Effects of Haematococcus pluvialis astaxanthin on diabetes mice for decreasing blood glucose and its mechanisms
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摘要: 通过尾静脉注射四氧嘧啶(4550 mg/kg BW iv)建立小鼠高血糖模型,研究雨生红球藻源虾青素(astaxanthin,ASX)对四氧嘧啶高血糖小鼠血糖的调节作用。分别以雨生红球藻源虾青素粉(虾青素含量为2%)25、100 mg/kg连续灌胃高血糖小鼠14 d,在末次灌胃后摘眼球取血测定血糖、胰岛素、SOD、GSH-Px的活性和MDA水平;肝、肾组织称重并测定SOD、GSH-Px的活性和MDA水平。结果表明,雨生红球藻源虾青素可缓解高血糖模型小鼠体重降低的趋势,减少饮水量和摄食量;雨生红球藻源虾青素可显著降低四氧嘧啶高血糖小鼠的血糖值(p<0.05)以及极显著提高血清中胰岛素的含量(p<0.01),增强血清中的SOD(p<0.05)和GSH-Px(p<0.01)的活性,抑制了肾脏和肝脏中的MDA水平。结果表明,提高血清和肝肾组织的抗氧化能力,增加机体内的胰岛素水平可能是雨生红球藻源虾青素降血糖的机制之一。Abstract: To explore effect of Haematococcus pluvialis astaxanthin to mice diabete for decreasing blood glucose and its mechanisms. Experimental diabete mice was induced by alloxan( ALX)( 45 ~ 50 mg / kg BW iv). With25 mg / kg and 100 mg / kg dose of Haematococcus pluvialis astaxanthin( 2%) for 14 d lavage alloxan diabete mice,the blood samples of mice were collected by orbit,blood glucose,insulin,SOD,GSH- Px activity and MDA level in the blood were measured.The liver and kidney were taken to weigh,SOD,GSH- Px activity and MDA level in the tissues were measured.The results showed that Haematococcus pluvialis astaxanthin could significantly( p < 0.05)inhibit diabete mice weight of reduction and return to normal,reduce( p < 0.01) water intake and diet intake and reduce( p < 0.01) high blood glucose levels of diabete mice and improve the ability of antioxidation,the mechanism of ASX in reducing blood glucose might be achieved by regulating the insulin.
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Keywords:
- Haematococcus pluvialis /
- astaxanthin /
- blood glucos /
- diabetes /
- mice
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[1] Shi CH,Wang C,Bai R,et al.Associations among glycemic excursions,glycated hemoglobin andhigh-sensitivity Creactiveprotein in patients with poorly controlled type 2 diabetes mellitus[J].Experimental and Therapeutic Medicine,2015,10(5):1937-1942.
[2] Bjornstad P,Cherney D,Maahs DM.Early diabetic nephropathy in type 1 diabetes:new insights[J].Curr Opin Endocrinol Diabetes Obes,2014,4(21):279-286.
[3] Boukhris M,Tomasello SD,Marza F,et al.Coronary Heart Disease in Postmenopausal women with Type II Diabetes Mellitus and the Impact of Estrogen Replacement Therapy:A Narrative Review[J].Int J Endocrinol,2014:413920.
[4] Richard P,Shin P,Beeson T,et al.Quality and Cost of Diabetes Mellitus Care in Community Health Centers in the United States[J].PLo S One,2015,12(10):e0144075.
[5] Marciniak C,Marechal X,Montaigne D,et al.Cardiac contractile function and mitochondrial respiration in diabetesrelated mouse models[J].Cardiovasc Diabetol,2014(13):118.
[6] Zimmet P,Alberti KG,Shaw J.Global and societal implications of the diabetes epidemic[J].Nature,2001,414:782-787.
[7] Ambati RR,Phang SM,Ravi S,et al.Astaxanthin:sources,extraction,stability,biological activities and its commercial applications--a review[J].Mar Drugs,2014,12(1):128-152.
[8] Saw CL,Yang AY,Guo Y,et al.Astaxanthin and omega-3fatty acids individually ang in combination protect against oxidative stress via the Nrf2-ARE pathway[J].Food and Chemical Toxicology,2013,62:869-875.
[9] Polotow TG,Vardaris CV,Mihaliuc AR,et al.Astaxanthin supplementation delays physical exhaustion and prevents redox imbalances in plasma and soleus muscles of Wistar rats[J].Nutrients,2014,12(6):5819-5838.
[10] Ursoniu S,Sahebkar A,Serban MC,et al.Lipid profile and glucose changes after supplementation with astaxanthin:a systematic review and meta-analysis of randomized controlled trials[J].Arch Med Sci,2015,11(2):253-266.
[11] Ciccone MM,Cortese F,Gesualdo M,et al.Dietary intake of carotenoids and their antioxidant andanti-inflammatory effects in cardiovascular care[J].Mediators Inflamm,2013:782137.
[12] Bhuvaneswari S,Yogalakshmi B,Sreeja S,et al.Astaxanthin reduces hepatic endoplasmic reticulum stress and nuclear factorkappa B-mediated inflammation in high fructose and high fat diet-fed mice[J].Cell Stress Chaperones,2014,19(2):183-191.
[13] Xu J,Gao H,Zhang L,et al.A combination of flaxseed oil and astaxanthin alleviates atherosclerosis risk factors in high fat diet fed rats[J].Lipids Health Dis,2014,13:63.
[14] Yadav P,Sarker S,Bhatnager D.Action of Capparis decidua against alloxan inducedoxidative stress and diabetes in rat tissues[J].Pharmacol Res,1997,36(3):221-228.
[15] Chakarabarti R,Vikramadithyan RK,Mullangi R,et al.Antidiabetic and hypolipidemic activity of Helicteres isora in animal models[J].J Ethnopharmacol,2002,81:343-349.
[16] Feillet-Coudary C,Rock E,Coudyar C,et al.Lipid peroxidation and antioxidant status in experimental diabetes[J].Clin Clim Aeta,1999,284:31-43.
[17] Lesley K,Mac Donald Wicks,Manohar L G.Vitamin E supplementation in the mitigation ofcarbontetrachloride induced oxidative stress in rats[J].J Nutr Biochem,2003,14:211-218.
[18] Laybutt R,Hasenkma PW,Groff A,et al.B-cell adaptation to hypegrlyeemia[J].Diabetes,2001,50:s180-s181.
[19] Choi HD,Youn YK,Shin W.Positive effects of astaxanthin on lipid profiles and oxidative stress in overweight subjects[J].Plant Food for Human Nutrition,2011,66(4):363-369.
[20] Samols E,Bonne-Welr S,Weir GC.Intra-islet insulinglucagon-somatostatinrelationships[J].Clin Endocrind Metab,2013,15(1):33-58.
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