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. Author manuscript; available in PMC: 2021 Mar 1.
Published in final edited form as: J Mol Cell Cardiol. 2020 Feb 11;140:1–9. doi: 10.1016/j.yjmcc.2020.02.004

Table 3.

Purinergic receptor-mediated vascular function in kidney.

Organ Species Diabetic model Nucleot(s)ide/stimuli Purinergic receptor Vascular effect Reference
Kidney Rat STZ ADO/renal occlusion A1R RBF↓ [39]
The A2BR antagonist A2BR Glomerulopathy and fibrosis↓ [47,48]
The A2AR agonist A2AR Glomerular inflammation and injury↓ [45,46]
The P2X7R agonist P2X7R Cortical blood flow↑, GFR↓ [36]
Rat GK Up4A P2R vascular contraction↑ [51]
Mouse Ins2+/−/A1AR−/− mutants A1R GFR↑, Glomerular Injury↑ [43]
Mouse alloxan-induced A1AR−/− A1R Glomerular Injury - [44]
Mouse STZ The A2BR agonist Endothelial A2BR Glomerular Injury↓ [49]
Mouse STZ with CD73−/− Adenosine Glomerular Injury↑ [49]
Mouse STZ with CD39−/− ATP/UTP Glomerular inflammation↑ [50]
Mouse HFD The P2X7R agonist P2X7R Renal inflammation and injury↑ [54]
P2X7R−/− Renal inflammation and injury↓

ADO: adenosine; CD39: ectonucleoside triphosphate diphosphohydrolase; CD73: ecto-5′-nucleotidase; GFR: glomerular filtration rate; GK: Goto Kakizaki; HFD: high fat diet; Ins2: also known as Akita+/−, a naturally occurring diabetic model; RBF: renal blood flow; STZ: streptozotocin; Up4A: uridine adenosine tetraphosphate; ↑: increased effect; ↓: decreased effect; −: no effect vs. control group.