Effects of chronic exercise on endothelial dysfunction and insulin signaling of cutaneous microvascular in streptozotocin-induced diabetic rats
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Heidarianpour, Ali
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Tarbiat Modares Univ, Dept Physiol, Sch Med Sci, Fac Med Sci, Tehran, IranTarbiat Modares Univ, Dept Physiol, Sch Med Sci, Fac Med Sci, Tehran, Iran
Heidarianpour, Ali
[1
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Hajizadeh, Sohrab
[1
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Khoshbaten, Ali
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Baghiyatallah Med Sci Univ, Dept Physiol, Tehran, IranTarbiat Modares Univ, Dept Physiol, Sch Med Sci, Fac Med Sci, Tehran, Iran
Khoshbaten, Ali
[2
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Niaki, Abbas Ghanbari
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Tarbiat Modares Univ, Dept Phys Educ & Sport Sci, Tehran, IranTarbiat Modares Univ, Dept Physiol, Sch Med Sci, Fac Med Sci, Tehran, Iran
Niaki, Abbas Ghanbari
[3
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Bigdili, Mohammad Reza
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Tarbiat Modares Univ, Dept Physiol, Sch Med Sci, Fac Med Sci, Tehran, IranTarbiat Modares Univ, Dept Physiol, Sch Med Sci, Fac Med Sci, Tehran, Iran
Bigdili, Mohammad Reza
[1
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Pourkhalili, Khalil
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Tarbiat Modares Univ, Dept Physiol, Sch Med Sci, Fac Med Sci, Tehran, IranTarbiat Modares Univ, Dept Physiol, Sch Med Sci, Fac Med Sci, Tehran, Iran
Pourkhalili, Khalil
[1
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[1] Tarbiat Modares Univ, Dept Physiol, Sch Med Sci, Fac Med Sci, Tehran, Iran
[2] Baghiyatallah Med Sci Univ, Dept Physiol, Tehran, Iran
Background Abnormalities of the modulatory roles played by the endothelium and/or smooth muscle may be critical and initiating factors in the development of diabetic vascular disease. Decreased phosphatidylinositol 3-kinase (PI3-K)/Akt pathway activity and impaired nitric oxide production through this pathway may play pivotal roles in the diabetes-induced vascular dysfunction. Several findings have demonstrated that exercise training has therapeutic and protective effects in type 1 diabetes and could correct endothelial dysfunction. The molecular mechanisms, however, are only partially understood. Method Male Wistar rats (220 10 g, N= 60) were made diabetic by streptozotocin (60 mg/kg, subcutaneously). After 1 week of diabetes induction, animals were submitted to exercise training for 10 weeks on a treadmill. To characterize cutaneous microvascular responses by laser Doppler flowmetery, animals were deeply anesthetized by intraperitoneal injection of pentobarbital sodium (60 mg/kg) and placed on a heating pad. A rectal thermometer was inserted and body temperature was maintained at 37 +/- 0.5 degrees C. A tracheotomy was performed to minimize respiratory difficulties. Systemic arterial blood pressure and heart rate were measured by using a tail-cuff during assessment of cutaneous blood flow. Results 0) Acetylcholine-induced cutaneous perfusion were increased significantly by training in the diabetic groups; (ii) Cutaneous microvascular responses to sodium nitroprusside did not alter in control and diabetic animals by training; and NO Local microinjection of insulin increased cutaneous blood flow in trained diabetic and trained control rats compared with age-matched sedentary diabetic and sedentary control normal rats. The administration of wortmannin (PI3K inhibitor) and N-w-nitro-L-arginine (nitric oxide synthase inhibitor) before insulin, however, attenuated the increase in cutaneous blood flow in trained diabetic and normal rats. Conclusions Chronic exercise improved endothelium-dependent dilatation and potentiated insulin vascular function, possibly by P13-kinase pathway in diabetic rats. Eur J Cardiovasc Prev Rehabil 14:746-752 (c) 2007.
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Hoshi Univ, Inst Med Chem, Dept Phys & Morphol, Shinagawa Ku, Tokyo 1428501, JapanHoshi Univ, Inst Med Chem, Dept Phys & Morphol, Shinagawa Ku, Tokyo 1428501, Japan
Matsumoto, T
Yoshiyama, S
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Hoshi Univ, Inst Med Chem, Dept Phys & Morphol, Shinagawa Ku, Tokyo 1428501, JapanHoshi Univ, Inst Med Chem, Dept Phys & Morphol, Shinagawa Ku, Tokyo 1428501, Japan
Yoshiyama, S
Wakabayashi, K
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Hoshi Univ, Inst Med Chem, Dept Phys & Morphol, Shinagawa Ku, Tokyo 1428501, JapanHoshi Univ, Inst Med Chem, Dept Phys & Morphol, Shinagawa Ku, Tokyo 1428501, Japan
Wakabayashi, K
Kobayashi, T
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Hoshi Univ, Inst Med Chem, Dept Phys & Morphol, Shinagawa Ku, Tokyo 1428501, JapanHoshi Univ, Inst Med Chem, Dept Phys & Morphol, Shinagawa Ku, Tokyo 1428501, Japan
Kobayashi, T
Kamata, K
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Hoshi Univ, Inst Med Chem, Dept Phys & Morphol, Shinagawa Ku, Tokyo 1428501, JapanHoshi Univ, Inst Med Chem, Dept Phys & Morphol, Shinagawa Ku, Tokyo 1428501, Japan