Abstract

Korean red pine (Pinus densiflora) belongs to the Genus Pinus, and its bark contains a great amount of naturally occurring phenolic compounds. Until now, few studies have been conducted to assess the neuroprotective effects of Pinus densiflora bark extract against brain ischemic injury. The aim of this study was to investigate the neuroprotective effects of pre-treatment with the extract in the hippocampus following 5-min transient forebrain ischemia in gerbils. Furthermore, this study examined the anti-inflammatory effect as a neuroprotective mechanism of the extract. Pinus densiflora bark was extracted by pure water (100 °C), and this extract was quantitatively analyzed and contained abundant polyphenols, flavonoids, and proanthocyanidins. The extract (25, 50, and 100 mg/kg) was orally administered once a day for seven days before the ischemia. In the gerbil hippocampus, death of the pyramidal neurons was found in the subfield cornu ammonis 1 (CA1) five days after the ischemia. This death was significantly attenuated by pre-treatment with 100 mg/kg, not 25 or 50 mg/kg, of the extract. The treatment with 100 mg/kg of the extract markedly inhibited the activation of microglia (microgliosis) and significantly decreased the expression of pro-inflammatory cytokines (interleukin 1β and tumor necrosis factor α). In addition, the treatment significantly increased anti-inflammatory cytokines (interleukin 4 and interleukin 13). Taken together, this study clearly indicates that pre-treatment with 100 mg/kg of Pinus densiflora bark extract in gerbils can exert neuroprotection against brain ischemic injury by the attenuation of neuroinflammatory responses.

Highlights

  • Transient ischemia in brains occurs when blood supply to the brain is temporarily lost [1]

  • In the Pinus densiflora Bark Extract (PBE) + transient forebrain ischemia (TFI) group, TNF-α cells1(imFI3(niF1gm.iu3tguh%ruenerao4evtrAee24(ahedBc,itfaaci)yv,l)Ces.it)ayI+.nnidsnthh1Ca2emA6.v10e%gphryaoicrtual5empd,+iadIyLTasl-F1pcIβeolgsltisr-moiwsumcahpsue,msnIlLioigar-h1ectoβalymcitpiminvacmrirteeyduasnwweodiatrhseaatffhtoceaturtivnTthidFteIy:isnthihnaCemtARhgI1erwoppuayypsrraammiiddaall cells was dramatically increased (189.3% of the sham group) at 2 days post-ischemia

  • Pycnogenol®, which is a standardized pine bark extract originating from French maritime, shows an excellent neuroprotective effect against brain ischemic injury induced by TFI in gerbils by strong antioxidant efficacy [13]

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Summary

Introduction

Transient ischemia in brains occurs when blood supply to the brain is temporarily lost [1]. The most effective treatment for ischemic brains is to restore blood supply to the brains as soon as possible. When the restoration of blood supply is too late, ischemia-reperfusion injury leads to delayed neuronal death in vulnerable brain structures, such as the hippocampal CA1 [2,3]. Numerous studies have proposed diverse mechanisms of the delayed neuronal death due to ischemia-reperfusion injury, including glutamate-induced excitotoxicity, oxidative stress following excessive generation of reactive oxygen species (ROS), glia-mediated neuroinflammation, and blood-brain barrier (BBB) disruption [4,5,6]. Pine bark extract has been studied to have usable polyphenols, including proanthocyanidins, which display various pharmacological properties [9,10]. Pine bark extract has been traditionally used for various diseases and is utilized for nutritional supplements [11,12]

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