ABH

ABH (400 μg/day; p.o.; once daily; 25 days) can reduce arginase activity in the penile tissue of aged rats, improve erectile function, and make erectile hemodynamic indicators close to the level of young rats^[4].
ABH (0.1 mM, 0.1 mL; topical application; once every 8 hours; 14 days) can significantly promote wound healing in mice^[5].
ABH (5 mg/kg; s.c.; once 1 hour before surgery; single administration) can increase plasma nitrite levels in rats with pneumoperitoneum, maintain nitric oxide synthase (NOS) activity, reduce oxidative stress and inflammatory response, and reduce the severity of lung injury^[6].
ABH (10 mg/kg; p.o., drinking water; once daily) can inhibit the increase of arginase activity and A1 expression in vascular endothelial cells of obese mice induced by a high-fat and high-sugar diet, reduce inflammation and pathological remodeling of visceral adipose tissue (VAT), including reducing inflammatory monocyte infiltration, macrophage polarization to M1 type, improving adipocyte size, fibrosis and capillary density^[7].
ABH (100 mg; i.p.; once at 24, 48, 60, 70 h after infection or continuously administered until day 3 after infection) can increase NO production in the lungs of mice infected with Pseudomonas aeruginosa, improve L-arginine availability, reduce L-ornithine concentration, and do not increase the levels of lung inflammatory markers^[8].
ABH (400 µg/kg/day; subcutaneous osmotic pump injection; once/day; 21 days) can reduce the mean arterial blood pressure and improve the vascular reactivity of the carotid and femoral arteries in a rat model of hypertension induced by chronic intermittent hypoxia (CIH)^[9].
ABH (10 mg/kg/day; drinking water administration; continuous administration; 6 months) can improve endothelial function, reduce aortic stiffness and fibrosis, and reduce plasma and aortic arginase activities in a mouse model of obesity-related type 2 diabetes induced by a high-fat and high-sugar diet^[10].
ABH (400 µg/day; subcutaneous osmotic pump administration; continuous administration) can preserve the total volume of the fetal lung, prevent excessive proliferation of pulmonary vascular smooth muscle cells, and improve the number of pulmonary vessels and lung morphology in a rat model of congenital diaphragmatic hernia (CDH) induced by Nitrofen (HY-B1877)^[11].