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对氨基水杨酸钠通过恢复基底神经节的超微结构改变和γ-氨基丁酸代谢失衡改善锰诱导的学习和记忆功能障碍。

Sodium P-Aminosalicylic Acid Improved Manganese-Induced Learning and Memory Dysfunction via Restoring the Ultrastructural Alterations and γ-Aminobutyric Acid Metabolism Imbalance in the Basal Ganglia.

作者信息

Ou Chao-Yan, Luo Yi-Ni, He Sheng-Nan, Deng Xiang-Fa, Luo Hai-Lan, Yuan Zong-Xiang, Meng Hao-Yang, Mo Yu-Huan, Li Shao-Jun, Jiang Yue-Ming

机构信息

Department of Toxicology, School of Public Health, Guangxi Medical University, 22 Shuang-yong Rd, Nanning, Guangxi, 530021, China.

Department of Toxicology, School of Public Health, Guilin Medical University, Guilin, 541004, China.

出版信息

Biol Trace Elem Res. 2017 Mar;176(1):143-153. doi: 10.1007/s12011-016-0802-4. Epub 2016 Aug 5.

Abstract

Excessive intake of manganese (Mn) may cause neurotoxicity. Sodium para-aminosalicylic acid (PAS-Na) has been used successfully in the treatment of Mn-induced neurotoxicity. The γ-aminobutyric acid (GABA) is related with learning and memory abilities. However, the mechanism of PAS-Na on improving Mn-induced behavioral deficits is unclear. The current study was aimed to investigate the effects of PAS-Na on Mn-induced behavioral deficits and the involvement of ultrastructural alterations and γ-aminobutyric acid (GABA) metabolism in the basal ganglia of rats. Sprague-Dawley rats received daily intraperitoneally injections of 15 mg/kg MnCl.4HO, 5d/week for 4 weeks, followed by a daily back subcutaneously (sc.) dose of PAS-Na (100 and 200 mg/kg), 5 days/week for another 3 or 6 weeks. Mn exposure for 4 weeks and then ceased Mn exposure for 3 or 6 weeks impaired spatial learning and memory abilities, and these effects were long-lasting. Moreover, Mn exposure caused ultrastructural alterations in the basal ganglia expressed as swollen neuronal with increasing the electron density in the protrusions structure and fuzzed the interval of neuropil, together with swollen, focal hyperplasia, and hypertrophy of astrocytes. Additionally, the results also indicated that Mn exposure increased Glu/GABA values as by feedback loops controlling GAT-1, GABA mRNA and GABA protein expression through decreasing GABA transporter 1(GAT-1) and GABA A receptor (GABA) mRNA expression, and increasing GABA protein expression in the basal ganglia. But Mn exposure had no effects on GAT-1 protein expression. PAS-Na treatment for 3 or 6 weeks effectively restored the above-mentioned adverse effects induced by Mn. In conclusion, these findings suggest the involvement of GABA metabolism and ultrastructural alterations of basal ganglia in PAS-Na's protective effects on the spatial learning and memory abilities.

摘要

过量摄入锰(Mn)可能会导致神经毒性。对氨基水杨酸钠(PAS-Na)已成功用于治疗锰诱导的神经毒性。γ-氨基丁酸(GABA)与学习和记忆能力有关。然而,PAS-Na改善锰诱导的行为缺陷的机制尚不清楚。当前的研究旨在探讨PAS-Na对锰诱导的行为缺陷的影响以及大鼠基底神经节中超微结构改变和γ-氨基丁酸(GABA)代谢的参与情况。将Sprague-Dawley大鼠每天腹腔注射15 mg/kg MnCl₂·4H₂O,每周5天,共4周,随后每天皮下注射PAS-Na(100和200 mg/kg),每周5天,再持续3或6周。锰暴露4周后停止锰暴露3或6周会损害空间学习和记忆能力,且这些影响是持久的。此外,锰暴露导致基底神经节超微结构改变,表现为神经元肿胀,突起结构中的电子密度增加,神经毡间隙模糊,同时伴有星形胶质细胞肿胀、局灶性增生和肥大。此外,结果还表明,锰暴露通过控制GAT-1、GABA mRNA和GABA蛋白表达的反馈回路,降低基底神经节中GABA转运体1(GAT-1)和GABA A受体(GABA)mRNA表达,并增加GABA蛋白表达,从而增加Glu/GABA值。但锰暴露对GAT-1蛋白表达没有影响。PAS-Na治疗3或6周有效恢复了锰诱导的上述不良反应。总之,这些发现表明GABA代谢和基底神经节的超微结构改变参与了PAS-Na对空间学习和记忆能力的保护作用。

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