Tsukuda Kana, Mogi Masaki, Li Jian-Mei, Iwanami Jun, Min Li-Juan, Sakata Akiko, Fujita Teppei, Iwai Masaru, Horiuchi Masatsugu
Department of Molecular Cardiovascular Biology and Pharmacology, Ehime University, Graduate School of Medicine, Shitsukawa, Tohon, Ehime 791-0295, Japan.
Hypertension. 2007 Dec;50(6):1099-105. doi: 10.1161/HYPERTENSIONAHA.107.099374. Epub 2007 Oct 29.
Angiotensin II type-1 receptor blockers are widely used with the expectation of prevention of stroke, potential effects to ameliorate of type-2 diabetes, which seems to be closely associated with the impairment of cognitive function in humans. Recently, we have reported that an angiotensin II type-1 receptor blocker prevented cognitive impairment in mice after focal cerebral ischemia, at least partly through an angiotensin II type-2 receptor-mediated increase in a neuroprotective factor, methyl methanesulfonate sensitive-2. Here, we examined the possibility that an angiotensin II type-1 receptor blocker could improve cognitive function in a type-2 diabetic mouse model, KK-A(y). KK-A(y) mice subjected to 20 trials of a passive avoidance task every week from 8 weeks exhibited a significantly impaired avoidance rate, and moreover, its age-dependent decline, especially after 14 weeks of age, compared with age-matched C57BL6 mice. Oral administration of candesartan at a nonhypotensive dose (0.005% in laboratory chow) in KK-A(y) mice improved cognitive function and inhibited the impairment of cognitive decline. Methyl methanesulfonate sensitive-2 expression in the brain was lower in KK-A(y) mice than in C57BL6 mice. Treatment with candesartan markedly increased mRNA expression of angiotensin II type-2 receptor and methyl methanesulfonate sensitive-2 in the brain in KK-A(y) mice, determined by quantitative RT-PCR. In KK-A(y) mice treated with candesartan, age-dependent increases in blood glucose and insulin were significantly suppressed. Our results suggest that candesartan ameliorates the impaired cognitive function in type-2 diabetes mice, at least because of an increased expression of methyl methanesulfonate sensitive-2, a neuroprotective factor, in addition to improvement of glucose intolerance.
血管紧张素II 1型受体阻滞剂被广泛使用,期望能预防中风,对改善2型糖尿病可能有潜在作用,而2型糖尿病似乎与人类认知功能损害密切相关。最近,我们报道血管紧张素II 1型受体阻滞剂可预防局灶性脑缺血后小鼠的认知障碍,至少部分是通过血管紧张素II 2型受体介导的神经保护因子甲磺酸甲酯敏感-2的增加来实现的。在此,我们研究了血管紧张素II 1型受体阻滞剂能否改善2型糖尿病小鼠模型KK-A(y)的认知功能。从8周龄开始,每周对KK-A(y)小鼠进行20次被动回避任务试验,与年龄匹配的C57BL6小鼠相比,其回避率显著受损,而且其随年龄的下降,尤其是在14周龄后更为明显。以非降压剂量(在实验室饲料中为0.005%)口服坎地沙坦可改善KK-A(y)小鼠的认知功能,并抑制认知能力下降的损害。KK-A(y)小鼠大脑中甲磺酸甲酯敏感-2的表达低于C57BL6小鼠。通过定量RT-PCR测定,坎地沙坦治疗显著增加了KK-A(y)小鼠大脑中血管紧张素II 2型受体和甲磺酸甲酯敏感-2的mRNA表达。在用坎地沙坦治疗的KK-A(y)小鼠中,血糖和胰岛素随年龄的增加得到显著抑制。我们的结果表明,坎地沙坦可改善2型糖尿病小鼠受损的认知功能,至少部分原因是除了改善葡萄糖耐量异常外,神经保护因子甲磺酸甲酯敏感-2的表达增加。