Journal of Applied Physiology · 1992 · 57 citations · 0 references
MedicinePharmacologyCardiovascular PharmacotherapyPharmacodynamicsToxicodynamicsAcute Lung InjuryEndothelial DysfunctionHemodynamic PharmacologyVasodilator TherapyEndothelial Function ModulationHemodynamic Effects Of VasodilatorsPulmonary Vasodilator TherapyRelaxation ProcessesVascular Endothelial DysfunctionVasoactive Drug Administration
The effects of tumor necrosis factor (TNF) on hypoxic pulmonary vasoconstriction (HPV) and endothelium-dependent relaxation were examined in a blood-perfused rat lung preparation. Lungs from TNF-treated rats (0.26 mg/kg iv 12 h before experimentation) had a significantly greater HPV and a reduced vasorelaxant response to the endothelium-dependent vasodilator acetylcholine (ACh) but a similar vasorelaxant response to the endothelium-independent vasodilator nitroprusside compared with lungs from control rats (pretreated with 0.1 ml saline iv). Pentoxifylline (20 mg/kg iv and ip 20 min before administration of TNF) had no detectable effect on either HPV or ACh-induced relaxation but completely negated the augmentation on HPV and the inhibiting action on ACh-induced relaxation caused by TNF. The TNF effect on ACh relaxation was unaffected by pretreatment with L-arginine. These results indicate that TNF induces endothelial dysfunction and enhances HPV, effects that are inhibited by pentoxifylline.