Kirchgessner M, Moser C, Roth H P
Institute of Nutrition Physiology, Technical University Munich, Freising-Weihenstephan, Germany.
Biol Trace Elem Res. 1996 Jun;52(3):273-80. doi: 10.1007/BF02789168.
The purpose of the present study was to investigate, in force-fed rats, whether alimentary zinc (Zn) deficiency affects the activity of the Zn-metalloenzyme protein kinase C (PKC). The in vivo activity of PKC was determined by measuring the subcellular distribution of the enzyme between the cytosolic and the particulate fraction in brain and muscle. For this purpose, 24 male Sprague-Dawley rats with an average live mass of 126 g were divided into 2 groups of 12 animals each. The Zn-deficient and the control rats received a semisynthetic casein diet with a Zn content of 1.2 and 24.1 ppm, respectively. All animals were fed four times daily by gastric tube in order to ensure that the depleted animals also received adequate nutrients and to synchronize the feed intake exactly. After 12 d, the depleted rats were in a state of severe Zn deficiency, as demonstrated by a 70% lower serum Zn concentration and a 66% reduction in the serum activity of alkaline phosphatase. Neither the cytosolic nor the particulate fraction of the thigh muscle showed any difference between the depleted and the control animals as regards PKC activity/g of muscle. The specific activity of PKC/mg of protein in the cytosolic fraction of the muscle was not affected by alimentary zinc deficiency, whereas the specific activity of PKC in the particulate fraction of the muscle was reduced by a significant 10% in Zn deficiency (150 +/- 12 vs 135 +/- 14 pmol P/min/mg protein). In the brain, neither the cytosolic nor the particulate fraction revealed any difference in PKC activity/g of fresh weight or in the specific activity/mg of protein between the control and the Zn-deficient rats.
本研究的目的是在强制喂食的大鼠中,探究膳食锌(Zn)缺乏是否会影响锌金属酶蛋白激酶C(PKC)的活性。通过测量大脑和肌肉中细胞溶质和颗粒部分之间该酶的亚细胞分布来确定PKC的体内活性。为此,将24只平均体重为126 g的雄性Sprague-Dawley大鼠分为两组,每组12只。缺锌组和对照组大鼠分别接受锌含量为1.2 ppm和24.1 ppm的半合成酪蛋白饮食。为确保缺锌动物也能获得足够的营养并精确同步采食量,所有动物每天通过胃管喂食四次。12天后,缺锌大鼠处于严重锌缺乏状态,血清锌浓度降低70%,血清碱性磷酸酶活性降低66%,即证明了这一点。就每克肌肉的PKC活性而言,缺锌组和对照组动物的大腿肌肉细胞溶质部分和颗粒部分均未显示出任何差异。膳食锌缺乏并未影响肌肉细胞溶质部分每毫克蛋白质的PKC比活性,而在锌缺乏状态下,肌肉颗粒部分的PKC比活性显著降低了10%(分别为150±12和135±14 pmol P/分钟/毫克蛋白质)。在大脑中,对照组和缺锌组大鼠之间,无论是每克鲜重的PKC活性还是每毫克蛋白质的比活性,细胞溶质部分和颗粒部分均未显示出任何差异。