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  • Ovid Technologies (Wolters Kluwer Health)  (2)
  • 2015-2019  (2)
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  • Ovid Technologies (Wolters Kluwer Health)  (2)
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  • 2015-2019  (2)
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  • 1
    In: Stroke, Ovid Technologies (Wolters Kluwer Health), Vol. 48, No. 12 ( 2017-12), p. 3375-3383
    Abstract: Striatal GABAergic neuron is known as a key regulator in adult neurogenesis. However, the specific role of striatal GABAergic neuronal activity in the promotion of neurological recovery after ischemic stroke remains unknown. Here, we used optogenetic approach to investigate these effects and mechanism. Methods— Laser stimulation was delivered via an implanted optical fiber to inhibit or activate the striatal GABAergic neurons in Gad2-Arch-GFP or Gad2-ChR2-tdTomato mice (n=80) 1 week after 60-minute transient middle cerebral artery occlusion. Neurological severity score, brain atrophy volume, microvessel density, and cell morphological changes were examined using immunohistochemistry. Gene expression and protein levels of related growth factors were further examined using real-time polymerase chain reaction and Western blotting. Results— Inhibiting striatal GABAergic neuronal activity improved functional recovery, reduced brain atrophy volume, and prohibited cell death compared with the control ( P 〈 0.05). Microvessel density and bFGF (basic fibroblast growth factor) expression in the inhibition group were also increased ( P 〈 0.05). In contrast, activation of striatal GABAergic neurons resulted in adverse effects compared with the control ( P 〈 0.05). Using cocultures of GABAergic neurons, astrocytes, and endothelial cells, we further demonstrated that the photoinhibition of GABAergic neuronal activity could upregulate bFGF expression in endothelial cells, depending on the presence of astrocytes. The conditioned medium from the aforementioned photoinhibited 3-cell coculture system protected cells from oxygen glucose deprivation injury. Conclusions— After ischemic stroke, optogenetic inhibition of GABAergic neurons upregulated bFGF expression by endothelial cells and promoted neurobehavioral recovery, possibly orchestrated by astrocytes. Optogenetically inhibiting neuronal activity provides a novel approach to promote neurological recovery.
    Type of Medium: Online Resource
    ISSN: 0039-2499 , 1524-4628
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2017
    detail.hit.zdb_id: 1467823-8
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  • 2
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2018
    In:  Arteriosclerosis, Thrombosis, and Vascular Biology Vol. 38, No. Suppl_1 ( 2018-05)
    In: Arteriosclerosis, Thrombosis, and Vascular Biology, Ovid Technologies (Wolters Kluwer Health), Vol. 38, No. Suppl_1 ( 2018-05)
    Abstract: Aims: Insulin has been reported to influence cholesterol removal from different cells, but the results have been controversial. Based on our previous study, which we found that insulin promote cholesterol efflux from HepG2 cells and can reverse the decreased cholesterol efflux to HDL though PI3K-Akt pathway, we further investigate the effects of insulin on damaged cholesterol efflux by MCP-1 in this report. Methods: 3T3-L1 preadipocytes were differentiated into adipocytes as described previously. Fully differentiated adipocytes (day 13) were labeled with 3 H-cholesterol (1 Ci/ml) for 24 h. Cellular cholesterol efflux was initiated by 20μg/ml human apoA1 or 50 μg/ml HDL 3 with the indicated dose of MCP-1 for the indicated period of time in the presence or absence of insulin. After incubation, the radioactivity of the medium and cells was measured using a liquid scintillation counter. Cholesterol efflux was calculated as the percentage of total [ 3 H]-cholesterol released into the medium after subtraction of the values obtained in the absence of a cholesterol acceptor. 3T3-L1 adipocytes were harvested for PCR , western blotting, cell-surface protein assays and Confocal microscopy. Results: 1. MCP-1 reduced cholesterol efflux to HDL3 and apoA1 in differentiated 3T3-L1 adipocytes. 2. In differentiated 3T3-L1 adipocytes, MCP-1 reduced cholesterol efflux to HDL 3 mainly by inhibiting SR-BI and ABCG1 and to apoA1 mainly by inhibiting ABCA1. 3. MCP-1 decreased ABCA1 and SR-BI mRNA expression but not ABCG1. 4. MCP-1 decreased total and cell surface ABCA1, ABCG1, and SR-BI protein expression as shown by Western blotting and confocal microscopy in differentiated 3T3-L1 adipocytes. 5. Insulin increased MCP-1 suppressed cholesterol efflux to HDL 3 and apoA1 depending on Akt phosphorylation. 6. Insulin reversed MCP-1 suppressed ABCA1 and SR-BI mRNA expression, and ABCA1, ABCG1 and SR-BI protein expression via PI3K/Akt pathway. Conclusions: Insulin reverses the suppressed cholesterol efflux to HDL3 and apoA1 by MCP-1 through up-regulation of ABCA1, ABCG1 and SR-BI through PI3K/Akt pathway in 3T3-L1 adipocytes, which provides evidences that insulin may improve the MCP-1-induced adipocyte cholesterol imbalance to exert the anti-inflammatory effect.
    Type of Medium: Online Resource
    ISSN: 1079-5642 , 1524-4636
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2018
    detail.hit.zdb_id: 1494427-3
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