Zhong Zhen-Dong, Wang Chun-Mei, Wang Wei, Shen Li, Chen Zhong-Hua
Sichuan Da Xue Xue Bao Yi Xue Ban. 2014 Mar;45(2):235-9.
To explore the mechanism of Panax notoginseng saponins (PNS) on diabetes treatment and mass loss in KK-Ay mice with genetic type 2 diabetes mellitus (DM), and to identify the main hypoglycemic ingredients.
C57 and KK-Ay DM mice were divided into eight groups each comprising six mice: healthy normal, DM model, and DM model treated with PNS (200 mg/kg body mass), ginsenoside Re (Re, 14 mg/kg body mass), ginsenoside Rd (Rd, 15 mg/kg body mass), ginsenoside Rgl (Rg1, 40 mg/kg body mass), ginsenoside Rb1 (Rb1, 60 mg/kg body mass) and notoginsenoside R1 (R1, 6 mg/kg body mass). The PNS were intraperitoneal injection administered for 30 d, while the Re, RB1, Rg1, Rd and Re were intraperitoneal injection administered for 12 d. The fasting blood sugar (FBG), glucose tolerance (GT), serum insulin, leptin, body weight, food consumption, and levels of adipose tissue and blood lipid were determined.
On 12 d, lower FBG levels were found in the PNS and Rb1 treated mice compared with the model mice (P < 0.05). No statistical differences in FBG levels were found between the rest of the treatment groups and the model group (P > 0.05). After 30 d continuous administration of PNS, the FBG level of the mice further declined (P < 0.01). Meanwhile, the serum insulin (P < 0.05) and insulin resistance index (P < 0.01) of the PNS treated mice also declined significantly. Compared with model group, the PNS group had lower levels of body weight growth, food consumption, adipose tissue, and leptin (P < 0.05). Lower FBG level was also found in Rb1 treated mice (12 d of administration), P < 0.05.
PNS has anti-hyperglycemic and anti-obesity activities by improving insulin and leptin sensitivities in KK-Ay mice. Rb1 may be the hypoglycemic ingredient in the PNS extract.
探讨三七总皂苷(PNS)对2型遗传性糖尿病(DM)KK-Ay小鼠糖尿病治疗及体重减轻的作用机制,并确定主要的降血糖成分。
将C57和KK-Ay DM小鼠各分为8组,每组6只:健康正常组、DM模型组以及用PNS(200mg/kg体重)、人参皂苷Re(Re,14mg/kg体重)、人参皂苷Rd(Rd,15mg/kg体重)、人参皂苷Rg1(Rg1,40mg/kg体重)、人参皂苷Rb1(Rb1,60mg/kg体重)和三七皂苷R1(R1,6mg/kg体重)治疗的DM模型组。PNS腹腔注射给药30天,而Re、RB1、Rg1、Rd和Re腹腔注射给药12天。测定空腹血糖(FBG)、糖耐量(GT)、血清胰岛素、瘦素、体重、食物摄入量以及脂肪组织和血脂水平。
在第12天,与模型小鼠相比,PNS和Rb1治疗的小鼠FBG水平较低(P<0.05)。其余治疗组与模型组之间的FBG水平无统计学差异(P>0.05)。连续30天给予PNS后,小鼠的FBG水平进一步下降(P<0.01)。同时,PNS治疗小鼠的血清胰岛素(P<0.05)和胰岛素抵抗指数(P<0.01)也显著下降。与模型组相比,PNS组的体重增长、食物摄入量、脂肪组织和瘦素水平较低(P<0.05)。Rb1治疗的小鼠(给药12天)FBG水平也较低,P<0.05。
PNS通过改善KK-Ay小鼠的胰岛素和瘦素敏感性而具有降血糖和抗肥胖活性。Rb1可能是PNS提取物中的降血糖成分。