Antihypertensive Action of Allantoin in Animals

被引:26
作者
Chen, Mei-Fen [1 ,2 ]
Tsai, Jo-Ting [3 ,4 ]
Chen, Li-Jen [5 ]
Wu, Tung-Pi [6 ]
Yang, Jia-Jang [2 ]
Yin, Li-Te [2 ]
Yang, Yu-lin [2 ]
Chiang, Tai-An [2 ]
Lu, Han-Lin [7 ]
Wu, Ming-Chang [1 ]
机构
[1] Natl Pingtung Univ Sci & Technol, Dept Food Sci, Pingtung City 91201, Taiwan
[2] Chung Hwa Univ Med Technol, Coll Med & Life Sci, Tainan 71703, Taiwan
[3] Taipei Med Univ, Shuang Ho Hosp, Dept Radiat Oncol, Taipei 10361, Taiwan
[4] Taipei Med Univ, Coll Med, Taipei 10361, Taiwan
[5] Natl Cheng Kung Univ, Inst Basic Med Sci, Coll Med, Tainan 70101, Taiwan
[6] Tainan SinLau Hosp, Dept Obs Gyn, Presbyterian Church Taiwan, Tainan 70142, Taiwan
[7] Tainan SinLau Hosp, Dept Chinese Med, Presbyterian Church Taiwan, Tainan 70142, Taiwan
关键词
IMIDAZOLINE I-1 RECEPTORS; PLASMA-GLUCOSE; DIOSCOREA; TARGETS; DRUGS; ACTIVATION; MOXONIDINE; CLONIDINE; EXCRETION; PATHWAY;
D O I
10.1155/2014/690135
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The agonists of imidazoline I-1 receptors (I-1R) are widely used to lower blood pressure. It has been indicated that guanidinium derivatives show an ability to activate imidazoline receptors. Also, allantoin has a chemical stricture similar to guanidinium derivatives. Thus, it is of special interest to characterize the effect of allantoin on I-1R. In conscious male spontaneous hypertensive rats (SHRs), mean blood pressure (MBP) was recorded using the tail-cuff method. Furthermore, the hemodynamic analyses in catheterized rats were applied to measure the actions of allantoin in vivo. Allantoin decreased blood pressures in SHRs at 30 minutes, as the most effective time. Also, this antihypertensive action was shown in a dose-dependent manner from SHRs treated with allantoin. Moreover, in anesthetized rats, allantoin inhibited cardiac contractility and heart rate as showing in hemodynamic dP/dt max significantly. Also, the peripheral blood flow was markedly increased by allantoin. Both actions were diminished by efaroxan at the dose sufficient to block I-1R. Thus, we suggest that allantoin, as I-1R agonist, has the potential to develop as a new therapeutic agent for hypertension in the future.
引用
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页数:6
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