PMID- 23823484 OWN - NLM STAT- MEDLINE DCOM- 20140121 LR - 20131128 IS - 1475-2662 (Electronic) IS - 0007-1145 (Linking) VI - 110 IP - 12 DP - 2013 Dec TI - Disruption of calmodulin-dependent protein kinase II alpha/brain-derived neurotrophic factor (alpha-CaMKII/BDNF) signalling is associated with zinc deficiency-induced impairments in cognitive and synaptic plasticity. PG - 2194-200 LID - 10.1017/S0007114513001657 [doi] AB - Maternal dietary Zn deficiency during fetal development induces substantial cognitive dysfunctions in the resultant offspring. The mechanism underlying this effect is unclear. The present study evaluated whether the impairments caused by gestational and lactational Zn deficiency are mediated by the hippocampal calmodulin-dependent protein kinase II alpha (alpha-CaMKII)/brain-derived neurotrophic factor (BDNF) signalling pathway as well as whether they can be restored by postnatal Zn supplementation. Rats were randomly divided into four groups on the first day of pregnancy (n 12): control (CO) group; pair-fed (PF) group; Zn-deprived (ZD) group; orally Zn-supplemented group. The spatial memory of the offspring was tested at postnatal day 35 using the Morris water maze. Long-term potentiation (LTP) in the rat hippocampal medial perforant path-dentate gyrus pathway was evaluated simultaneously, and alpha-CaMKII and BDNF protein levels were examined by Western blot analysis. The results demonstrated that the ZD group exhibited a significantly longer latency period in the Morris water maze as well as a significantly decreased LTP amplitude compared with the CO and PF groups. alpha-CaMKII and BDNF protein expression in the hippocampus was significantly reduced in the ZD group. Postnatal Zn supplementation restored the cognitive dysfunction induced by gestational Zn deficiency but could not completely reverse the decreased LTP and alpha-CaMKII/BDNF protein levels. Our findings suggest that the alpha-CaMKII/BDNF signalling pathway may be involved in Zn deficiency-induced cognitive and synaptic impairments. FAU - Yu, XiaoDan AU - Yu X AD - MOE-Shanghai Key Laboratory of Children's Environmental Health, XinHua Hospital, Shanghai Jiao Tong University School of Medicine, 1665 Kong Jiang Road, Shanghai 200092, People's Republic of China. FAU - Ren, Tianhong AU - Ren T FAU - Yu, XiaoGang AU - Yu X LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130703 PL - England TA - Br J Nutr JT - The British journal of nutrition JID - 0372547 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Trace Elements) RN - EC 2.7.11.17 (Calcium-Calmodulin-Dependent Protein Kinase Type 2) RN - J41CSQ7QDS (Zinc) SB - IM MH - Animals MH - Animals, Newborn MH - Brain-Derived Neurotrophic Factor/*metabolism MH - Calcium-Calmodulin-Dependent Protein Kinase Type 2/*metabolism MH - Cognition Disorders/drug therapy/*etiology/metabolism/physiopathology MH - Deficiency Diseases/*complications/drug therapy/metabolism/physiopathology MH - *Dietary Supplements MH - Female MH - Hippocampus/drug effects/*physiopathology MH - Lactation MH - Male MH - Maze Learning MH - Memory Disorders/drug therapy/etiology/metabolism/physiopathology MH - Neuronal Plasticity/drug effects MH - Pregnancy MH - Prenatal Nutritional Physiological Phenomena MH - Rats MH - Rats, Sprague-Dawley MH - Signal Transduction MH - Trace Elements/deficiency/therapeutic use MH - Zinc/*deficiency/therapeutic use EDAT- 2013/07/05 06:00 MHDA- 2014/01/22 06:00 CRDT- 2013/07/05 06:00 PHST- 2013/07/05 06:00 [entrez] PHST- 2013/07/05 06:00 [pubmed] PHST- 2014/01/22 06:00 [medline] AID - S0007114513001657 [pii] AID - 10.1017/S0007114513001657 [doi] PST - ppublish SO - Br J Nutr. 2013 Dec;110(12):2194-200. doi: 10.1017/S0007114513001657. Epub 2013 Jul 3.