Bromocriptine enhances the uptake of 99mTc-MIBI in patients with hepatocellular carcinoma
99mTc-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...
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2012
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pubmed-35960662013-04-02 Bromocriptine enhances the uptake of 99mTc-MIBI in patients with hepatocellular carcinoma Chai, Xiangting Liu, Qiaoyu Shao, Wenyu Zhang, Feng Wang, Xuehao Wang, Hai Research Paper 99mTc-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 99mTc-MIBI imaging. In the current study, we sought to investigate whether bromocriptine enhanced the uptake of 99mTc-MIBI in hepatocellular carcinoma patients. Sixty primary hepatocellular carcinoma patients received 99mTc-MIBI single photon emission computer tomgraphy (SPECT) prior to surgery. 99mTc-MIBI SPECT was performed 15 and 120 min after injection of 20 mCi 99mTc-MIBI, and early uptake, delayed uptake (L/Nd), and washout rate (L/Nwr) of 99mTc-MIBI were obtained. In addition, a second 99mTc-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 99mTc-MIBI SPECT (P < 0.05). Our findings indicate that bromocriptine enhances the uptake of 99mTc-MIBI in patients with hepatocellular carcinoma. Editorial Department of Journal of Biomedical Research 2012-05 2012-04-12 /pmc/articles/PMC3596066/ /pubmed/23554746 http://dx.doi.org/10.7555/JBR.26.20110075 Text en © 2012 by the Journal of Biomedical Research. All rights reserved. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
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NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Chai, Xiangting Liu, Qiaoyu Shao, Wenyu Zhang, Feng Wang, Xuehao Wang, Hai |
spellingShingle |
Chai, Xiangting Liu, Qiaoyu Shao, Wenyu Zhang, Feng Wang, Xuehao Wang, Hai Bromocriptine enhances the uptake of 99mTc-MIBI in patients with hepatocellular carcinoma |
author_facet |
Chai, Xiangting Liu, Qiaoyu Shao, Wenyu Zhang, Feng Wang, Xuehao Wang, Hai |
author_sort |
Chai, Xiangting |
title |
Bromocriptine enhances the uptake of 99mTc-MIBI in patients with hepatocellular carcinoma |
title_short |
Bromocriptine enhances the uptake of 99mTc-MIBI in patients with hepatocellular carcinoma |
title_full |
Bromocriptine enhances the uptake of 99mTc-MIBI in patients with hepatocellular carcinoma |
title_fullStr |
Bromocriptine enhances the uptake of 99mTc-MIBI in patients with hepatocellular carcinoma |
title_full_unstemmed |
Bromocriptine enhances the uptake of 99mTc-MIBI in patients with hepatocellular carcinoma |
title_sort |
bromocriptine enhances the uptake of 99mtc-mibi in patients with hepatocellular carcinoma |
description |
99mTc-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 99mTc-MIBI imaging. In the current study, we sought to investigate whether bromocriptine enhanced the uptake of 99mTc-MIBI in hepatocellular carcinoma patients. Sixty primary hepatocellular carcinoma patients received 99mTc-MIBI single photon emission computer tomgraphy (SPECT) prior to surgery. 99mTc-MIBI SPECT was performed 15 and 120 min after injection of 20 mCi 99mTc-MIBI, and early uptake, delayed uptake (L/Nd), and washout rate (L/Nwr) of 99mTc-MIBI were obtained. In addition, a second 99mTc-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 99mTc-MIBI SPECT (P < 0.05). Our findings indicate that bromocriptine enhances the uptake of 99mTc-MIBI in patients with hepatocellular carcinoma. |
publisher |
Editorial Department of Journal of Biomedical Research |
publishDate |
2012 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596066/ |
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1611961655113023488 |