» Articles » PMID: 25023312

Acute Brain Slice Methods for Adult and Aging Animals: Application of Targeted Patch Clamp Analysis and Optogenetics

Overview
Specialty Molecular Biology
Date 2014 Jul 16
PMID 25023312
Citations 352
Authors
Affiliations
Soon will be listed here.
Abstract

The development of the living acute brain slice preparation for analyzing synaptic function roughly a half century ago was a pivotal achievement that greatly influenced the landscape of modern neuroscience. Indeed, many neuroscientists regard brain slices as the gold-standard model system for detailed cellular, molecular, and circuitry level analysis and perturbation of neuronal function. A critical limitation of this model system is the difficulty in preparing slices from adult and aging animals, and over the past several decades few substantial methodological improvements have emerged to facilitate patch clamp analysis in the mature adult stage. In this chapter we describe a robust and practical protocol for preparing brain slices from mature adult mice that are suitable for patch clamp analysis. This method reduces swelling and damage in superficial layers of the slices and improves the success rate for targeted patch clamp recordings, including recordings from fluorescently labeled populations in slices derived from transgenic mice. This adult brain slice method is suitable for diverse experimental applications, including both monitoring and manipulating neuronal activity with genetically encoded calcium indicators and optogenetic actuators, respectively. We describe the application of this adult brain slice platform and associated methods for screening kinetic properties of Channelrhodopsin (ChR) variants expressed in genetically defined neuronal subtypes.

Citing Articles

Untangling dopamine and glutamate in the ventral tegmental area.

Prevost E, Ward L, Alas D, Aimale G, Ikenberry S, Fox K bioRxiv. 2025; .

PMID: 40060543 PMC: 11888473. DOI: 10.1101/2025.02.25.640201.


Rodent islet amyloid polypeptide (IAPP) selectively enhances GABA receptor-mediated neuronal inhibition in mouse ventral but not dorsal hippocampal dentate gyrus granule cells.

Netsyk O, Korol S, Westermark G, Birnir B, Jin Z Front Cell Neurosci. 2025; 19:1531790.

PMID: 40046847 PMC: 11880208. DOI: 10.3389/fncel.2025.1531790.


Retinal and thalamic alterations in the 5xFAD mouse model of Alzheimer's disease.

McCool S, Smith J, Sladek A, Fan S, Van Hook M PLoS One. 2025; 20(3):e0319397.

PMID: 40029927 PMC: 11875347. DOI: 10.1371/journal.pone.0319397.


An endogenous GLP-1 circuit engages VTA GABA neurons to regulate mesolimbic dopamine neurons and attenuate cocaine seeking.

Merkel R, Hernandez N, Weir V, Zhang Y, Caffrey A, Rich M Sci Adv. 2025; 11(9):eadr5051.

PMID: 40009667 PMC: 11864183. DOI: 10.1126/sciadv.adr5051.


CHOLINERGIC MODULATION OF CELLULAR RESONANCE IN NON-HUMAN PRIMATE HIPPOCAMPUS.

Gambrill A, Rueckemann J, Barria A bioRxiv. 2025; .

PMID: 39829940 PMC: 11741476. DOI: 10.1101/2025.01.10.632495.


References
1.
Brahma B, Forman R, Stewart E, Nicholson C, Rice M . Ascorbate inhibits edema in brain slices. J Neurochem. 2000; 74(3):1263-70. DOI: 10.1046/j.1471-4159.2000.741263.x. View

2.
Hille B . The permeability of the sodium channel to organic cations in myelinated nerve. J Gen Physiol. 1971; 58(6):599-619. PMC: 2226049. DOI: 10.1085/jgp.58.6.599. View

3.
Chen Q, Cichon J, Wang W, Qiu L, Lee S, Campbell N . Imaging neural activity using Thy1-GCaMP transgenic mice. Neuron. 2012; 76(2):297-308. PMC: 4059513. DOI: 10.1016/j.neuron.2012.07.011. View

4.
Huang S, Uusisaari M . Physiological temperature during brain slicing enhances the quality of acute slice preparations. Front Cell Neurosci. 2013; 7:48. PMC: 3632751. DOI: 10.3389/fncel.2013.00048. View

5.
Mainen Z, Maletic-Savatic M, Shi S, Hayashi Y, Malinow R, Svoboda K . Two-photon imaging in living brain slices. Methods. 1999; 18(2):231-9, 181. DOI: 10.1006/meth.1999.0776. View