Literature DB >> 35263737

Endocannabinoid System in Polycystic Kidney Disease.

Jost Klawitter1, Cristina Sempio1, Matthew J Jackson1, Peter H Smith1, Katharina Hopp2, Michel Chonchol2, Berenice Y Gitomer2, Uwe Christians1, Jelena Klawitter1,2.   

Abstract

INTRODUCTION: Autosomal dominant polycystic kidney disease (ADPKD) is a commonly inherited disorder characterized by renal cyst formation. A major pathological feature of ADPKD is the development of interstitial inflammation. The endocannabinoid (EC) system is present in the kidney and has recently emerged as an important player in inflammation and the pathogenesis of progressive kidney disease.
METHODS: Data on ECs were collected using a validated mass spectrometry assay from a well-characterized cohort of 102 ADPKD patients (at baseline and after 2- and 4 years on standard vs. rigorous blood-pressure control) and compared to 100 healthy subjects.
RESULTS: Compared to healthy individuals, we found higher interleukins-6 and -1b as well as reduced plasma levels of anandamide (AEA), 2-arachidonoyl-glycerol (2-AG), and their congeners in ADPKD patients. Baseline AEA concentration negatively associated with the progression of ADPKD as expressed by the yearly percent change in height-corrected total kidney volume and positively with the yearly change in renal function (measured as estimated glomerular filtration rate, ΔeGFR). AEA analog palmitoylethanolamide (PEA) is also associated positively with the yearly change in eGFR. DISCUSSION AND
CONCLUSION: The results of the present study suggest that ADPKD patients present with lower levels of ECs and that reestablishing the normality of the renal EC system via augmentation of AEA, PEA, and 2-AG levels, either through the increase of their synthesis or through a reduction of their degradation, could be beneficial and may present a promising therapeutic target in said patients.
© 2022 S. Karger AG, Basel.

Entities:  

Keywords:  2-Arachidonoylglycerol; Anandamide; Autosomal dominant polycystic kidney disease; Endocannabinoids

Mesh:

Substances:

Year:  2022        PMID: 35263737      PMCID: PMC9173653          DOI: 10.1159/000522113

Source DB:  PubMed          Journal:  Am J Nephrol        ISSN: 0250-8095            Impact factor:   4.605


  60 in total

1.  Production and physiological actions of anandamide in the vasculature of the rat kidney.

Authors:  D G Deutsch; M S Goligorsky; P C Schmid; R J Krebsbach; H H Schmid; S K Das; S K Dey; G Arreaza; C Thorup; G Stefano; L C Moore
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Review 4.  Renal volume, renin-angiotensin-aldosterone system, hypertension, and left ventricular hypertrophy in patients with autosomal dominant polycystic kidney disease.

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Review 8.  Cannabinoid Receptor 1 Inhibition in Chronic Kidney Disease: A New Therapeutic Toolbox.

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9.  Experimental cannabinoid 2 receptor-mediated immune modulation in sepsis.

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10.  Macrophages promote polycystic kidney disease progression.

Authors:  Katherine I Swenson-Fields; Carolyn J Vivian; Sally M Salah; Jacqueline D Peda; Bradley M Davis; Nico van Rooijen; Darren P Wallace; Timothy A Fields
Journal:  Kidney Int       Date:  2013-02-20       Impact factor: 10.612

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