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. 2022 Jun 6;23(11):6350. doi: 10.3390/ijms23116350

Table 3.

Examples of the cross-talk between the (endo)cannabinoid and angiotensin 1-7.

Species Model Basal Treatment (Concentration (μM) or Dose) Effect Intervention (Concentration (μM) or Dose) Influence on the Agonist Effect Final Conclusion of the Authors References
rats ovariectomized pseudopregnant steroid treatment and bolus of oil leading to
decidualization
uterus:
↓CB1Rs,
↑CB2Rs, ↔MAGL, ↓FAAH
Ang 1-7
(24 μg/kg/h; i.u. for 5 days)
uterus:
↑CB1Rs, ↑CB2Rs, ↑MAGL, ↔FAAH
Ang 1-7 augments the expression of CB1Rs, CB2Rs, and MAGL in the decidualized uterus and thus may interfere with early events of decidualization [92]
rats
SHR
WKY
conscious
(compounds microinjected into the PVN, doses in nmol/rat; if not stated otherwise)
Ang 1-7
(0.03)
or
CP55940
(0.1) +
AM251 3 μmol/kg i.v.
both treatments: ↑BP stronger in SHR than in WKY A-779 (3)
AM251 (30)
↓pressor effect of Ang 1-7 and CP55940
↓pressor effect of Ang 1-7
mutual interaction in the PVN between the CB1Rs and the receptors for Ang 1-7 responsible for stimulation of the pressor response [55]

↓—decrease; ↑—increase; ↔—no change; Ang 1-7, angiotensin 1-7; BP, blood pressure; CB1R, cannabinoid receptor type 1; CB2R, cannabinoid receptor type 2; FAAH, fatty acid amide hydrolase; i.u., intrauterine; i.v., intravenous; MAGL, monoacylglycerol lipase; PVN, paraventricular nucleus of the hypothalamus; SHR, spontaneously hypertensive rats; WKY, Wistar Kyoto rats.