Cross-Talk between the (Endo)Cannabinoid and Renin-Angiotensin Systems: Basic Evidence and Potential Therapeutic Significance

This review is dedicated to the cross-talk between the (endo)cannabinoid and renin angiotensin systems (RAS). Activation of AT(1) receptors (AT(1)Rs) by angiotensin II (Ang II) can release endocannabinoids that, by acting at cannabinoid CB1 receptors (CB(1)Rs), modify the response to AT(1)R stimulation. CB1R blockade may enhance AT(1)R-mediated responses (mainly vasoconstrictor effects) or reduce them (mainly central nervous system-mediated effects). The final effects depend on whether stimulation of CB(1)Rs and AT(1)Rs induces opposite or the same effects. Second, CB1R blockade may diminish AT(1)R levels. Third, phytocannabinoids modulate angiotensin-converting enzyme-2. Additional studies are required to clarify (1) the existence of a cross-talk between the protective axis of the RAS (Ang II-AT(2) receptor system or angiotensin 1-7-Mas receptor system) with components of the endocannabinoid system, (2) the influence of Ang II on constituents of the endocannabinoid system and (3) the (patho)physiological significance of AT(1)R-CB1R heteromerization. As a therapeutic consequence, CB1R antagonists may influence effects elicited by the activation or blockade of the RAS; phytocannabinoids may be useful as adjuvant therapy against COVID-19; single drugs acting on the (endo)cannabinoid system (cannabidiol) and the RAS (telmisartan) may show pharmacokinetic interactions since they are substrates of the same metabolizing enzyme of the transport mechanism.

Automated summary

(English Summary:) This review explores the cross-talk between the (endo)cannabinoid and renin-angiotensin systems, focusing on the effects of CB1 receptor activation and blockade on AT(1) receptor-mediated responses. It also discusses the modulation of angiotensin-converting enzyme-2 by phytocannabinoids and the potential therapeutic implications of targeting both systems. Further research is needed to elucidate the interaction between the protective axis of the RAS and the endocannabinoid system, the influence of Ang II on endocannabinoid system components, and the physiological significance of AT(1)R-CB1R heteromerization.