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Dm400b digital microscope

Manufactured by Leica

The Leica DM400B is a digital microscope designed for high-quality imaging and analysis. It features a high-resolution digital camera and advanced software for capturing and processing images. The DM400B is capable of magnifying samples and providing detailed, accurate information about their structure and composition.

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3 protocols using dm400b digital microscope

1

Brain Tissue Preparation for Microdialysis

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After the microdialysis test session, rats were anesthetized using sodium pentobarbital (270 mg/kg; i.p.) and perfused intracardially with 50 mL of 0.9% saline, followed by 500 mL of 4% paraformaldehyde in 0.1 M phosphate buffer (PB). After being perfused, brains were removed, post-fixed in the same paraformaldehyde solution for 2 hours, then immersed in 20% sucrose and 0.01% sodium azide in 0.1 M PB for 48 hours at 4° C. Coronal sections (40 µm) were cut with a freezing microtome (SM 2000R; Leica), collected in PB, and mounted on to a slide immediately. Sections were imaged at 4x magnification using a Leica DM400B digital microscope to verify cannula placement.
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2

Brain Fixation and Sectioning Protocol

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After the conclusion of the experiment, animals were anesthetized using sodium pentobarbital (270 mg/kg; i.p.) and perfused intracardially with 50 mL of 0.9% saline, followed by 500 mL of 4% paraformaldehyde in 0.1 m phosphate buffer (PB). After being perfused, brains were removed and post-fixed for 1 h at 4 °C in the same fixative, then immersed in 20% sucrose and 0.01% sodium azide in 0.1 m PB and stored at 4 °C. Coronal sections (40 μm) were cut with a freezing microtome (SM 2000R; Leica), collected in three parallel series in cryoprotectant solution (30% sucrose and 30% ethylene glycol in 0.1 m PB) and stored at −20 °C. Cresyl violet-stained sections were imaged at 4× magnification using a Leica DM400B digital microscope to verify probe placement.
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3

Chronic Glutamate Recording in Rodent DMS

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Microelectrode arrays (MEAs) were chronically implanted into the DMS to record extracellular glutamate levels while performing the CTTT. Following the completion of experiments, administration of a lethal dose of sodium pentobarbital (270 mg/kg, i.p.) was followed by transcardial perfusion of saline, followed by 4% paraformaldehyde in 0.15 m sodium-phosphate solution, pH 7.4. Extracted brains were postfixed in 4% paraformaldehyde for 24 hrs, then submerged in 30% sucrose solution until they sank. Using a freezing microtome (CM 2000R; Leica), 35-μm thick brain slices were sectioned and stored in cryoprotectant until further histologic processing. Sections were mounted and processed with a Cresyl Violet Nissl stain to confirm MEAs placement. A Leica DM400B digital microscope was used to photomicrograph the sections at 1.25X and 5X magnification at three A-P levels (0.2 mm, 0.5 mm, and 1.0 mm).
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