Publications by authors named "L D Asico"

The kidney and brain play critical roles in the regulation of blood pressure. Neuropeptide FF (NPFF), originally isolated from the bovine brain, has been suggested to contribute to the pathogenesis of hypertension. However, the roles of NPFF and its receptors, NPFF-R1 and NPFF-R2, in the regulation of blood pressure, via the kidney, are not known.

View Article and Find Full Text PDF

Background: The thiazide-sensitive sodium chloride cotransporter (NCC) is the major apical sodium transporter located in the mammalian renal distal convoluted tubule (DCT). The amount of sodium reabsorbed in the DCT through NCC plays an important role in the regulation of extracellular fluid volume and blood pressure. Dopamine and its receptors constitute a renal antihypertensive system in mammals.

View Article and Find Full Text PDF

Reactive oxygen species are highly reactive molecules generated in different subcellular compartments. Both the dopamine D5 receptor (DR) and endoplasmic reticulum (ER)-resident peroxiredoxin-4 (PRDX4) play protective roles against oxidative stress. This study is aimed at investigating the interaction between PRDX4 and DR in regulating oxidative stress in the kidney.

View Article and Find Full Text PDF
Article Synopsis
  • HIV-associated nephropathy (HIVAN) affects kidney function, particularly damaging glomeruli and tubules, leading to sodium wasting in HIV/AIDS patients.
  • Research using Vpr-transgenic mice revealed that the HIV viral protein Vpr increases urinary sodium excretion while decreasing the expression of the Na+-Cl- cotransporter (NCC) in the kidneys.
  • Vpr also impairs the mineralocorticoid receptor (MR) activity needed for NCC regulation, indicating that it plays a key role in the mechanism behind sodium wasting in HIV-infected individuals.
View Article and Find Full Text PDF

The understanding of how biological membranes are organized and how they function has constantly been evolving over the past decades. Instead of just serving as a medium in which specific proteins are located, certain parts of the lipid bilayer contribute to platforms that assemble signaling complexes by providing a microenvironment that facilitates effective protein-protein interactions. G protein-coupled receptors (GPCRs) and relevant signaling molecules, including the heterotrimeric G proteins, key enzymes such as kinases and phosphatases, trafficking proteins, and secondary messengers, preferentially partition to these highly organized cell membrane microdomains, called lipid rafts.

View Article and Find Full Text PDF