Activation of GABAB2 subunits alleviates chronic cerebral hypoperfusion-induced anxiety-like behaviours: A role for BDNF signalling and Kir3 channels. (November 2016)
- Record Type:
- Journal Article
- Title:
- Activation of GABAB2 subunits alleviates chronic cerebral hypoperfusion-induced anxiety-like behaviours: A role for BDNF signalling and Kir3 channels. (November 2016)
- Main Title:
- Activation of GABAB2 subunits alleviates chronic cerebral hypoperfusion-induced anxiety-like behaviours: A role for BDNF signalling and Kir3 channels
- Authors:
- Lu, Yun
Li, Chang-jun
Chen, Cheng
Luo, Pan
Zhou, Mei
Li, Cai
Xu, Xu-lin
Lu, Qing
He, Zhi
Guo, Lian-jun - Abstract:
- Abstract: Anxiety is an affective disorder that is commonly observed after irreversible brain damage induced by cerebral ischemia and can delay the physical and cognitive recovery, which affects the quality of life of both the patient and family members. However, anxiety after ischemia has received less attention, and mechanisms underlying anxiety-like behaviours induced by chronic cerebral ischemia are under-investigated. In the present study, the chronic cerebral hypoperfusion model was established by the permanent occlusion of the bilateral common carotid arteries (two-vessel occlusion, 2VO) in rats, and anxiety-related behaviours were evaluated. Results indicated that 2VO induced obvious anxiety-like behaviours; the surface expressions of GABAB2 subunits were down-regulated; Brain derived neurotrophic factor (BDNF), tyrosine kinase B (TrkB) and neural cell adhesion molecule (NCAM) were reduced; Meanwhile, the surface expressions of G protein-activated inwardly rectifying potassium (GIRK, Kir3) channels were up-regulated in hippocampal CA1 in 2VO rats. Baclofen, a GABAB receptor agonist, significantly ameliorated the anxiety-like behaviours. It also improved the down-regulation of GABAB2 surface expressions, restored the levels of BDNF, TrkB and NCAM, and reversed the increased surface expressions of Kir3 in hippocampal CA1 in 2VO rats. However, the effects of baclofen were absent in shRNA-GABAB2 infected 2VO rats. These results suggested that activation of GABAB2Abstract: Anxiety is an affective disorder that is commonly observed after irreversible brain damage induced by cerebral ischemia and can delay the physical and cognitive recovery, which affects the quality of life of both the patient and family members. However, anxiety after ischemia has received less attention, and mechanisms underlying anxiety-like behaviours induced by chronic cerebral ischemia are under-investigated. In the present study, the chronic cerebral hypoperfusion model was established by the permanent occlusion of the bilateral common carotid arteries (two-vessel occlusion, 2VO) in rats, and anxiety-related behaviours were evaluated. Results indicated that 2VO induced obvious anxiety-like behaviours; the surface expressions of GABAB2 subunits were down-regulated; Brain derived neurotrophic factor (BDNF), tyrosine kinase B (TrkB) and neural cell adhesion molecule (NCAM) were reduced; Meanwhile, the surface expressions of G protein-activated inwardly rectifying potassium (GIRK, Kir3) channels were up-regulated in hippocampal CA1 in 2VO rats. Baclofen, a GABAB receptor agonist, significantly ameliorated the anxiety-like behaviours. It also improved the down-regulation of GABAB2 surface expressions, restored the levels of BDNF, TrkB and NCAM, and reversed the increased surface expressions of Kir3 in hippocampal CA1 in 2VO rats. However, the effects of baclofen were absent in shRNA-GABAB2 infected 2VO rats. These results suggested that activation of GABAB2 subunits could improve BDNF signalling and reverse Kir3 channel surface expressions in hippocampal CA1, which may alleviate the anxiety-like behaviours in rats with chronic cerebral hypoperfusion. Highlights: Chronic cerebral hypoperfusion could induce anxiety-like behaviours in rats. Activation of GABAB2 subunits could alleviate the anxiety-like behaviours. Activation of GABAB2 subunits could improve BDNF signalling in 2VO rats. Activation of GABAB2 subunits could reverse Kir3 surface expression in 2VO rats. … (more)
- Is Part Of:
- Neuropharmacology. Volume 110(2016) Part A
- Journal:
- Neuropharmacology
- Issue:
- Volume 110(2016) Part A
- Issue Display:
- Volume 110, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 110
- Issue:
- 2016
- Issue Sort Value:
- 2016-0110-2016-0000
- Page Start:
- 308
- Page End:
- 321
- Publication Date:
- 2016-11
- Subjects:
- Anxiety-like behaviour -- Chronic cerebral hypoperfusion -- GABAB2 subunit -- BDNF/TrkB/NCAM -- Kir3 channels
2VO two-vessel occlusion -- GABAB γ-aminobutyric acid type B -- CA1 Cornu ammonis 1 -- MWM Morris water maze test -- NOR novel object recognition test -- OFT open field test -- SBI social behaviour interaction -- LTP long-term potentiation -- fEPSP field excitatory postsynaptic potential -- I/O curves input/output curves -- Kir3 G protein-activated inwardly rectifying potassium, GIRK -- BDNF brain derived neurotrophic factor -- TrkB Tyrosine kinase B -- NCAM neural cell adhesion molecule -- SNX27 Sorting nexin 27 -- ZO-2 zonula occludens-2
Neuropsychopharmacology -- Periodicals
Autonomic Agents -- Periodicals
Neuropsychopharmacologie -- Périodiques
Neuropsychopharmacology
Periodicals
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615.78 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00283908 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuropharm.2016.08.007 ↗
- Languages:
- English
- ISSNs:
- 0028-3908
- Deposit Type:
- Legaldeposit
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