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. 2016 Jul 20;17(7):1098. doi: 10.3390/ijms17071098

Table 1.

Bilogical effects of Angiotensin A.

Angiotensin A References
Human embryonic kidney cells HEK-293 No difference in AT1 affinity to Ang A and Ang II ↑ affinity of AT2 for Ang A than for Ang II [17]
Vascular smooth-muscle cells Dose-dependent ↑ in cytosolic calcium inhibited by AT1 antagonist EXP-3174 [17]
proliferative effect Ang A > to Ang II [20]
Abdominal aorta New Zealand White rabbits Vasoconstriction ↓ in vessels from animals fed with atherogenic diet [19]
Isolated perfused kidney Dose-dependent vasoconstriction 90% of the maximal effect of Ang II inhibited by AT1 antagonist EXP-3174 no effect of AT2 antagonist PD123319 [17]
Normotensive rats intrarenal administration ↓ renal blood flow and ↑ renal vascular resistance ↓ effect of Ang A compared to Ang II improved by candesartan [18]
Normotensive rats i.v. administration ↑ BP ↓ by AT1-receptor blocker losartan no effect of AT2-antagonist PD123319 [20]
Spontaneously hypertensive rats i.v. administration ↑ BP both SHR and controls ↓ by AT1-receptor blocker candesartan no effect of AT2-antagonist PD123319 dose-dependent ↓ renal blood flow and ↑ renal vascular resistance in both SHR and controls ↓ effect of Ang A compared to Ang II no vasodilator response to Ang A or Ang II stimulation improved by candesartan no effect of AT2-antagonist PD123319 [18]
AT1-knockout mice ↑ BP in wild-type mice at ≈10× ↑ concentrations than Ang II no effect on BP in AT1A-knockout mice [17]
↑ BP and cortical vascular resistance and ↓ cortical blood flow in wild-type mice by Ang A and Ang II abolished in AT1A-knockout mice [18]
AT2-knockout mice ↑ cortical vascular resistance and ↓ cortical blood flow inhibited by candesartan no effect of AT2-antagonist PD123319 [18]