Could cannabinoid pathways help kidneys recover from injury?

Emerging roles of cannabinoid pathways in renal injury and repair.

Frontiers in pharmacology • • Review • Highly Relevant
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AI Summary

Chronic kidney disease and acute kidney injury can damage the kidney’s filtering structures and may progress to severe loss of kidney function. This mechanistic review examines how cannabinoid signalling may influence these processes, focusing on the kidney’s CB1 and CB2 receptors as well as emerging targets such as GPR55, GPR18, and GPR119.

Evidence from animal models suggests that targeting cannabinoid-related pathways could help modulate kidney injury and repair, but the abstract does not report clinical trial results or quantitative treatment effects. The review also highlights interactions with other systems, including AT1, TRPV1, and PPARγ, pointing to potential therapeutic targets rather than established cannabis-based treatments. For cannabis users, this means the findings do not show that cannabis or over-the-counter cannabinoids prevent or treat kidney disease; they identify biological pathways that require further study.

💡 Key Findings

1
The kidney expresses CB1 and CB2 receptors, and cannabinoid signalling may influence kidney disease processes.
Good
70%
2
Animal-model evidence suggests that targeting cannabinoid receptors could modulate the progression of chronic and acute kidney injury.
Good
60%
3
Emerging cannabinoid-related receptors, including GPR55, GPR18, and GPR119, may represent potential therapeutic targets, but their roles remain insufficiently characterized.
Good
60%
4
The review identifies interactions between cannabinoid receptors and other pathways, including AT1, TRPV1, and PPARγ, as important open questions in kidney disease research.
Good
60%

📄 Original Abstract

Chronic kidney disease (CKD) is a significant health problem around the world. It can progress towards end-stage renal disease (ESRD), in which the current therapeutic options are dialysis and kidney transplant, which have several challenges in therapy compliance and finding a donor. There is a crosstalk between high blood pressure, diabetes, and obesity, which are the leading causes of CKD. The increased prevalence of these conditions, plus the ageing population, highlights the importance of finding new therapies to prevent and stop the progression of CKD. At the cellular level, CKD is characterized by the progressive loss of podocytes in the kidney glomeruli, reducing their filtration capacity. Other hallmarks of CKD are also part of acute kidney injury (AKI) pathogenesis, and both conditions are interlinked. The renal system expresses cannabinoid receptor types 1 and 2 (CB1 and CB2, respectively). There is evidence in animal models that targeting the cannabinoid receptors could modulate the progression of CKD and AKI. The role of cannabinoid signalling has not been sufficiently explored; several receptors that are not fully characterized have emerged as putative cannabinoid receptors (i.e., GPR55, GPR18, and GPR119), and some have been implicated in kidney pathophysiology. Moreover, cannabinoid receptors also interact and/or regulate other receptors (e.g., AT1, TRPV1, and PPARγ). Thus, there are several open questions regarding the role that cannabinoid signalling may play in the context of kidney diseases. In this mechanistic review, we examined the pharmacological actions of classic and emerging cannabinoid receptors on the renal system to identify potential therapeutic targets for kidney disease.

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