Abstract

Background: Cranial radiotherapy is clinically used in the treatment of brain tumours; however, the consequent cognitive and emotional dysfunctions seriously impair the life quality of patients. LW-AFC, an active fraction combination extracted from classical traditional Chinese medicine prescription Liuwei Dihuang decoction, can improve cognitive and emotional dysfunctions in many animal models; however, the protective effect of LW-AFC on cranial irradiation–induced cognitive and emotional dysfunctions has not been reported. Recent studies indicate that impairment of adult hippocampal neurogenesis (AHN) and alterations of the neurogenic microenvironment in the hippocampus constitute critical factors in cognitive and emotional dysfunctions following cranial irradiation. Here, our research further investigated the potential protective effects and mechanisms of LW-AFC on cranial irradiation–induced cognitive and emotional dysfunctions in mice. Methods: LW-AFC (1.6 g/kg) was intragastrically administered to mice for 14 days before cranial irradiation (7 Gy γ-ray). AHN was examined by quantifying the number of proliferative neural stem cells and immature neurons in the dorsal and ventral hippocampus. The contextual fear conditioning test, open field test, and tail suspension test were used to assess cognitive and emotional functions in mice. To detect the change of the neurogenic microenvironment, colorimetry and multiplex bead analysis were performed to measure the level of oxidative stress, neurotrophic and growth factors, and inflammation in the hippocampus. Results: LW-AFC exerted beneficial effects on the contextual fear memory, anxiety behaviour, and depression behaviour in irradiated mice. Moreover, LW-AFC increased the number of proliferative neural stem cells and immature neurons in the dorsal hippocampus, displaying a regional specificity of neurogenic response. For the neurogenic microenvironment, LW-AFC significantly increased the contents of superoxide dismutase, glutathione peroxidase, glutathione, and catalase and decreased the content of malondialdehyde in the hippocampus of irradiated mice, accompanied by the increase in brain-derived neurotrophic factor, insulin-like growth factor-1, and interleukin-4 content. Together, LW-AFC improved cognitive and emotional dysfunctions, promoted AHN preferentially in the dorsal hippocampus, and ameliorated disturbance in the neurogenic microenvironment in irradiated mice. Conclusion: LW-AFC ameliorates cranial irradiation–induced cognitive and emotional dysfunctions, and the underlying mechanisms are mediated by promoting AHN in the dorsal hippocampus and improving the neurogenic microenvironment. LW-AFC might be a promising therapeutic agent to treat cognitive and emotional dysfunctions in patients receiving cranial radiotherapy.

Highlights

  • People are subjected to irradiation exposure commonly during the process of radiodiagnosis and radiotherapy (Brenner and Hall, 2007; Manda and Reiter, 2010; Hladik and Tapio, 2016)

  • To observe the effects of active fraction combination from Liuwei Dihuang decoction (LW-AFC) pretreatment for 2 weeks on cognitive and emotional dysfunctions induced by cranial irradiation, the contextual fear conditioning, open field, and tail suspension tests were used on the first day after irradiation

  • A significant increase in the time in the center zone was observed in IR mice compared with the control mice, and this change was restored by Liuwei Dihuang decoction (LW)-AFC pretreatment (p < 0.001) (Figure 3B)

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Summary

Introduction

People are subjected to irradiation exposure commonly during the process of radiodiagnosis and radiotherapy (Brenner and Hall, 2007; Manda and Reiter, 2010; Hladik and Tapio, 2016). Cognitive and emotional dysfunctions in patients after treatment with cranial irradiation point to hippocampal damage, and recent evidence indicates that the impairment of adult hippocampal neurogenesis (AHN) is one of the most important mechanisms involved in cranial irradiation–induced cognitive and emotional dysfunctions (Raber et al, 2004; Limoli et al, 2007; Naylor et al, 2008; Acharya et al, 2011). It is reported that the neurogenic microenvironment (neurogenic niche) in the hippocampus modulates the different processes of neural stem cell development and cranial irradiation damages the neurogenic microenvironment, which mainly correlates with the reduced AHN (Monje and Palmer, 2003; Fike et al, 2007; Ming and Song, 2011; Huang T.-T. et al, 2012). Recent studies indicate that impairment of adult hippocampal neurogenesis (AHN) and alterations of the neurogenic microenvironment in the hippocampus constitute critical factors in cognitive and emotional dysfunctions following cranial irradiation. Our research further investigated the potential protective effects and mechanisms of LW-AFC on cranial irradiation–induced cognitive and emotional dysfunctions in mice

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