Noninvasive longitudinal quantification of β‐cell mass with [111In]‐labeled exendin‐4. Issue 11 (1st August 2019)
- Record Type:
- Journal Article
- Title:
- Noninvasive longitudinal quantification of β‐cell mass with [111In]‐labeled exendin‐4. Issue 11 (1st August 2019)
- Main Title:
- Noninvasive longitudinal quantification of β‐cell mass with [111In]‐labeled exendin‐4
- Authors:
- Fujita, Naotaka
Fujimoto, Hiroyuki
Hamamatsu, Keita
Murakami, Takaaki
Kimura, Hiroyuki
Toyoda, Kentaro
Saji, Hideo
Inagaki, Nobuya - Abstract:
- Abstract : Currently, quantifying β‐cell mass (BCM) requires harvesting the pancreas. In this study, we investigated a potential noninvasive method to quantify BCM changes longitudinally using [Lys 12 ( 111 In‐BnDTPA‐Ahx)] exendin‐4 ([ 111 In]‐Ex4) and single‐photon emission computed tomography (SPECT). We used autoradiography and transgenic mice expressing green fluorescent protein under the control of mouse insulin 1 gene promotor to evaluate the specificity of [ 111 In]‐Ex4 toward β cells. Using nonobese diabetic (NOD) mice, we injected [ 111 In]‐Ex4 (3.0 MBq) intravenously and performed SPECT 30 min later, repeating this at a 2‐wk interval. After the second scan, we harvested the pancreas and calculated BCM from immunohistochemically stained pancreatic sections. Specific accumulation of [ 111 In]‐Ex4 in β cells was confirmed by autoradiography, with a significant correlation ( r = 0.94) between the fluorescent and radioactive signal intensities. The radioactive signal from the pancreas in the second SPECT scan significantly correlated ( r = 0.89) with BCM calculated from the immunostained pancreatic sections. We developed a regression formula to estimate BCM from the radioactive signals from the pancreas in SPECT scans. BCM can be quantified longitudinally and noninvasively by SPECT imaging with [ 111 In]‐Ex4. This technique successfully demonstrated longitudinal changes in BCM in NOD mice before and after onset of hyperglycemia.—Fujita, N., Fujimoto, H., Hamamatsu, K.,Abstract : Currently, quantifying β‐cell mass (BCM) requires harvesting the pancreas. In this study, we investigated a potential noninvasive method to quantify BCM changes longitudinally using [Lys 12 ( 111 In‐BnDTPA‐Ahx)] exendin‐4 ([ 111 In]‐Ex4) and single‐photon emission computed tomography (SPECT). We used autoradiography and transgenic mice expressing green fluorescent protein under the control of mouse insulin 1 gene promotor to evaluate the specificity of [ 111 In]‐Ex4 toward β cells. Using nonobese diabetic (NOD) mice, we injected [ 111 In]‐Ex4 (3.0 MBq) intravenously and performed SPECT 30 min later, repeating this at a 2‐wk interval. After the second scan, we harvested the pancreas and calculated BCM from immunohistochemically stained pancreatic sections. Specific accumulation of [ 111 In]‐Ex4 in β cells was confirmed by autoradiography, with a significant correlation ( r = 0.94) between the fluorescent and radioactive signal intensities. The radioactive signal from the pancreas in the second SPECT scan significantly correlated ( r = 0.89) with BCM calculated from the immunostained pancreatic sections. We developed a regression formula to estimate BCM from the radioactive signals from the pancreas in SPECT scans. BCM can be quantified longitudinally and noninvasively by SPECT imaging with [ 111 In]‐Ex4. This technique successfully demonstrated longitudinal changes in BCM in NOD mice before and after onset of hyperglycemia.—Fujita, N., Fujimoto, H., Hamamatsu, K., Murakami, T., Kimura, H., Toyoda, K., Saji, H., Inagaki, N. Noninvasive longitudinal quantification of β‐cell mass with [ 111 In]‐labeled exendin‐4. FASEB J. 33, 11836‐11844 (2019). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 33:Issue 11(2019)
- Journal:
- FASEB journal
- Issue:
- Volume 33:Issue 11(2019)
- Issue Display:
- Volume 33, Issue 11 (2019)
- Year:
- 2019
- Volume:
- 33
- Issue:
- 11
- Issue Sort Value:
- 2019-0033-0011-0000
- Page Start:
- 11836
- Page End:
- 11844
- Publication Date:
- 2019-08-01
- Subjects:
- in vivo radioisotope -- GLP‐1 receptor -- SPECT
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201900555RR ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23879.xml