Mitrović Milena, Pantelinac Pavle, Radosavljević Jovanka, Bajkin Ivana, Todorović-Dilas Ljiljana
Medicinski fakultet Novi Sad.
Med Pregl. 2006 Nov-Dec;59(11-12):539-44. doi: 10.2298/mpns0612539m.
Ever since insulin was discovered by Banting and Best in 1921, all further researches in this field had been conducted with one goal: to find new insulin molecules which would provide better glycemic control with fewer side effects i.e. to mimic endogenous physiological insulin secretion.
In healthy individuals, endogenous insulin secretion can be classified as basal (which provides basal glucose homeostasis) and stimulated (as a response to a meal). Conventional insulin preparations--human insulin, have time-action profiles that cannot fully immitate endogenous insulin secretion, thus leading to postprandial hyperglicemia and high glycemic oscilations during the day. RAPID-ACTING ANALOGUES: Rapid acting analogues should have a time-action profile with onset of less than one hour, duration less than four hours, hypoglycemic potency equal or greater than that of human insulin, and similar effects in all patients. Two rapid action analogues, lispro and aspart are available.
The ideal basal insulin should provide slow and constant absorption, long half-life that would provide once daily dosing (or every other day), and peakless effect. Insulin glargine led to solubility at pH 4 and to slow absorption in neutral pH environment. Insulin detemir is a soluble insulin analogue with neutral pH and affinity to bind to serum albumin, thus gaining prolonged action.
The mitogenic influence of insulin is due to the affinity to bind to IGF-I receptors. Following two-year administration of glargine in mice and rats, systemic carcinogenic potential was not found, though there were reports of hepatocellular carcinomas, which are frequently found in these animals.
In the last two decades, many trials have shown that unsatisfactory glycemic control leads to chronic complications in both types of diabetes. Using basal glucose level, postprandial glycemy and HbA1c as metabolic parameters, it has been proven that only strict glycemic control can lower the risk of developing complications. Discovery of insulin analogues (both rapid acting and basal) enables physicians to provide better glycoregulation and less hypoglycemic incidents to their patients.
自1921年班廷和贝斯特发现胰岛素以来,该领域的所有进一步研究都朝着一个目标进行:寻找新的胰岛素分子,以期在副作用更少的情况下实现更好的血糖控制,即模拟内源性生理性胰岛素分泌。
在健康个体中,内源性胰岛素分泌可分为基础分泌(维持基础血糖稳态)和刺激后分泌(对进食的反应)。传统胰岛素制剂——人胰岛素,其作用时间曲线无法完全模拟内源性胰岛素分泌,从而导致餐后高血糖和日间血糖大幅波动。
速效类似物的作用时间曲线应具备起效时间少于1小时、持续时间少于4小时、降血糖效力等于或大于人胰岛素,且对所有患者效果相似的特点。目前有两种速效类似物,即赖脯胰岛素和门冬胰岛素。
理想的基础胰岛素应具有缓慢且持续的吸收、长半衰期以实现每日一次给药(或隔日一次)以及无峰值效应。甘精胰岛素在pH 4时可溶解,并在中性pH环境中缓慢吸收。地特胰岛素是一种pH呈中性且能与血清白蛋白结合的可溶性胰岛素类似物,因此作用时间延长。
胰岛素的促有丝分裂作用归因于其与胰岛素样生长因子-I受体结合的亲和力。在小鼠和大鼠中给予甘精胰岛素两年后,未发现全身致癌潜力,尽管有肝细胞癌的报道,而肝细胞癌在这些动物中较为常见。
在过去二十年中,许多试验表明,血糖控制不佳会导致两种类型糖尿病的慢性并发症。以基础血糖水平、餐后血糖和糖化血红蛋白作为代谢参数,已证实只有严格的血糖控制才能降低并发症发生风险。胰岛素类似物(速效和基础胰岛素)的发现使医生能够为患者提供更好的血糖调节并减少低血糖事件。