Gill-Randall R J, Adams D, Ollerton R L, Alcolado J C
Department of Medicine, University of Wales College of Medicine, Heath Park, Cardiff CF14 4XN, Wales, UK.
Diabet Med. 2004 Jul;21(7):759-62. doi: 10.1111/j.1464-5491.2004.01225.x.
Patients with Type 2 diabetes mellitus more often report a history of an affected mother than father. However, in the few studies where both parents and offspring have been directly tested, this apparent maternal excess has not been confirmed. Rodent models of diabetes have the advantage that all parents and offspring can undergo glucose tolerance testing at a specific age in adult life. The aim of this study was to gain insights into the inheritance of human Type 2 diabetes by using a rat model.
Goto Kakizaki (GK) rats (a model of Type 2 diabetes) were mated with non-diabetic Wistar rats. Offspring were produced from 20 GK female vs. Wistar male and 20 Wistar female vs. GK male crosses. Fasting blood glucose was measured at 6 weeks and 3 months of age and an intravenous glucose tolerance test (0.8 g/kg) performed at 6 months of age.
Wistar mothers produced litters with almost twice as many viable offspring as GK mothers (14.1 vs. 7.4, P < 0.001). Despite the larger litter size, offspring in the two groups were of comparable weight at 6 weeks and 6 months of age. At 3 months of age, male offspring of Wistar mothers were heavier than offspring of GK mothers (415.7 g vs. 379.5 g, P = 0.016) but this difference was not sustained at 6 months of age. Fasting blood glucose at all ages and average blood glucose during the glucose tolerance test were similar in both groups.
We therefore conclude that there is no evidence for maternal transmission of diabetes in the GK rat. Mothers were able to adjust their supply of milk so that offspring attained similar weights independent of litter size. The weight of the offspring remained independent of litter size into adult life.
2型糖尿病患者更常报告其母亲而非父亲有患病史。然而,在少数对父母及其后代都进行了直接检测的研究中,这种明显的母系遗传优势并未得到证实。糖尿病啮齿动物模型的优势在于,所有的亲代和子代都能在成年后的特定年龄接受葡萄糖耐量测试。本研究的目的是通过使用大鼠模型来深入了解人类2型糖尿病的遗传方式。
将Goto Kakizaki(GK)大鼠(一种2型糖尿病模型)与非糖尿病的Wistar大鼠进行交配。通过20组GK雌性大鼠与Wistar雄性大鼠以及20组Wistar雌性大鼠与GK雄性大鼠的杂交产生后代。在6周龄和3月龄时测量空腹血糖,并在6月龄时进行静脉葡萄糖耐量试验(0.8 g/kg)。
Wistar母鼠产仔的存活后代数量几乎是GK母鼠的两倍(14.1只对7.4只,P < 0.001)。尽管窝仔数较多,但两组后代在6周龄和6月龄时体重相当。在3月龄时,Wistar母鼠的雄性后代比GK母鼠的后代更重(415.7 g对379.5 g,P = 0.016),但这种差异在6月龄时并未持续存在。两组在所有年龄段的空腹血糖以及葡萄糖耐量试验期间的平均血糖均相似。
因此,我们得出结论,在GK大鼠中没有证据表明糖尿病存在母系遗传。母鼠能够调整其乳汁供应,以使后代无论窝仔数多少都能达到相似的体重。后代的体重在成年后仍与窝仔数无关。