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氨基酸输注可阻断肾小管对铟标记的生长抑素类似物的摄取。

Amino acid infusion blocks renal tubular uptake of an indium-labelled somatostatin analogue.

作者信息

Hammond P J, Wade A F, Gwilliam M E, Peters A M, Myers M J, Gilbey S G, Bloom S R, Calam J

机构信息

Department of Medicine, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.

出版信息

Br J Cancer. 1993 Jun;67(6):1437-9. doi: 10.1038/bjc.1993.266.

DOI:10.1038/bjc.1993.266
PMID:8099808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1968533/
Abstract

The Indium-labelled somatostatin analogue pentetreotide has been successfully developed for imaging of somatostatin receptor positive tumours. However there is significant renal tubular uptake of the radiolabelled peptide, which can obscure upper abdominal tumours and would preclude its use for targeted radiotherapy. The aim of this study was to determine whether amino acid infusion, which has been shown to block renal tubular peptide reabsorption, diminishes renal parenchymal uptake of this radiolabelled analogue. Eight patients being scanned with the 111In-labelled somatostatin analogue, pentetreotide, for localisation of gastroenteropancreatic tumours received an infusion of synthetic amino acids. The ratio of isotope uptake in kidney to that in spleen was assessed, and compared to the ratio for matched control patients, to determine if amino acid infusion reduced renal parenchymal uptake of the radiopharmaceutical. The amount of isotope in the urine was determined to ensure that any effect of the amino acid infusion was unrelated to changes in clearance. Infusion of amino acids significantly reduced renal parenchymal uptake of isotope at 4 h. There was a non-significant increase in urinary clearance of isotope over the 4 h, consistent with reduced reuptake and a lack of effect on glomerular filtration rate. This technique, by preventing renal damage, may allow the use of this somatostatin analogue for local radiotherapy, and could be of wider value in blocking tubular re-uptake of potentially nephrotoxic agents, such as radiolabelled Fab fragments.

摘要

铟标记的生长抑素类似物喷曲肽已成功用于生长抑素受体阳性肿瘤的成像。然而,放射性标记的肽在肾小管有显著摄取,这可能会掩盖上腹部肿瘤,并使其无法用于靶向放疗。本研究的目的是确定已被证明能阻断肾小管肽重吸收的氨基酸输注是否会减少这种放射性标记类似物在肾实质的摄取。8例接受铟-111标记的生长抑素类似物喷曲肽扫描以定位胃肠胰肿瘤的患者接受了合成氨基酸输注。评估肾脏与脾脏的同位素摄取比值,并与匹配的对照患者的比值进行比较,以确定氨基酸输注是否降低了放射性药物在肾实质的摄取。测定尿液中的同位素量,以确保氨基酸输注的任何影响与清除率的变化无关。氨基酸输注在4小时时显著降低了同位素在肾实质的摄取。在4小时内,同位素的尿清除率有不显著的增加,这与重吸收减少和对肾小球滤过率无影响一致。通过防止肾损伤,这种技术可能允许使用这种生长抑素类似物进行局部放疗,并且在阻断潜在肾毒性药物(如放射性标记的Fab片段)的肾小管重吸收方面可能具有更广泛的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9480/1968533/ad6099cd55ed/brjcancer00208-0278-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9480/1968533/ad6099cd55ed/brjcancer00208-0278-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9480/1968533/ad6099cd55ed/brjcancer00208-0278-a.jpg

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