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The purpose of this protocol is to describe a method to produce slices of the dorsal hippocampus for electrophysiological examination. This procedure employs perfusion with chilled ACSF prior to slice preparation with a near-coronal slicing angle which allows for preservation of healthy principal neurons.
Whole-cell patch-clamp recordings from acute rodent brain slices are a mainstay of modern neurophysiological research, allowing precise measurement of cellular and synaptic properties. Nevertheless, there is an ever increasing need to perform correlated analyses between different experimental modes in addition to slice electrophysiology, for example: immunohistochemistry, molecular biology, in vivo imaging or electrophysiological recording; to answer evermore complex questions of brain function. However, making meaningful conclusions from these various experimental approaches is not straightforward, as even within relatively well described brain structures, a high degree of sub-regional variation of cellular function exists. Nowhere is this better exemplified than in the CA1 of the hippocampus, which has well-defined dorso-ventral properties, based on cellular and molecular properties. Nevertheless, many published studies examine protein expression patterns or behaviorally correlated in vivo activity in the dorsal extent of the hippocampus; and explain findings mechanistically with cellular electrophysiology from the ventro-medial region. This is further confounded by the fact that many acute slice electrophysiological experiments are performed in juvenile animals, when other experimental modes are performed in more mature animals. To address these issues, this method incorporates transcardial perfusion of mature (>60 day old rodents) with artificial cerebrospinal fluid followed by preparation of modified coronal slices including the septal pole of the dorsal hippocampus to record from CA1 pyramidal cells. This process leads to the generation of healthy acute slices of dorsal hippocampus allowing for slice-based cellular electrophysiological interrogation matched to other measures.
The hippocampus is arguably the most well studied structure in the mammalian brain, due to its relatively large size and prominent laminar structure. The hippocampus has been implicated in a number of behavioral processes: spatial navigation, contextual memory, and episode formation. This is, in part, due to the relative ease of access to the dorsal portions of the hippocampus in rodents for in vivo analysis. Indeed, the major output cells are typically less than 2 mm from the pial surface.
In rodents, the hippocampus is a relatively large structure, formed of an invagination of the telencephalon extending from the dorsal septum to....
All animals were generated and maintained according to the Home Office and Institutional guidelines (HO# P135148E). All rats were maintained on a 12 h light/dark cycle and given ad libitum access to food and water.
1. Transcardial perfusion of chilled ACSF
The protocol described above allows for the preparation of viable slices from the septal pole of the dorsal hippocampus in mature rats. A key factor in this protocol is the perfusion of chilled sucrose-ACSF, prior to slice preparation, resulting in healthy CA1 PCs proximal to the slice surface. The quality of the slice produced is assessed visually under IR-DIC optics, and healthy cells identified as having large, ovoid-shaped cell bodies are located throughout the full extent of stratum pyramidale, from the com.......
Here, a protocol is described to produce high-quality brain slices from the dorsal extent of the CA1 of the hippocampus, allowing for recordings from multiple viable neurons within this region. The combinatorial approach of whole-cell recording from near-coronal slices followed by neuron visualization is critical to the confirmation of cell viability and identity.
This protocol reliably produces viable slices for 2 major reasons. Firstly, the modification to the cutting angle, as a deviation f.......
The author wishes to thank Prof. David JA Wyllie, Dr. Emma Perkins, Laura Simoes de Oliveira, and Prof. Peter C Kind for helpful comments on the manuscript and protocol optimisation, and The Simons Initiative for the Developing Brain for providing publication costs.
....Name | Company | Catalog Number | Comments |
Acquisition software | Molecular Devices | pClamp 10 | |
Adult rats | Various | n/a | Any strain of adult rat (60 days and older) |
Amplifier | Molecular Devices | Axopatch 700B | |
Analysis software | Freeware | Stimfit | https://github.com/neurodroid/stimfit |
Bone Scissors | FST | 16152-12 | Littauer style |
Capillary Glass | Harvard Apparatus | 30-0060 | Borosilicate glass pipettes with filament 1.5 mm outer diameter, 0.86 mm inner diameter. |
Carbogen | BOC | Various | 95% O2/5% CO2 |
CCD camera | Scientifica | SciCamPro | https://www.scientifica.uk.com/products/ |
Chemicals/Reagents | Sigma Aldrich | Various | All laboratory reagents procured from Sigma Aldrich. |
Cyanoacrylate (i.e. RS Pro 3) | RS Components | 918-6872 | Avoid gel based cyanoacrylate formulations |
Digitizer | Molecular Devices | Digidata 1550B | |
Dissection pins/needles | Various | Various | Use 16 gauge needles (above) |
Electrophysiology system | Scientifica | SliceScope | https://www.scientifica.uk.com/products/ scientifica-slicescope |
Fine iris scissors | FST | 14568-12 | With Tungsten-Carbide tips |
Glass Petri dish | Fisher Scientific | 12911408 | |
Hypodermic needles | BD Healthcare | Various | 16, 18, and 22 gauge |
Isofluorane 100% W/W (i.e.IsoFlo) | Zoetis | 50019100 | |
Mayo-type scissors | FST | 14110-17 | Blunt tips |
Micromanipulators | Scientifica | Microstar | https://www.scientifica.uk.com/products/scientifica-microstar-micromanipulator |
Paintbrush | Art store | n/a | A fine bristled paintbrush, procured from a local art shop. |
Pasteur pipette | Fisher Scientific | 11546963 | A glass Pasteur pipette, but cut so that the blunt end is used to transfer pipette. |
Peristaltic pump | Watson Marlow | 12466260 | Single channel peristaltic pump |
Pipette puller | Sutter Instruments | P-97 | Other models and methods of pipette production would work equally well. |
Plastic syringes (1, 2, 5 mL) | BD Healthcare | Various | |
Rongeur bone tool | FST | 16021-14 | |
Slice holding chamber | Homemade | ||
Slice weight/harp | Harvard Apparatus | SHD-22L/15 | Alternatives would be suitable. |
Sodium Pentobarbital (i.e. Pentoject) | Animalcare Ltd | 10347/4014 | 200 mg/mL; other formulations of pentobarbital would be suitable |
Spatula | Bochem | 3213 | Available from Fisher Scientific |
Syringe filters | Fisher Scientific | 10482012 | Corning brand syringe filters, 0.22 µm pore diameter. |
Vibtratome | Leica | 1491200S001 | VT1200S model with Vibrocheck |
Water Bath | Fisher Scientific | 15167015 | 5 Litre water bath, for example: Grant Instrumentsâ„¢JBA5 scientifica-scicam-pro |
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