Rizzo Manfredi, Abate Nicola, Chandalia Manisha, Rizvi Ali A, Giglio Rosaria V, Nikolic Dragana, Marino Gammazza Antonella, Barbagallo Ignazio, Isenovic Esma R, Banach Maciej, Montalto Giuseppe, Li Volti Giovanni
Biomedical Department of Internal Medicine and Medical Specialties (M.R., R.V.G., D.N., G.M.), University of Palermo, Palermo 90127, Italy; Euro-Mediterranean Institute of Science and Technology (M.R., A.M.G., I.B., G.L.V.), Palermo 90139, Italy; Division of Endocrinology, Diabetes and Metabolism (M.R., A.A.R.), University of South Carolina School of Medicine, Columbia, South Carolina 29203; Division of Endocrinology (N.A., M.C.), The University of Texas Medical Branch, Galveston, Texas 77555; Department of Experimental Biomedicine and Clinical Neurosciences (A.M.G.), University of Palermo, Palermo 90127, Italy; Department of Drug Sciences (I.B.), University of Catania, Catania 90125, Italy; Laboratory for Molecular Genetics and Radiobiology (E.R.I.), Vinca Institute, University of Belgrade, Belgrade 11000, Serbia; Department of Hypertension (M.B.), Medical University of Lodz, Lodz 90-549, Poland; and Department of Biomedical and Biotechnological Sciences (G.L.V.), University of Catania, Catania 90125, Italy.
J Clin Endocrinol Metab. 2015 Feb;100(2):603-6. doi: 10.1210/jc.2014-2291. Epub 2014 Nov 13.
Liraglutide is a glucagon-like peptide-1 analog and glucose-lowering agent whose effects on cardiovascular risk markers have not been fully elucidated.
We evaluated the effect of liraglutide on markers of oxidative stress, heme oxygenase-1 (HO-1), and plasma ghrelin levels in patients with type-2 diabetes mellitus (T2DM).
A prospective pilot study of 2 months' duration has been performed at the Unit of Diabetes and Cardiovascular Prevention at University of Palermo, Italy. Patients and Intervention(s): Twenty subjects with T2DM (10 men and 10 women; mean age: 57 ± 13 y) were treated with liraglutide sc (0.6 mg/d for 2 wk, followed by 1.2 mg/d) in addition to metformin (1500 mg/d orally) for 2 months. Patients with liver disorders or renal failure were excluded.
MAIN OUTCOME MEASURE(S): Plasma ghrelin concentrations, oxidative stress markers, and heat-shock proteins, including HO-1 were assessed.
The addition of liraglutide resulted in a significant decrease in glycated hemoglobin (HbA1c) (8.5 ± 0.4 vs 7.5 ± 0.4%, P < .0001). In addition, plasma ghrelin and glutathione concentrations increased (8.2 ± 4.1 vs 13.6 ± 7.3 pg/ml, P = .0007 and 0.36 ± 0.06 vs 0.44 ± 0.07 nmol/ml, P = .0002, respectively), whereas serum lipid hydroperoxides and HO-1 decreased (0.11 ± 0.05 vs 0.04 ± 0.07 pg/ml, P = .0487 and 7.7 ± 7.7 vs 3.6 ± 1.8 pg/ml, P = .0445, respectively). These changes were not correlated with changes in fasting glycemia or HbA1c.
In a 2-months prospective pilot study, the addition of liraglutide to metformin resulted in improvement in oxidative stress as well as plasma ghrelin and HO-1 concentrations in patients with T2DM. These findings seemed to be independent of the known effects of liraglutide on glucose metabolism.
利拉鲁肽是一种胰高血糖素样肽-1类似物和降糖药物,其对心血管风险标志物的影响尚未完全阐明。
我们评估了利拉鲁肽对2型糖尿病(T2DM)患者氧化应激标志物、血红素加氧酶-1(HO-1)和血浆胃饥饿素水平的影响。
在意大利巴勒莫大学糖尿病与心血管预防科进行了一项为期2个月的前瞻性初步研究。患者与干预措施:20例T2DM患者(10名男性和10名女性;平均年龄:57±13岁)除口服二甲双胍(1500mg/d)外,皮下注射利拉鲁肽(第1周0.6mg/d,之后1.2mg/d),持续2个月。排除患有肝脏疾病或肾衰竭的患者。
评估血浆胃饥饿素浓度、氧化应激标志物和热休克蛋白,包括HO-1。
加用利拉鲁肽后糖化血红蛋白(HbA1c)显著降低(8.5±0.4 vs 7.5±0.4%,P<.0001)。此外,血浆胃饥饿素和谷胱甘肽浓度升高(分别为8.2±4.1 vs 13.6±7.3 pg/ml,P=.0007和0.36±0.06 vs 0.44±0.07 nmol/ml,P=.0002),而血清脂质过氧化物和HO-1降低(分别为0.11±0.05 vs 0.04±0.07 pg/ml,P=.0487和7.7±7.7 vs 3.6±1.8 pg/ml,P=.0445)。这些变化与空腹血糖或HbA1c的变化无关。
在一项为期2个月的前瞻性初步研究中,T2DM患者在二甲双胍基础上加用利拉鲁肽可改善氧化应激以及血浆胃饥饿素和HO-1浓度。这些发现似乎独立于利拉鲁肽对糖代谢的已知作用。