Synthesis and biological evaluation of an 111In-labeled exendin-4 derivative as a single-photon emission computed tomography probe for imaging pancreatic β-cells. Issue 20 (15th October 2017)
- Record Type:
- Journal Article
- Title:
- Synthesis and biological evaluation of an 111In-labeled exendin-4 derivative as a single-photon emission computed tomography probe for imaging pancreatic β-cells. Issue 20 (15th October 2017)
- Main Title:
- Synthesis and biological evaluation of an 111In-labeled exendin-4 derivative as a single-photon emission computed tomography probe for imaging pancreatic β-cells
- Authors:
- Kimura, Hiroyuki
Fujita, Naotaka
Kanbe, Kaori
Matsuda, Hirokazu
Watanabe, Hiroyuki
Arimitsu, Kenji
Fujimoto, Hiroyuki
Hamamatsu, Keita
Yagi, Yusuke
Ono, Masahiro
Inagaki, Nobuya
Saji, Hideo - Abstract:
- Graphical abstract: Abstract: A non-invasive method of pancreatic β-cell mass measurement is needed to enhance our understanding of the pathogenesis of diabetes, facilitate the early diagnosis of this disease, and promote the development of novel therapeutics. Here, we described the synthesis of a novel indium-111 ( 111 In) exendin-4 derivative, [Lys 12 (In-BnDTPA-Ahx)]exendin-4, through a process involving isothiocyanate-benzyl-DTPA (BnDTPA) and 6-aminohexanoic acid (Ahx) attached to an ɛ-amino group at the lysine-12 residue. We further evaluated the potential use of this derivative as a SPECT probe for pancreatic β-cell imaging. An in vitro binding assay revealed that [Lys 12 ( nat In-BnDTPA-Ahx)]exendin-4 has a high affinity for GLP-1 receptors (IC50 = 0.43 nM). In biodistribution experiments involving normal mice, high [Lys 12 ( 111 In-BnDTPA-Ahx)]exendin-4 uptake was observed in the pancreas (21.8 ± 4.0 %ID/g) and was maintained for 2 h after injection. Pre-injection of excess exendin(9−39) markedly reduced the pancreatic uptake of [Lys 12 ( 111 In-BnDTPA-Ahx)]exendin-4 (95.2%), indicating that the uptake of this tracer is specific and mediated by GLP-1 receptors. Ex vivo autoradiography experiments involving pancreatic sections from MIP-GFP mice confirmed the accumulation of [Lys 12 ( 111 In-BnDTPA-Ahx)]exendin-4 in pancreatic β-cells. Finally, in mice, [Lys 12 ( 111 In-BnDTPA-Ahx)]exendin-4 SPECT/CT yielded clear images of the pancreas at 30 min post-injection. InGraphical abstract: Abstract: A non-invasive method of pancreatic β-cell mass measurement is needed to enhance our understanding of the pathogenesis of diabetes, facilitate the early diagnosis of this disease, and promote the development of novel therapeutics. Here, we described the synthesis of a novel indium-111 ( 111 In) exendin-4 derivative, [Lys 12 (In-BnDTPA-Ahx)]exendin-4, through a process involving isothiocyanate-benzyl-DTPA (BnDTPA) and 6-aminohexanoic acid (Ahx) attached to an ɛ-amino group at the lysine-12 residue. We further evaluated the potential use of this derivative as a SPECT probe for pancreatic β-cell imaging. An in vitro binding assay revealed that [Lys 12 ( nat In-BnDTPA-Ahx)]exendin-4 has a high affinity for GLP-1 receptors (IC50 = 0.43 nM). In biodistribution experiments involving normal mice, high [Lys 12 ( 111 In-BnDTPA-Ahx)]exendin-4 uptake was observed in the pancreas (21.8 ± 4.0 %ID/g) and was maintained for 2 h after injection. Pre-injection of excess exendin(9−39) markedly reduced the pancreatic uptake of [Lys 12 ( 111 In-BnDTPA-Ahx)]exendin-4 (95.2%), indicating that the uptake of this tracer is specific and mediated by GLP-1 receptors. Ex vivo autoradiography experiments involving pancreatic sections from MIP-GFP mice confirmed the accumulation of [Lys 12 ( 111 In-BnDTPA-Ahx)]exendin-4 in pancreatic β-cells. Finally, in mice, [Lys 12 ( 111 In-BnDTPA-Ahx)]exendin-4 SPECT/CT yielded clear images of the pancreas at 30 min post-injection. In conclusion, SPECT with [Lys 12 ( 111 In-BnDTPA-Ahx)]exendin-4 enables to visualize β-cells in vivo non-invasively. … (more)
- Is Part Of:
- Bioorganic & medicinal chemistry. Volume 25:Issue 20(2017)
- Journal:
- Bioorganic & medicinal chemistry
- Issue:
- Volume 25:Issue 20(2017)
- Issue Display:
- Volume 25, Issue 20 (2017)
- Year:
- 2017
- Volume:
- 25
- Issue:
- 20
- Issue Sort Value:
- 2017-0025-0020-0000
- Page Start:
- 5772
- Page End:
- 5778
- Publication Date:
- 2017-10-15
- Subjects:
- BCM beta cell mass -- DTBZ dihydrotetrabenazine -- DTPA diethylenetriamine-pentaacetic acid -- GFP green fluorescent protein -- GLP-1 glucagon-like peptide-1 -- MIP mouse insulin I gene promotor -- NOD 1-(1, 3-carboxypropyl)-1, 4, 7-triazacyclononane-4, 7-diacetic acid -- PET positron emission tomography -- RP-HPLC reverse-phase high-performance liquid chromatography -- SPECT single-photon emission computed tomography -- VMAT2 vesicular monoamine transporter 2
Exendin4 -- Single-photon emission computed tomography -- 111Indium -- Glucagon-like peptide 1 receptor -- Pancreatic β-cell imaging
Bioorganic chemistry -- Periodicals
Pharmaceutical chemistry -- Periodicals
Biochemistry -- Periodicals
Chemistry, Clinical -- Periodicals
Chemistry, Organic -- Periodicals
Chimie bio-organique -- Périodiques
Chimie pharmaceutique -- Périodiques
615.19 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09680896 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.bmc.2017.09.005 ↗
- Languages:
- English
- ISSNs:
- 0968-0896
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2089.325000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10724.xml