Long‐Lived Organotypic Slice Culture Model of the Rat Basolateral Amygdala. Issue 10 (20th October 2021)

• Record Type: Journal Article
• Authors: Michaelson, Sheldon D.; Müller, Taylor M.; Bompolaki, Maria; Miranda Tapia, Ana Pamela; Villarroel, Heika Silveira; Mackay, James P.; Balogun, Pauline J.; Urban, Janice H.; Colmers, William F.
• Is Part Of: Current protocols. Volume 1:Issue 10(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-10-20
• Subjects: basolateral amygdala -- dendritic structure -- electrophysiological properties -- hypotrophy -- neuropeptide Y -- organotypic slice culture; Life sciences -- Laboratory manuals -- Periodicals; Biology -- Laboratory manuals -- Periodicals; Life sciences -- Technique -- Periodicals; Biology -- Technique -- Periodicals; 570.028
• DOI: 10.1002/cpz1.267
• Languages: English
• ISSNs: 2691-1299

Abstract

Abstract: Organotypic slice cultures (OTCs) have been employed in the laboratory since the early 1980s and have proved to be useful for the study of a number of neural systems. Our recent work focuses on the development of behavioral stress resilience induced by repeated daily injections of neuropeptide Y into the basolateral amygdala (BLA). Resilience develops over weeks, persisting to 8 weeks. To unravel the cellular mechanisms underlying neuropeptide Y–induced stress resilience we developed in vitro OTCs of the BLA. Here, we provide an optimized protocol that consistently yields viable and healthy OTCs containing the BLA and surrounding tissue using the interface method, prepared with slices taken from postnatal (P) day 14 rats. We explain key points to optimizing tissue viability and discuss mitigation or avoidance of pitfalls that can arise to aid in successful implementation of this technique. We show that principal neurons in BLA OTCs (8 weeks in vitro = equivalent postnatal day 70) develop into networks that are electrophysiologically very similar to those from acute slices obtained from older rats (P70) and respond to pharmacological treatments in a comparable way. Furthermore, we highlight how these cultures be used to further understand the molecular, cellular, and circuit‐level neuropathophysiological changes underlying stress disorders. BLA OTCs provide long‐term physiological and pharmacological results whose predictions were borne out in vivo, supporting the validity of the BLA OTC as a model to unravel BLA neurocircuitry. Recent preliminary results also support the successful application of this approach to preparing long‐lived OTCs of BLA and neocortex from mice. © 2021 Wiley Periodicals LLC. Basic Protocol 1 : Organotypic slice culture Support Protocol 1 : Changing medium Support Protocol 2 : Drug incubations Basic Protocol 2 : Excision of OTC slices from inserts Support Protocol 3 : Fixation of slices