Chronic Unexpected Mild Stress Destroys Synaptic Plasticity of Neurons through a Glutamate Transporter, GLT-1, of Astrocytes in the Ischemic Stroke Rat

<div>Ceftriaxone promoted newborn astrocytes in hippocampal DG in the CUMS-induced model rats transporting glutamate. (a) Representative immunofluorescent photomicrographs (200×) of glutamate (Glu, green) in newborn astrocytes (GFAP/BrdU, red/blue) were pictured on the 21st/28th/42nd day. Scale bars: 20 <i>μ</i>m. (b) Representative immunofluorescent photomicrographs (200×) of glutamine (Gln, green) in newborn astrocytes (GFAP/BrdU, red/blue) on the 21st/28th/42nd day. Scale bars: 20 <i>μ</i>m. (c) Fluorescence intensity of glutamate in newborn astrocytes was modulated by astroglial GLT-1. 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Neural Plasticity

fig3

Figure 3

Figure 3: Chronic Unexpected Mild Stress Destroys Synaptic Plasticity of Neurons through a Glutamate Transporter, GLT-1, of Astrocytes in the Ischemic Stroke Rat 

Figure 3 | Chronic Unexpected Mild Stress Destroys Synaptic Plasticity of Neurons through a Glutamate Transporter, GLT-1, of Astrocytes in the Ischemic Stroke Rat 