论文部分内容阅读
以Fura2/AM为细胞内钙离子的荧光指示剂,用ARCMMIC阳离子测定系统,直接测定了体外培养的新生大鼠神经细胞内游离钙([Ca2+]i)值,并观察了小檗碱(Ber)的影响。结果表明,Ber对神经细胞静息[Ca2+]i无明显影响,Ber1~100μmol·L-1能剂量依赖地抑制去甲肾上腺素和H2O2引起的[Ca2+]i升高,其IC50分别为39.9和17.9μmol·L-1。高剂量Ber(10~100μmol·L-1)能抑制高K+引起的[Ca2+]i升高。姐果提示,Ber对去甲肾上腺素,高K+及H2O2引起的[Ca2+]i升高的抑制作用可能是其抗脑缺血作用机制之一。
Fura 2 / AM as a fluorescent indicator of intracellular calcium with ARCMICM cation determination system, directly measured in vitro cultured neonatal rat intracellular free calcium ([Ca2] i) value and observed The effect of berberine (Ber). The results showed that Ber had no effect on resting [Ca2 +] i in neurons. Ber1 ~ 100μmol·L-1 dose-dependently inhibited the increase of [Ca2 +] i induced by norepinephrine and H2O2 with IC50 of 39. 9 and 17.9μmol·L-1. High doses of Ber (10 ~ 100μmol·L-1) inhibited the increase of [Ca2 +] i induced by high K +. Sister fruit suggest that Ber on norepinephrine, high K + and H2O2-induced [Ca2 +] i inhibition may be one of its anti-cerebral ischemia mechanism.