Emel'ianova T G, Guzevatykh L S, Goriacheva N N, Andreeva L A, Alfeeva L Iu, Miasoedov N F
Izv Akad Nauk Ser Biol. 2005 Jan-Feb(1):47-54.
We studied the effect of a fragment of natural dermorphin (DM) precursor Arg-DM and its analogs (Pro-DM, 4Amino-Pro-DM, Mike et-DM, Kre-DM, Arg-[DArg2]-DM, and Arg-[DAla4]-DM after intraperitoneal administration on the functional status of the thermoregulation system in rats. The obtained data demonstrated that the hypothermic and vasomotor effects of Arg-DM were temperature-dependent and had the same pattern as DM (Emel'yanova et al., 1996). In the thermoneutral and room environment, the peptide induced a two-phase vascular response. The first phase was vasodilation; it was twice as strong as for DM and was not removed by naloxone pretreatment. The second phase was vasoconstriction; it was blocked by naloxone. Replacement of Arg with 4Amino-Pro, Met, and Kre as well as DAla2 to DArg2 or Gly4 to DAla4 replacements in the Arg-DM molecule affected the thermoregulatory activity of the peptide. For instance, only the vasodilation response was observed for Arg-[DAla2]-DM and Arg-[DAla4]-DM while only the vasoconstriction response was observed for 4Amino-Pro-DM.
我们研究了天然皮啡肽(DM)前体片段精氨酸 - DM及其类似物(脯氨酸 - DM、4 - 氨基 - 脯氨酸 - DM、甲硫氨酸 - DM、赖氨酸 - DM、精氨酸 - [D - 精氨酸2] - DM和精氨酸 - [D - 丙氨酸4] - DM)腹腔注射后对大鼠体温调节系统功能状态的影响。所得数据表明,精氨酸 - DM的降温及血管舒缩作用与温度有关,且与皮啡肽(Emel'yanova等人,1996年)具有相同模式。在热中性和室温环境中,该肽诱导出双相血管反应。第一阶段是血管舒张;其强度是皮啡肽的两倍,且纳洛酮预处理不能消除这种作用。第二阶段是血管收缩;它被纳洛酮阻断。在精氨酸 - DM分子中,用4 - 氨基 - 脯氨酸、甲硫氨酸和赖氨酸取代精氨酸,以及将丙氨酸2替换为D - 精氨酸2或甘氨酸4替换为D - 丙氨酸4,都会影响该肽的体温调节活性。例如,精氨酸 - [D - 丙氨酸2] - DM和精氨酸 - [D - 丙氨酸4] - DM仅观察到血管舒张反应,而4 - 氨基 - 脯氨酸 - DM仅观察到血管收缩反应。