Skip to main content
. Author manuscript; available in PMC: 2021 Jun 1.
Published in final edited form as: Paediatr Drugs. 2020 Jun;22(3):279–293. doi: 10.1007/s40272-020-00384-5

Table 1.

Summary of different pre-clinical studies with arginine/citrulline supplementation

Disease Animal model The outcome of L-arginine or citrulline
   supplementation
Atherosclerosis Hypercholesterolemic rabbit - ↓ lesion surface area[110, 34, 38, 35]
- ↓intima thickness[34-36, 45]
- Absence of adherent monocytes or tissue macrophages[45]
- Prevents xanthoma formation[110]
LDL receptor knockout mouse
Vascular endothelial function Hypercholesterolemic rabbit - ↑ Endothelial dependent relaxation [34-39]
- ↑NO production/superoxide radical release[34, 39, 38, 111]
Pulmonary hypertension Hypoxia-induced pulmonary hypertension (rat and newborn pig)
Monocrotaline-induced pulmonary hypertension [43]
- ↑NO production [40, 42, 44, 53]
- ↓Pulmonary vascular resistance[40-44]
Systemic hypertension Salt-sensitive hypertensive (rats)
Spontaneous hypertension (young rat)

-↑NO production[48, 47]
Preeclampsia Insulin induced hypertension (pregnant rat) - ↓Blood pressure[49, 51, 50, 52]
- ↓urinary metabolites or nitrate[49, 51, 50, 52]
- ↓urine protein excretion[51, 52]
Adriamycin-induced nephropathy (pregnant rat)

↓=decrease; ↑= increase; LDL= Low Density Lipoprotein; NO= Nitric Oxide; PAH=Pulmonary Arterial Hypertension