2021-01-15.txt 1.7 KB

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  1. Date: 2021-01-15
  2. Experiment: WT DREADD awake DG + CA3
  3. Experimenter: Mariela
  4. Objective: in awake
  5. 4x16 probe in DG
  6. 32 linear 50 um probe in CA3 at 20 deg angle
  7. SURGERIES
  8. Mouse 1: 4400 - 1 dot , DOB 13-12-2020 , 24.6 g
  9. injection: LV-160 / pLenti225.CamKII.hM4D(Gi)-mCherry
  10. Solutions: serum phy from Upcare
  11. 10:30 iso induction + bupre
  12. 11:30 Injection site = (0,0,0)==> DG marks (0.5;-0.5), (-0.5;0.5),
  13. CA3 marks at (1.5;0.25), (0.25,1.5) ==> center (0.79;0.78).
  14. 13:00 craniotomies good
  15. 13:05 Recovery
  16. RECORDINGS
  17. Mouse 1: 4400 - 1 dot , DOB 13-12-2020 , 24.6 g
  18. injection: LV-160 / pLenti225.CamKII.hM4D(Gi)-mCherry
  19. 14:30 Removed the silicon, OK
  20. 14:50 zero Q631 in the middle of the DG craniotomy
  21. zero CCO5 in the middle of the CA3 craniotomy
  22. take impedances
  23. Look for DS on probe Q631, ideally up in the depest shanks, and down on the shallow.
  24. Q631 (0;0;-2.5)
  25. 15:10 CA1
  26. Heard layer around 1100-1250 - not CA1 but very strong spikes
  27. Heard layer around 1350-1640 CA1
  28. SWR go up above the layer, and down below CA1.
  29. DS go down above the layer and up in the 2/3rd of the layer itself
  30. All deepst channel to be up and all the shallow to be down
  31. We want all up before 200uM
  32. granule cell layer - spikes on :
  33. 2340-2450- shank 1
  34. 2370-2500- shank 2
  35. 2360-2500- shank 3
  36. 2390-2500- shank 4
  37. Reversal seems to happen within the upper part of the DG cellular layer.
  38. 16:20 CCO5 (0;0;-2.32)
  39. 1570-1670 CA1
  40. CA3
  41. 2190-
  42. 16:30 Recording 1
  43. 17:00 Inject 100uL CNO + recording 2
  44. A47 channel seems broken
  45. 17:30 Recording 3
  46. 17:50 remove probes
  47. 17:55 iso 5% - sac
  48. Notes for histology:
  49. 4400
  50. CA3: 20 deg, DiI (1*1 marks total)
  51. DG: 0 deg, DiI x (1*4 marks total)
  52. TdTomato