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溴隐亭可增强肝细胞癌患者对(99m)Tc-MIBI的摄取。

Bromocriptine enhances the uptake of (99m)Tc-MIBI in patients with hepatocellular carcinoma.

作者信息

Chai Xiangting, Liu Qiaoyu, Shao Wenyu, Zhang Feng, Wang Xuehao, Wang Hai

机构信息

Department of Internal Medicine, Jiaonan People's Hospital of Shandong Province, Jiaonan, Shandong 266400, China;

出版信息

J Biomed Res. 2012 May;26(3):165-9. doi: 10.7555/JBR.26.20110075. Epub 2012 Apr 12.

DOI:10.7555/JBR.26.20110075
PMID:23554746
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3596066/
Abstract

(99m)Tc-methoxyisobutyl isonitrile (MIBI) is a suitable transport substrate for the multidrug resistance gene product P-glycoprotein (P-gp) and widely used for tumor imaging. Bromocriptine has been shown to inhibit the ATPase activity and the function of P-gp. We hypothesized that bromocriptine could promote the accumulation of MIBI by inhibiting P-gp activities, a feature that can be taken advantage of for enhancing (99m)Tc-MIBI imaging. In the current study, we sought to investigate whether bromocriptine enhanced the uptake of (99m)Tc-MIBI in hepatocellular carcinoma patients. Sixty primary hepatocellular carcinoma patients received (99m)Tc-MIBI single photon emission computer tomgraphy (SPECT) prior to surgery. (99m)Tc-MIBI SPECT was performed 15 and 120 min after injection of 20 mCi (99m)Tc-MIBI, and early uptake, delayed uptake (L/Nd), and washout rate (L/Nwr) of (99m)Tc-MIBI were obtained. In addition, a second (99m)Tc-MIBI SPECT was performed according to the same method 48 h after bromocriptine administration. We found that, prior to bromocriptine administration, significant MIBI uptake in tumor lesions was noted in only 10 (16.7%, 10/60) patients with hepatocellular carcinoma. No significant MIBI uptake was observed in the tumor lesions of the remaining 50 (83.3%, 50/60) hepatocellular carcinoma patients. Following bromocriptine administration, all the patients without apparent MIBI uptake demonstrated significant MIBI uptake on (99m)Tc-MIBI SPECT (P < 0.05). Our findings indicate that bromocriptine enhances the uptake of (99m)Tc-MIBI in patients with hepatocellular carcinoma.

摘要

锝-99m甲氧基异丁基异腈(MIBI)是多药耐药基因产物P-糖蛋白(P-gp)合适的转运底物,广泛用于肿瘤显像。已证实溴隐亭可抑制P-gp的ATP酶活性及其功能。我们推测溴隐亭可通过抑制P-gp活性促进MIBI的蓄积,这一特性可用于增强锝-99m MIBI显像。在本研究中,我们试图探讨溴隐亭是否能增强肝细胞癌患者对锝-99m MIBI的摄取。60例原发性肝细胞癌患者在手术前行锝-99m MIBI单光子发射计算机断层扫描(SPECT)。静脉注射20 mCi锝-99m MIBI后15分钟和120分钟行锝-99m MIBI SPECT检查,获得锝-99m MIBI的早期摄取、延迟摄取(L/Nd)和洗脱率(L/Nwr)。此外,在给予溴隐亭48小时后,按照相同方法再次行锝-99m MIBI SPECT检查。我们发现,在给予溴隐亭之前,仅10例(16.7%,10/60)肝细胞癌患者的肿瘤病灶有明显的MIBI摄取。其余50例(83.3%,50/60)肝细胞癌患者的肿瘤病灶未观察到明显的MIBI摄取。给予溴隐亭后,所有未出现明显MIBI摄取的患者在锝-99m MIBI SPECT上均显示出明显的MIBI摄取(P<0.05)。我们的研究结果表明,溴隐亭可增强肝细胞癌患者对锝-99m MIBI的摄取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86f6/3596066/a4d3105d27d7/jbr-26-03-165-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86f6/3596066/a4d3105d27d7/jbr-26-03-165-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86f6/3596066/a4d3105d27d7/jbr-26-03-165-g001.jpg

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