Nanjo K, Kondo M, Sanke T, Nishi M
First Department of Medicine, Wakayama University of Medical Science, Japan.
Diabetes Res Clin Pract. 1994 Oct;24 Suppl:S135-41. doi: 10.1016/0168-8227(94)90240-2.
The recent development of molecular biology enables us to identify three abnormal insulins (insulin Chicago, insulin Los Angeles and insulin Wakayama). In Japan, three pedigrees in which affected individuals secrete [LeuA3] insulin (insulin Wakayama) have been identified. In each family, hyperinsulinemia associated with an abnormally elevated insulin to C-peptide molar ratio was demonstrated to occur in an autosomal dominant pattern of inheritance. In accordance with in vivo observations, semisynthetic [LeuA3] insulin demonstrated reduced in vitro receptor binding and biological activity relative to the human standard. The development of diabetes mellitus in affected family members was not uniform, was influenced by aging, and was different among families. Patients with impaired glucose tolerance demonstrated reduced insulin secretory reserve. Some of these features are thought to resemble the nature of non-insulin dependent diabetes mellitus (NIDDM). Therefore, insulin Wakayama may be a useful model for the study of the development of NIDDM.
分子生物学的最新进展使我们能够鉴定出三种异常胰岛素(芝加哥胰岛素、洛杉矶胰岛素和和歌山胰岛素)。在日本,已鉴定出三个家系,其中受影响的个体分泌[亮氨酸A3]胰岛素(和歌山胰岛素)。在每个家族中,与胰岛素与C肽摩尔比异常升高相关的高胰岛素血症被证明以常染色体显性遗传模式发生。与体内观察结果一致,半合成的[亮氨酸A3]胰岛素相对于人类标准品在体外显示出降低的受体结合和生物活性。受影响家庭成员中糖尿病的发展并不一致,受年龄影响,且在不同家族中有所不同。糖耐量受损的患者胰岛素分泌储备降低。这些特征中的一些被认为类似于非胰岛素依赖型糖尿病(NIDDM)的本质。因此,和歌山胰岛素可能是研究NIDDM发病机制的有用模型。