The association of nitric oxide (NO) with the hypotensive effects of adrenomedullin (AM) was investigated in anesthetized rats. Spontaneously hypertensive rats (SHR) and normotensive Wistar Kyoto rats (WKY) were used at 11-13 weeks of age. Blood pressure and heart rate were measured from the femoral
Nitric oxide-associated relaxing effects of adrenomedullin in rat aorta
โ Scribed by Kazuki Matsunaga; Takanori Iwasaki; Yukio Yonetani; Kazuo Kitamura; Tanenao Eto; Kenji Kangawa; Hisayuki Matsuo
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 402 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0272-4391
No coin nor oath required. For personal study only.
โฆ Synopsis
The relaxing effect of adrenomedullin (AM) and that associated with nitric oxide (NO) were investigated in rat isolated aorta. The relaxing effect produced by AM was almost completely inhibited by the removal of endothelium and by treatment with the NOS inhibitor fl-nitro-L-arginine methyester (L-NAME) and hemoglobin but not by indomethacin. Thus the relaxing effect by AM was entirely dependent of endothelial NO synthesis but not of prostaglandins. The cGMP content in t h e AM-treated relaxed aorta did not change while the cAMP content significantly increased. These findings suggest that the relaxing effects produced by AM in rat aorta primarily relate to an increase in cAMP as well as cGMP maintained by the stimulation of NO spontaneously released from endothelium but not by cGMP resulting from enhanced NO release. There may be some synergistic mechanism between cAMP and NO-cGMP systems in the relaxing effect of AM in rat isolated aorta. o 19% Wiley-Liss, Inc.
๐ SIMILAR VOLUMES
## Background: The presence of nitric-oxide-synthesising neurons in the adrenal gland has recently been described by the immunohistochemical and/or enzyme histochemical demonstration of its synthesising enzyme, nitric oxide synthase (nos; afework et al. 1994. cell tissue res,276:133-141). in the pr
Kupffer cells play important roles in the development of liver injury by producing cytokines and free radicals. In consequence inhibition of these inflammatory mediators will be one of the targets for treating liver diseases. Retinoids modulate a wide variety of functions of monocytes/macrophages. C