Bialik G M, Abassi Z A, Hammel I, Winaver J, Lewinson D
Department of Anatomy and Cell Biology, The Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
J Histochem Cytochem. 2001 Oct;49(10):1293-300. doi: 10.1177/002215540104901012.
The natriuretic peptides are believed to play an important role in the pathophysiology of congestive heart failure (CHF). We utilized a quantitative cytomorphometric method, using double immunocytochemical labeling, to assess the characteristics of atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) in atrial granules in an experimental model of rats with CHF induced by aortocaval fistula. Rats with CHF were further divided into decompensated (sodium-retaining) and compensated (sodium-excreting) subgroups and compared with a sham-operated control group. A total of 947 granules in myocytes in the right atrium were analyzed, using electron microscopy and a computerized analysis system. Decompensated CHF was associated with alterations in the modal nature of granule content packing, as depicted by moving bin analysis, and in the granule density of both peptides. In control rats, the mean density of gold particles attached to both peptides was 347.0 +/- 103.6 and 306.3 +/- 89.9 gold particles/microm2 for ANP and BNP, respectively. Similar mean density was revealed in the compensated rats (390.6 +/- 81.0 and 351.3 +/- 62.1 gold particles/microm2 for ANP and BNP, respectively). However, in rats with decompensated CHF, a significant decrease in the mean density of gold particles was observed (141.6 +/- 67.3 and 158.0 +/- 71.2 gold particles/microm2 for ANP and BNP, respectively; p<0.05 compared with compensated rats, for both ANP and BNP). The ANP:BNP ratio did not differ between groups. These findings indicate that the development of decompensated CHF in rats with aortocaval fistula is associated with a marked decrease in the density of both peptides in atrial granules, as well as in alterations in the quantal nature of granule formation. The data further suggest that both peptides, ANP and BNP, may be regulated in the atrium by a common secretory mechanism in CHF.
利钠肽被认为在充血性心力衰竭(CHF)的病理生理学中起重要作用。我们采用定量细胞形态计量学方法,通过双重免疫细胞化学标记,来评估在主动脉腔静脉瘘诱导的CHF大鼠实验模型中,心房颗粒中心房利钠肽(ANP)和脑利钠肽(BNP)的特征。CHF大鼠进一步分为失代偿(钠潴留)和代偿(钠排泄)亚组,并与假手术对照组进行比较。使用电子显微镜和计算机分析系统,对右心房肌细胞中的总共947个颗粒进行了分析。失代偿性CHF与颗粒内容物堆积的模态性质改变(通过移动箱分析描绘)以及两种肽的颗粒密度改变有关。在对照大鼠中,与ANP和BNP结合的金颗粒的平均密度分别为347.0±103.6和306.3±89.9金颗粒/μm²。在代偿大鼠中也观察到类似的平均密度(ANP和BNP分别为390.6±81.0和351.3±62.1金颗粒/μm²)。然而,在失代偿性CHF大鼠中,观察到金颗粒的平均密度显著降低(ANP和BNP分别为141.6±67.3和158.0±71.2金颗粒/μm²;与代偿大鼠相比,ANP和BNP均p<0.05)。各组之间ANP:BNP比值无差异。这些发现表明,主动脉腔静脉瘘大鼠失代偿性CHF的发展与心房颗粒中两种肽的密度显著降低以及颗粒形成的量子性质改变有关。数据进一步表明,在CHF中,ANP和BNP这两种肽可能在心房中通过共同的分泌机制受到调节。