Publications by authors named "Linna Pan"

Background: It has been shown that chronic stress-induced depression is associated with exaggerated inflammatory response in the brain. Alpha7 nicotinic acetylcholine receptors (α7nAChRs) regulate the cholinergic anti-inflammatory pathway, but the role of cholinergic signaling and α7nAChR in chronic stress has not yet been examined.

Methods: In this study, we used a well-documented model of depression in which mice were exposed to 6 h of restraint stress for 21 consecutive days.

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Aims: Brain ischemia activates astrocytes in a process known as astrogliosis. Although this process has beneficial effects, excessive astrogliosis can impair neuronal recovery. Polyinosinic-polycytidylic acid (Poly IC) has shown neuroprotection against cerebral ischemia-reperfusion injury, but whether it regulates reactive astrogliosis and glial scar formation is not clear.

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Background: Cerebral ischemic preconditioning (IPC) protects brain against ischemic injury. Activation of Toll-like receptor 3 (TLR3) signaling can induce neuroprotective mediators, but whether astrocytic TLR3 signaling is involved in IPC-induced ischemic tolerance is not known.

Methods: IPC was modeled in mice with three brief episodes of bilateral carotid occlusion.

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Geraniin has previously been reported to possess extensive biological activity. In this study, we reported that geraniin is an inhibitor of tumor activity in vitro and in vivo. Geraniin suppressed the proliferation of A549 cells in a dose- and time-dependent manner.

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Article Synopsis
  • The study investigates how the TLR3 agonist Poly I:C provides neuroprotection in acute ischemic conditions using both in vitro (astrocyte cultures) and in vivo (mouse models) approaches.
  • Poly I:C treatment before simulated ischemia significantly improves cell viability, decreases cell damage, and reduces inflammation indicators like TNFα and IL-6.
  • The findings suggest that the neuroprotective effects of Poly I:C are linked to the activation of the TLR3-TRIF signaling pathway, highlighting its potential as a therapeutic strategy for ischemic brain injuries.
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