[3H]坦索罗辛对人肥大前列腺中α 1肾上腺素受体的定量放射自显影分析。

The Histochemical Journal Pub Date : 1995-12-01
S Kurimoto, N Moriyama, K Hamada, J Taniguchi, K Kawabe
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引用次数: 0

摘要

采用计算机图像分析系统的放射自显影技术对14例人前列腺肥大患者的α 1肾上腺素受体分布进行了评价。在开放性前列腺切除术中获得的肥大前列腺标本,垂直于尿道解剖,并在10微米处切片。将它们浸泡在1 nM的特异性α - 1配体[3H]坦索罗辛氯([3H]坦索罗辛)中,并暴露于放射自显影膜中。通过计算机图像分析系统对图像进行分析。整个切片(n = 14) [3H]坦索罗辛的总结合量为0.82 +/- 0.21(平均+/- SE) nCi mg-1。自体数据与膜结合试验中获得的数据相关。所研究的前列腺组织分为尿道区、腺区和间质区,后两个区又分为内区和外区。[3H]坦索罗辛在尿道区(n = 7)的总结合量为0.65±0.32 nCi mg-1。腺区α -1肾上腺素受体含量显著高于间质区,其密度(腺区与间质区)分别为1.15 +/- 0.19 nCi mg-1 (n = 14)和0.72 +/- 0.15 nCi mg-1 (n = 14) (p < 0.05)。整个切片的数据不受前列腺重量的影响。所描述的这种方法使受体在不同部位的分布可以进行形态学和定量的评估。
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Quantitative autoradiography of alpha 1 adrenoceptors with [3H]tamsulosin in human hypertrophied prostate using computerized image analysis.

Fourteen specimens of human hypertrophied prostate were evaluated for the distribution of alpha 1 adrenoceptors using autoradiography with a computerized image analysis system. The hypertrophied prostatic specimens, obtained at open prostatectomy, were dissected vertically to the urethra, and sectioned at 10 microns. They were immersed in 1 nM of specific alpha 1 ligand, [3H]tamsulosin chloride ([3H]tamsulosin) and exposed to autoradiographic film. The images were analysed by a computerized image analysis system. The total binding of [3H]tamsulosin in the whole section (n = 14) was 0.82 +/- 0.21 (mean +/- SE) nCi mg-1. The autographic data were correlated with data obtained in a membrane-binding assay. The prostatic tissue studied was divided into urethral, glandular and stromal zones, the latter two zones being further divided into the inner and outer areas. The total binding of [3H]tamsulosin in the urethral zone (n = 7) was 0.65 +/- 0.32 nCi mg-1. The glandular zone contained significantly more abundant alpha 1 adrenoceptors than the stromal zone and their densities (glandular vs stromal) were 1.15 +/- 0.19 nCi mg-1 (n = 14) vs 0.72 +/- 0.15 nCi mg-1 (n = 14), respectively (p < 0.05). The data from the whole section were not affected by prostatic weight. This method described enabled the distribution of the receptors in different sites to be evaluated both morphologically and quantitatively.

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