Elevated cannabinoid receptor 1 and G protein‐coupled receptor 55 expression in proximal tubule cells and whole kidney exposed to diabetic conditions. (March 2015)
- Record Type:
- Journal Article
- Title:
- Elevated cannabinoid receptor 1 and G protein‐coupled receptor 55 expression in proximal tubule cells and whole kidney exposed to diabetic conditions. (March 2015)
- Main Title:
- Elevated cannabinoid receptor 1 and G protein‐coupled receptor 55 expression in proximal tubule cells and whole kidney exposed to diabetic conditions
- Authors:
- Jenkin, Kayte A
McAinch, Andrew J
Zhang, Yuan
Kelly, Darren J
Hryciw, Deanne H - Abstract:
- <abstract abstract-type="main" id="cep12355-abs-0001"> <title>Summary</title> <p>Hyperglycaemia increases the risk of developing diabetic nephropathy, with primary targets in the glomerulus and proximal tubule. Importantly, glomerular damage in the kidney leads to elevated albumin levels in the filtrate, which contributes to tubular structural modifications that lead to dysfunction. Diabetes alters the endocannabinoid system in a number of target organs, with previous research characterizing tissue‐specific changes in the expression of the cannabinoid receptor 1 (CB<sub>1</sub>) and G protein‐coupled receptor 55 (GPR55), a putative cannabinoid receptor, in diabetes. Although these receptors have a functional role in the cannabinoid system in the kidney, there has been little investigation into changes in the expression of CB<sub>1</sub> and GPR55 in the proximal tubule under diabetic conditions. In this study, CB<sub>1</sub> and GPR55 messenger RNA and protein levels were quantified in cultured human kidney cells and then treated with either elevated glucose, elevated albumin, or a combination of glucose and albumin for 4, 6, 18, or 24 h. In addition, CB<sub>1</sub> and GPR55 protein expression was characterized in whole‐kidney lysate from streptozotocin‐induced diabetic Sprague‐Dawley rats. <italic>In vitro</italic> exposure to elevated glucose and albumin increased CB<sub>1</sub> and GPR55 messenger RNA and protein expression in proximal tubule cells in a time‐dependant<abstract abstract-type="main" id="cep12355-abs-0001"> <title>Summary</title> <p>Hyperglycaemia increases the risk of developing diabetic nephropathy, with primary targets in the glomerulus and proximal tubule. Importantly, glomerular damage in the kidney leads to elevated albumin levels in the filtrate, which contributes to tubular structural modifications that lead to dysfunction. Diabetes alters the endocannabinoid system in a number of target organs, with previous research characterizing tissue‐specific changes in the expression of the cannabinoid receptor 1 (CB<sub>1</sub>) and G protein‐coupled receptor 55 (GPR55), a putative cannabinoid receptor, in diabetes. Although these receptors have a functional role in the cannabinoid system in the kidney, there has been little investigation into changes in the expression of CB<sub>1</sub> and GPR55 in the proximal tubule under diabetic conditions. In this study, CB<sub>1</sub> and GPR55 messenger RNA and protein levels were quantified in cultured human kidney cells and then treated with either elevated glucose, elevated albumin, or a combination of glucose and albumin for 4, 6, 18, or 24 h. In addition, CB<sub>1</sub> and GPR55 protein expression was characterized in whole‐kidney lysate from streptozotocin‐induced diabetic Sprague‐Dawley rats. <italic>In vitro</italic> exposure to elevated glucose and albumin increased CB<sub>1</sub> and GPR55 messenger RNA and protein expression in proximal tubule cells in a time‐dependant manner. In whole kidney of streptozotocin‐induced diabetic rats, CB<sub>1</sub> protein was upregulated, whereas GPR55 protein concentration was not altered. Thus, expression of CB<sub>1</sub> and GPR55 in proximal tubules is altered in response to elevated levels of glucose and albumin. Further investigations should determine if these receptors are effective physiological targets for the treatment and prevention of diabetic nephropathy.</p> </abstract> … (more)
- Is Part Of:
- Clinical and experimental pharmacology and physiology. Volume 42:Number 3(2015:Mar.)
- Journal:
- Clinical and experimental pharmacology and physiology
- Issue:
- Volume 42:Number 3(2015:Mar.)
- Issue Display:
- Volume 42, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 42
- Issue:
- 3
- Issue Sort Value:
- 2015-0042-0003-0000
- Page Start:
- 256
- Page End:
- 262
- Publication Date:
- 2015-03
- Subjects:
- Clinical pharmacology -- Periodicals
Pharmacology, Experimental -- Periodicals
Physiology, Experimental -- Periodicals
Physiology, Pathological -- Periodicals
615.1 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=cep ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1440-1681.12355 ↗
- Languages:
- English
- ISSNs:
- 0305-1870
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.252000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3939.xml