do you need more reasons to create dynamic content? No problem! 90% of the information we assimilate is received through sight and, what’s more, we retain 42% more information when the content moves.

  • Generate experiences with your content.
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