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We are analyzing https://link.springer.com/article/10.1007/s00417-014-2727-y.

Title:
Early spatiotemporal characterization of microglial activation in the retinas of rats with streptozotocin-induced diabetes | Graefe's Archive for Clinical and Experimental Ophthalmology
Description:
Background Microglial activation has been recognized as a neuropathological feature in diabetic retinopathy. But the early spatiotemporal characterization of microglial activation in the retina and the optic nerve of diabetic animals has not been fully investigated. The purpose of this study was to investigate early sequential changes of microglia in the retinas of rats with streptozotocin-induced diabetes. Microglia in the optic nerves of rats with streptozotocin-induced diabetes were also studied. Methods In 4-week, 8-week, and 12-week diabetic and normal control rats, microglial activation in the retinas and optic nerves was evaluated by immunolabeling with OX-42 antibody. Density, proportion of activation, and laminar distribution of retinal microglia were quantified. The retinal mRNA level of Iba-1, a microglial-specific marker, was measured by real-time PCR. Results The density of retinal microglia was not different between diabetic and control rats, but the proportion of activated microglia increased significantly in diabetic rats at each time point. The proportion of microglia increased obviously in the nerve fiber layer and the ganglion cell layer while decreasing in the inner plexiform layer in 12-week diabetic rats. Moreover, retinal Iba-1 mRNA expression increased in 8-week and 12-week diabetic rats. Processes of microglia in the optic nerves of control rats were aligned with the long axis of nerve fibers, while the alignment was disturbed in diabetic rats. Conclusions Morphology, proportion of activation, distribution, and mRNA expression of retinal microglia changed characteristically with the progression of the disease in early-stage diabetic rats.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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  • Education
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Custom-built

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๐ŸŒ  Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {๐Ÿ”}

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Topics {โœ’๏ธ}

month download article/chapter nuclear factor-kappab p65 delta-notch signalling cascades src/akt/cofilin signalling mitogen-activated protein kinase retinal ischemia-reperfusion injury microglia-derived protection streptozotocin-induced diabetic rats early-stage diabetic rats full article pdf experimental ophthalmology aims related subjects versatile effector cells streptozotocin-induced diabetes privacy choices/manage cookies early spatiotemporal characterization minocycline inhibits caspase-1 peripheral nerve grafts nerve fiber layer inhibiting microglia phagocytosis retinal mrna level tumour necrosis factor human diabetic retinopathy proliferative diabetic retinopathy bloodโ€“retinal barrier endotoxin-induced uveitis alleviate vascular phosphatidylinositol-3-kinase/akt ganglion cell layer exacerbated glial response retinal microglial activation article chen minocycline alleviates death optic nerve check access instant access spinal cord injury article graefe' european economic area partial sight certifications aged mouse hippocampus amadori-glycated albumin molecular mechanisms responsible neural cell death microglia release activators microglial-specific marker investigate early sequential conditions privacy policy interleukin-6 mrna expression real-time pcr

Schema {๐Ÿ—บ๏ธ}

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         headline:Early spatiotemporal characterization of microglial activation in the retinas of rats with streptozotocin-induced diabetes
         description:Microglial activation has been recognized as a neuropathological feature in diabetic retinopathy. But the early spatiotemporal characterization of microglial activation in the retina and the optic nerve of diabetic animals has not been fully investigated. The purpose of this study was to investigate early sequential changes of microglia in the retinas of rats with streptozotocin-induced diabetes. Microglia in the optic nerves of rats with streptozotocin-induced diabetes were also studied. In 4-week, 8-week, and 12-week diabetic and normal control rats, microglial activation in the retinas and optic nerves was evaluated by immunolabeling with OX-42 antibody. Density, proportion of activation, and laminar distribution of retinal microglia were quantified. The retinal mRNA level of Iba-1, a microglial-specific marker, was measured by real-time PCR. The density of retinal microglia was not different between diabetic and control rats, but the proportion of activated microglia increased significantly in diabetic rats at each time point. The proportion of microglia increased obviously in the nerve fiber layer and the ganglion cell layer while decreasing in the inner plexiform layer in 12-week diabetic rats. Moreover, retinal Iba-1 mRNA expression increased in 8-week and 12-week diabetic rats. Processes of microglia in the optic nerves of control rats were aligned with the long axis of nerve fibers, while the alignment was disturbed in diabetic rats. Morphology, proportion of activation, distribution, and mRNA expression of retinal microglia changed characteristically with the progression of the disease in early-stage diabetic rats.
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      headline:Early spatiotemporal characterization of microglial activation in the retinas of rats with streptozotocin-induced diabetes
      description:Microglial activation has been recognized as a neuropathological feature in diabetic retinopathy. But the early spatiotemporal characterization of microglial activation in the retina and the optic nerve of diabetic animals has not been fully investigated. The purpose of this study was to investigate early sequential changes of microglia in the retinas of rats with streptozotocin-induced diabetes. Microglia in the optic nerves of rats with streptozotocin-induced diabetes were also studied. In 4-week, 8-week, and 12-week diabetic and normal control rats, microglial activation in the retinas and optic nerves was evaluated by immunolabeling with OX-42 antibody. Density, proportion of activation, and laminar distribution of retinal microglia were quantified. The retinal mRNA level of Iba-1, a microglial-specific marker, was measured by real-time PCR. The density of retinal microglia was not different between diabetic and control rats, but the proportion of activated microglia increased significantly in diabetic rats at each time point. The proportion of microglia increased obviously in the nerve fiber layer and the ganglion cell layer while decreasing in the inner plexiform layer in 12-week diabetic rats. Moreover, retinal Iba-1 mRNA expression increased in 8-week and 12-week diabetic rats. Processes of microglia in the optic nerves of control rats were aligned with the long axis of nerve fibers, while the alignment was disturbed in diabetic rats. Morphology, proportion of activation, distribution, and mRNA expression of retinal microglia changed characteristically with the progression of the disease in early-stage diabetic rats.
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