Yao Jing, Shen Xin-nan, Shen Hui, Wu Min
Department of Nutrition and Food Hygiene, School of Public Health, Fudan University, Key Laboratory of Public Health Safety, Ministry of Education, Shanghai 200032, China.
Zhonghua Yu Fang Yi Xue Za Zhi. 2012 Jul;46(7):635-9.
To study the effects of theanine on dopamine (DA), 5-hydroxy tryptamine (5-TH) and glutamate receptor 2 (GluR2) mRNA, phospholipase-γ1 (PLC-γ1) mRNA in cerebral ischemia-reperfusion injury rats and explore the mechanism of protective effects of theanine on the induced brain injury by ischemia-reperfusion in rats.
According to random number table, a total of 56 sprague-dawley rats in SPF grade about six-week old and 100 - 120 grams weighting were divided into five groups according to the body weight levels: model group (n = 12), sham-operation group (n = 8), low theanine group (10 mg/kg), middle theanine group (30 mg/kg) and high theanine group (90 mg/kg). There were 12 rats in each of the theanine group. The rats in model group and sham-operation groups were given distilled water, and the rats in theanine groups were given corresponding theanine solution intragastrically for fifteen days. Then the cerebral ischemia-reperfusion injury was established by middle cerebral artery occlusion (MCAO). The score of neurological behavior was evaluated at the 3rd and 24th hours after reperfusion. Rats were sacrificed at 24 hours after reperfusion, the concentrations of DA, 5-HT and theanine in rats brain following ischemia-reperfusion were determined. At the same time, we determined the levels of reactive oxygen species (ROS) and activities of catalase (CAT) in mitochondria of brain. The expressions of GluR2 mRNA and PLC-γ1 mRNA in rat brain were examined by reverse transcription polymerase chain reaction (RT-PCR) technique.
The score of neurological behavior of rats in model group, theanine-low, middle, high dose groups at the 3rd hour was 6.000 ± 0.926, 4.100 ± 0.738, 3.444 ± 0.726 and 2.250 ± 0.886 respectively (F = 29.70, P < 0.01), and the score at the 24th hour in these groups was 6.625 ± 0.916, 5.000 ± 0.817, 3.667 ± 0.707 and 2.625 ± 0.916 respectively(F = 34.68, P < 0.01). The concentration of DA in model group, theanine-low, middle, high dose groups and sham-operation group was (10.26 ± 1.12), (12.48 ± 1.09), (14.55 ± 0.94), (15.97 ± 0.92) and (11.98 ± 0.63) µg/g respectively (F = 43.76, P < 0.01). The concentration of 5-HT in these groups was (1.091 ± 0.160), (0.818 ± 0.101), (0.571 ± 0.050), (0.453 ± 0.111) and (0.863 ± 0.063) µg/g respectively (F = 48.68, P < 0.01). The level of ROS was (3.072 ± 0.503), (1.331 ± 0.268), (1.295 ± 0.061), (0.804 ± 0.200) and (2.158 ± 0.218) U×min⁻¹×mg⁻¹ (F = 80.82, P < 0.01) respectively and the activities of CAT in these groups were (4.880 ± 1.121), (8.405 ± 1.356), (9.535 ± 2.511), (15.090 ± 4.054) and (21.260 ± 6.054) U/g respectively (F = 28.58, P < 0.01). The expressions of GluR2 mRNA were 0.842 ± 0.020, 1.063 ± 0.100, 1.170 ± 0.152, 1.254 ± 0.131 and 1.012 ± 0.056 respectively (F = 9.23, P < 0.01). The expressions of PLC-γ1 mRNA in these groups were 0.737 ± 0.090, 0.887 ± 0.045, 0.963 ± 0.025, 0.991 ± 0.049 and 0.867 ± 0.079 respectively(F = 10.24, P < 0.01).
Theanine has a protective effect on the induced brain injury by ischemia-reperfusion in rats, which might be associated with its interaction with monoamine neurotransmitters and up-regulating the expressions of GluR2 mRNA and PLC-γ1 mRNA.
研究茶氨酸对脑缺血再灌注损伤大鼠多巴胺(DA)、5-羟色胺(5-TH)、谷氨酸受体2(GluR2)mRNA、磷脂酶-γ1(PLC-γ1)mRNA的影响,探讨茶氨酸对大鼠缺血再灌注诱导脑损伤的保护作用机制。
按照随机数字表,将56只6周龄左右、体重100 - 120克的SPF级Sprague-Dawley大鼠按体重水平分为5组:模型组(n = 12)、假手术组(n = 8)、低剂量茶氨酸组(10毫克/千克)、中剂量茶氨酸组(30毫克/千克)和高剂量茶氨酸组(90毫克/千克)。茶氨酸组每组12只大鼠。模型组和假手术组大鼠给予蒸馏水,茶氨酸组大鼠给予相应茶氨酸溶液灌胃15天。然后通过大脑中动脉闭塞(MCAO)建立脑缺血再灌注损伤模型。在再灌注后3小时和24小时评估神经行为评分。再灌注24小时后处死大鼠,测定缺血再灌注后大鼠脑内DA、5-HT和茶氨酸的浓度。同时,测定脑线粒体中活性氧(ROS)水平和过氧化氢酶(CAT)活性。采用逆转录聚合酶链反应(RT-PCR)技术检测大鼠脑内GluR2 mRNA和PLC-γ1 mRNA的表达。
模型组、低剂量茶氨酸组、中剂量茶氨酸组、高剂量茶氨酸组大鼠在3小时时的神经行为评分为6.000 ± 0.926、4.100 ± 0.738、3.444 ± 0.726和2.250 ± 0.886,F = 29.70,P < 0.01;在24小时时这些组的评分为6.625 ± 0.916、5.000 ± 0.817、3.667 ± 0.707和2.625 ± 0.916,F = 34.68,P < 0.01。模型组、低剂量茶氨酸组、中剂量茶氨酸组、高剂量茶氨酸组和假手术组大鼠脑内DA浓度分别为(10.26 ± 1.12)、(12.48 ± 1.09)、(14.55 ± 0.94)、(15.97 ± 0.92)和(11.98 ± 0.63)微克/克,F = 43.76,P < 0.01。这些组的5-HT浓度分别为(1.091 ± 0.160)、(0.818 ± 0.101)、(0.571 ± 0.050)、(0.453 ± 0.111)和(0.863 ± 0.063)微克/克,F = 48.68,P < 0.01。ROS水平分别为(3.072 ± 0.503)、(1.331 ± 0.268)、(1.295 ± 0.061)、(0.804 ± 0.200)和(2.158 ± 0.218)U×min⁻¹×mg⁻¹,F = 80.82,P < 0.01;这些组的CAT活性分别为(4.880 ± 1.121)、(8.405 ± 1.356)、(9.535 ± 2.511)、(15.090 ± 4.054)和(21.260 ± 6.054)U/克,F = 28.58,P < 0.01。GluR2 mRNA的表达分别为0.842 ± 0.020、1.063 ± 0.100、1.170 ± 0.152、1.254 ± 0.131和1.012 ± 0.056,F = 9.23,P < 0.01。这些组PLC-γ1 mRNA的表达分别为0.737 ± 0.090、0.887 ± 0.045、0.963 ± 0.025、0.991 ± 0.049和0.867 ± 0.079,F = 10.24,P < 0.01。
茶氨酸对大鼠缺血再灌注诱导的脑损伤具有保护作用,这可能与其与单胺类神经递质相互作用以及上调GluR2 mRNA和PLC-γ1 mRNA的表达有关。