Environmental Stimulation Counteracts the Suppressive Effects of Maternal High-Fructose Diet on Cell Proliferation and Neuronal Differentiation in the Dentate Gyrus of Adult Female Offspring via Histone Deacetylase 4

• Published in: International journal of environmental research and public health Vol. 17; no. 11; p. 3919
• Main Authors: Liu, Wen-Chung, Wu, Chih-Wei, Hung, Pi-Lien, Chan, Julie Y. H., Tain, You-Lin, Fu, Mu-Hui, Chen, Lee-Wei, Liang, Chih-Kuang, Hung, Chun-Ying, Yu, Hong-Ren, Chen, I-Chun, Wu, Kay L.H.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.06.2020; MDPI
• Subjects: Brain-derived neurotrophic factor; Breastfeeding & lactation; Cell differentiation; Cell proliferation; Dentate gyrus; Diet; Differentiation; Doublecortin protein; Enrichment; Environmental effects; Enzymatic activity; Enzyme activity; Fructose; Gene expression; Hippocampus; Histone deacetylase; Histones; Laboratory animals; Memory; Neural networks; Neural stem cells; Neurogenesis; Neurons; Offspring; Pax6 protein; Proteins; Stem cells; Stimulation; Toys; Transcription factors; Weaning; United States > US; Taiwan
• ISSN: 1660-4601; 1661-7827; 1660-4601
• DOI: 10.3390/ijerph17113919

Maternal high-fructose diets (HFD) impair the learning and memory capacity of adult female offspring via histone deacetylase 4 (HDAC4). Hippocampal adult neurogenesis is important for supporting the function of existing neural circuits. In this study, we investigated the effects of maternal HFD on hippocampal neural stem cell (NSC) proliferation and neuronal differentiation in adult offspring. Increased nuclear HDAC4 enzyme activity was detected in the hippocampus of HFD female offspring. The Western blot analyses indicated that the expressions of sex-determining region Y box2 (SOX2) and the transcription factor Paired Box 6 (PAX6), which are critical for the progression of NSC proliferation and differentiation, were downregulated. Concurrently, the expression of Ki67 (a cellular marker for proliferation) and doublecortin (DCX), which are related to NSC division and neuronal differentiation, was suppressed. Intracerebroventricular infusion with class II HDAC inhibitor (Mc1568, 4 weeks) led to the upregulation of these proteins. Environmental stimulation reversed the expression of Ki67 and DCX and the counts of Ki67- and DCX-positive cells in the hippocampi of HFD offspring as a result of providing the enriched housing for 4 weeks. Together, these results demonstrate that the suppressive effects of maternal HFD on hippocampal NSC proliferation and neuronal differentiation are reversibly mediated through HDAC4 and can be effectively reversed by environmental stimulation. The advantageous effects of environmental enrichment were possibly mediated by HDAC4 suppression.