Neuroprotective Effect of Paeonol Mediates Anti-Inflammation via Suppressing Toll-Like Receptor 2 and Toll-Like Receptor 4 Signaling Pathways in Cerebral Ischemia-Reperfusion Injured Rats.
Wen-Yen LiaoTung-Hu TsaiTin-Yun HoYi-Wen LinChin-Yi ChengChing-Liang HsiehPublished in: Evidence-based complementary and alternative medicine : eCAM (2016)
Paeonol is a phenolic compound derived from Paeonia suffruticosa Andrews (MC) and P. lactiflora Pall (PL). Paeonol can reduce cerebral infarction volume and improve neurological deficits through antioxidative and anti-inflammatory effects. However, the anti-inflammatory pathway of paeonol remains unclear. This study investigated the relationship between anti-inflammatory responses of paeonol and signaling pathways of TLR2 and TLR4 in cerebral infarct. We established the cerebral ischemia-reperfusion model in Sprague Dawley rats by occluding right middle cerebral artery for 60 min, followed by reperfusion for 24 h. The neurological deficit score was examined, and the brains of the rats were removed for cerebral infarction volume and immunohistochemistry (IHC) analysis. The infarction volume and neurological deficits were lower in the paeonol group (pretreatment with paeonol; 20 mg/kg i.p.) than in the control group (without paeonol treatment). The IHC analysis revealed that the number of TLR2-, TLR4-, Iba1-, NF-κB- (P50-), and IL-1β-immunoreactive cells and TUNEL-positive cells was significantly lower in the paeonol group; however, the number of TNF-α-immunoreactive cells did not differ between the paeonol and control groups. The paeonol reveals some neuroprotective effects in the model of ischemia, which could be due to the reduction of many proinflammatory receptors/mediators, although the mechanisms are not clear.
Keyphrases
- toll like receptor
- nuclear factor
- inflammatory response
- induced apoptosis
- signaling pathway
- immune response
- cerebral ischemia
- cell cycle arrest
- middle cerebral artery
- pi k akt
- acute myocardial infarction
- subarachnoid hemorrhage
- oxidative stress
- traumatic brain injury
- heart failure
- endoplasmic reticulum stress
- coronary artery disease
- rheumatoid arthritis
- lps induced
- acute coronary syndrome
- internal carotid artery
- cerebral blood flow