Serino R, Ueta Y, Tokunaga M, Hara Y, Nomura M, Kabashima N, Shibuya I, Hattori Y, Yamashita H
Department of Physiology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Diabetologia. 1998 Jun;41(6):640-8. doi: 10.1007/s001250050962.
Plasma arginine vasopressin (AVP) is known to be elevated in patients with uncontrolled insulin-dependent diabetes mellitus who have plasma hyperosmolality with hyperglycaemia. Although osmotic stimuli cause an increase in nitric oxide synthase (NOS) activity as well as synthesis of AVP and oxytocin in the paraventricular (PVN) and supraoptic nuclei (SON), it is not known whether NOS activity in the hypothalamus changes in the diabetic patients who have plasma hyperosmolality with hyperglycaemia caused by insulin deficiency. Expression of the neuronal (n) NOS gene in the PVN and SON in streptozotocin (STZ)-induced diabetic rats was investigated by using in situ hybridization histochemistry and NADPH-diaphorase histochemical staining. Four weeks after intraperitoneal (i. p.) administration of STZ, male Wistar rats developed hyperglycaemia and plasma hyperosmolality. The expression of nNOS gene and NADPH-diaphorase staining in the PVN and SON remarkably increased in STZ-induced diabetic rats compared to control rats. Three weeks after administration of STZ, the diabetic rats were subcutaneously treated with insulin for 1 week, which resulted in significant suppression of the induction of nNOS, AVP and oxytocin gene expression in the PVN and SON. Furthermore, the induction of nNOS gene expression in the PVN and SON was suppressed in STZ-induced diabetic rats treated with phlorizin and diet to normalize hyperglycaemia without insulin treatment. These results suggest that upregulation of nNOS gene expression as well as AVP and oxytocin gene expression in the PVN and SON in STZ-induced diabetic rats may be associated with hyperglycaemia and plamsa hyperosmolality.
已知在患有血浆高渗伴高血糖的胰岛素依赖型糖尿病未控制患者中,血浆精氨酸加压素(AVP)会升高。尽管渗透压刺激会导致室旁核(PVN)和视上核(SON)中一氧化氮合酶(NOS)活性增加以及AVP和催产素合成增加,但尚不清楚在因胰岛素缺乏导致血浆高渗伴高血糖的糖尿病患者中,下丘脑的NOS活性是否会发生变化。通过原位杂交组织化学和NADPH-黄递酶组织化学染色,研究了链脲佐菌素(STZ)诱导的糖尿病大鼠PVN和SON中神经元型(n)NOS基因的表达。腹腔注射STZ四周后,雄性Wistar大鼠出现高血糖和血浆高渗。与对照大鼠相比,STZ诱导的糖尿病大鼠PVN和SON中nNOS基因的表达及NADPH-黄递酶染色显著增加。给予STZ三周后,对糖尿病大鼠皮下注射胰岛素一周,这导致PVN和SON中nNOS、AVP和催产素基因表达的诱导受到显著抑制。此外,在用根皮苷和饮食治疗以在不进行胰岛素治疗的情况下使高血糖正常化的STZ诱导的糖尿病大鼠中,PVN和SON中nNOS基因表达的诱导也受到抑制。这些结果表明,STZ诱导的糖尿病大鼠PVN和SON中nNOS基因表达以及AVP和催产素基因表达的上调可能与高血糖和血浆高渗有关。