Exendin-4 has an anti-hypertensive effect in salt-sensitive mice model

被引:163
作者
Hirata, Kunio [1 ]
Kume, Shinji [1 ]
Araki, Shin-ichi [1 ]
Sakaguchi, Masayoshi [1 ]
Chin-Kanasaki, Masami [1 ]
Isshiki, Keiji [1 ]
Sugimoto, Toshiro [1 ]
Nishiyama, Akira [2 ]
Koya, Daisuke [3 ]
Haneda, Masakazu [4 ]
Kashiwagi, Atsunori [1 ]
Uzu, Takashi [1 ]
机构
[1] Shiga Univ Med Sci, Dept Med, Shiga 5202192, Japan
[2] Kagawa Univ, Dept Pharmacol, Kagawa, Japan
[3] Kanazawa Med Univ, Div Endocrinol & Metab, Kanazawa, Ishikawa, Japan
[4] Asahikawa Med Coll, Dept Med, Asahikawa, Hokkaido 078, Japan
关键词
Angiotensin II; db/db mice; Diabetic nephropathy; Exendin-4; GLP-1; receptor; Renin-angiotensin system; Salt-sensitivity; Hypertension; Type; 2; diabetes; GLUCAGON-LIKE PEPTIDE-1; HIGH-FAT DIET; ANGIOTENSIN-II; METABOLIC SYNDROME; BLOOD-PRESSURE; ESSENTIAL-HYPERTENSION; SODIUM SENSITIVITY; MESANGIAL CELLS; DB/DB MICE; RECEPTOR;
D O I
10.1016/j.bbrc.2009.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The improvement of salt-sensitive hypertension is a therapeutic target for various vascular diseases. Glucagon-like peptide 1 (GLP-1), an incretin peptide, has been reported to have natriuretic effect as well as blood glucose lowering effect, although its exact mechanism and clinical usefulness remain unclear. Here, we examined anti-hypertensive effect of exendin-4, a GLP-1 analog, in salt-sensitive obese db/db mice and angiotensin II (angII)-infused C57BLK6/J mice. The treatment of exendin-4 for 12 weeks inhibited the development of hypertension in db/db mice. In db/db mice, the urinary sodium excretion was delayed and blood pressure was elevated in response to a high-salt load, whereas these were attenuated by exendin-4. In db/db mice, intra-renal angII concentration was increased. Furthermore, exendin-4 prevented angII-induced hypertension in non-diabetic mice and inhibited angII-induced phosphorylation of ERK1/2 in cultured renal cells. Considered together, our results indicate that exendin-4 has anti-hypertensive effects through the attenuation of angII-induced high-salt sensitivity. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:44 / 49
页数:6
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