Identification of differentially expressed proteins related to organophosphorus‐induced delayed neuropathy in the brains of hens. Issue 12 (12th December 2013)
- Record Type:
- Journal Article
- Title:
- Identification of differentially expressed proteins related to organophosphorus‐induced delayed neuropathy in the brains of hens. Issue 12 (12th December 2013)
- Main Title:
- Identification of differentially expressed proteins related to organophosphorus‐induced delayed neuropathy in the brains of hens
- Authors:
- Jiang, Ying
Liu, Xiaohui
Li, Shuangyue
Zhang, Yanning
Piao, Fengyuan
Sun, Xiance - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>Some organophosphorus compounds can cause organophosphate‐induced delayed neuropathy (OPIDN). Incidents have been documented for decades, however, little is known about which proteins contribute to the initiation, progression and development of OPIDN. In this study, 51 hens were divided into three groups. The tri‐ortho‐cresyl‐phosphate (TOCP) group was treated with 1000 mg kg<sup>–1</sup> TOCP whereas the control group was treated with an equivalent volume of vehicle. The PMSF + TOCP group was treated subcutaneously with 40 mg kg<sup>–1</sup> phenylmethylsulfonyl fluoride (PMSF), followed by 1000 mg kg<sup>–1</sup> TOCP 24 h later. Proteins in the brains of hens were separated by two‐dimensional polyacrylamide gel electrophoresis on day 5 after TOCP administration. Mass spectrometry identified eight differentially expressed proteins. Among these proteins, downregulated expression of glutamine synthetase (GS) in the brains of hens after TOCP treatment was further confirmed by real time RT‐PCR and ELISA. Moreover, the brains of hens exposed to TOCP exhibited increased levels of glutamate (Glu) and cytosolic calcium concentration ([Ca<sup>2+</sup>]<italic><sub>i</sub></italic>), and a decreased level of glutamine (Gln). However, there were no significant differences in GS expression or levels of Glu, Gln, and [Ca<sup>2+</sup>]<italic><sub>i</sub></italic> in the brains of hens among the groups on day 21 after TOCP<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Some organophosphorus compounds can cause organophosphate‐induced delayed neuropathy (OPIDN). Incidents have been documented for decades, however, little is known about which proteins contribute to the initiation, progression and development of OPIDN. In this study, 51 hens were divided into three groups. The tri‐ortho‐cresyl‐phosphate (TOCP) group was treated with 1000 mg kg<sup>–1</sup> TOCP whereas the control group was treated with an equivalent volume of vehicle. The PMSF + TOCP group was treated subcutaneously with 40 mg kg<sup>–1</sup> phenylmethylsulfonyl fluoride (PMSF), followed by 1000 mg kg<sup>–1</sup> TOCP 24 h later. Proteins in the brains of hens were separated by two‐dimensional polyacrylamide gel electrophoresis on day 5 after TOCP administration. Mass spectrometry identified eight differentially expressed proteins. Among these proteins, downregulated expression of glutamine synthetase (GS) in the brains of hens after TOCP treatment was further confirmed by real time RT‐PCR and ELISA. Moreover, the brains of hens exposed to TOCP exhibited increased levels of glutamate (Glu) and cytosolic calcium concentration ([Ca<sup>2+</sup>]<italic><sub>i</sub></italic>), and a decreased level of glutamine (Gln). However, there were no significant differences in GS expression or levels of Glu, Gln, and [Ca<sup>2+</sup>]<italic><sub>i</sub></italic> in the brains of hens among the groups on day 21 after TOCP administration. These results indicate that TOCP exposure downregulates GS expression in the brains of hens, and that downregulation of GS is accompanied by increased levels of Glu and [Ca<sup>2+</sup>]<italic><sub>i</sub></italic> in the early stage after TOCP administration. It is also suggested that the downregulated expression of GS might be associated with OPIDN through the disruption of homeostasis of the Glu–Gln cycle and [Ca<sup>2+</sup>]<italic><sub>i</sub></italic>. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p> </abstract> … (more)
- Is Part Of:
- Journal of applied toxicology. Volume 34:Issue 12(2014)
- Journal:
- Journal of applied toxicology
- Issue:
- Volume 34:Issue 12(2014)
- Issue Display:
- Volume 34, Issue 12 (2014)
- Year:
- 2014
- Volume:
- 34
- Issue:
- 12
- Issue Sort Value:
- 2014-0034-0012-0000
- Page Start:
- 1352
- Page End:
- 1360
- Publication Date:
- 2013-12-12
- Subjects:
- Toxicology -- Periodicals
Industrial toxicology -- Periodicals
Environmentally induced diseases -- Periodicals
Toxicology -- Periodicals
615.9005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-1263/issues ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jat.2965 ↗
- Languages:
- English
- ISSNs:
- 0260-437X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4947.130000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3312.xml