Sentürk U K, Oner G
Akdeniz University, Faculty of Medicine, Department of Physiology, Antalya, Turkey.
Biol Trace Elem Res. 1996 Mar;51(3):249-57. doi: 10.1007/BF02784079.
Since the exact mechanism of manganese (Mn)-induced learning disability is not known, we investigated the role of elevated cholesterol in rats exposed daily to 357 and 714 micrograms Mn/kg for 39 d. Significant Mn accumulation was accompanied by increased cholesterol content in the hippocampal region of Mn-treated rats. The learning, which is based on the time needed to reach food placed at the exit of a T-maze after a 1-d training period, was significantly slower in exposed rats than in unexposed rats. The rats receiving 357 and 714 micrograms Mn/kg reached the food in 104.5 +/- 13.8 and 113.3 +/- 25.7 s, respectively, on d 30, whereas their untreated counterparts reached the food in 28.7 +/- 11.4 s. This delay was completely corrected to 29.3 +/- 7.8 and 30.7 +/- 6.0 s in rats with coadministration of an inhibitor of cholesterol biosynthesis with 357 and 714 micrograms/kg of Mn. The correction of impaired learning was associated with the normalization of hippocampal cholesterol, but the Mn level in this region of the brain was not influenced in rats treated with a drug that inhibits cholesterol biosynthesis. These results suggested that Mn-induced hypercholesterolemia is involved in Mn-dependent learning disability.
由于锰(Mn)诱发学习障碍的确切机制尚不清楚,我们研究了每日暴露于357和714微克锰/千克环境中39天的大鼠体内胆固醇升高的作用。锰处理组大鼠海马区锰显著蓄积,同时胆固醇含量增加。在经过1天训练期后,以到达T迷宫出口处食物所需时间为依据的学习能力,暴露组大鼠明显慢于未暴露组大鼠。在第30天,接受357和714微克锰/千克的大鼠分别在104.5±13.8秒和113.3±25.7秒到达食物,而未处理的对照组大鼠在28.7±11.4秒到达食物。在同时给予胆固醇生物合成抑制剂和357及714微克/千克锰的大鼠中,这种延迟完全纠正至29.3±7.8秒和30.7±6.0秒。学习障碍的纠正与海马胆固醇正常化相关,但在使用抑制胆固醇生物合成药物治疗的大鼠中,大脑该区域的锰水平未受影响。这些结果表明,锰诱导的高胆固醇血症与锰依赖性学习障碍有关。