scispace - formally typeset
J

Jeannette E. Doeller

Researcher at University of Alabama at Birmingham

Publications -  24
Citations -  3096

Jeannette E. Doeller is an academic researcher from University of Alabama at Birmingham. The author has contributed to research in topics: Sulfide & Geukensia demissa. The author has an hindex of 16, co-authored 24 publications receiving 2834 citations.

Papers
More filters
Journal ArticleDOI

Hydrogen sulfide attenuates myocardial ischemia-reperfusion injury by preservation of mitochondrial function

TL;DR: It is demonstrated that the delivery of H2S at the time of reperfusion limits infarct size and preserves left ventricular (LV) function in an in vivo model of myocardial ischemia-reperfusion (MI-R) and that either administration of H 2S or the modulation of endogenous production may be of clinical benefit in ischemic disorders.
Journal ArticleDOI

Hydrogen sulfide mediates the vasoactivity of garlic

TL;DR: It is shown that human RBCs convert garlic-derived organic polysulfides into hydrogen sulfide (H2S), an endogenous cardioprotective vascular cell signaling molecule, strongly supporting the hypothesis that H2S mediates the vasoactivity of garlic.
Journal ArticleDOI

Polarographic measurement of hydrogen sulfide production and consumption by mammalian tissues.

TL;DR: The use of a novel polarographic H2S sensor (PHSS) to follow rapid changes in H2s concentration in common buffered biological solutions with a detection limit near 10 nM is demonstrated and suggests the existence of dynamic steady-state cellular H 2S levels.
Journal ArticleDOI

High fat diet induces dysregulation of hepatic oxygen gradients and mitochondrial function in vivo.

TL;DR: It is hypothesized that mitochondrial defects induced by exposure to a HFD (high fat diet) contribute to a hypoxic state in liver and this is associated with increased protein modification by RNS (reactive nitrogen species).
Journal ArticleDOI

Hydrogen sulfide mediates vasoactivity in an O2-dependent manner.

TL;DR: In rat aorta, H( 2)S concentrations that mediate rapid contraction at high O(2) levels cause rapid relaxation at lower physiological O(1) levels, suggesting that it may be a putative vasoactive oxidation product that mediates constriction that modulates vascular tone in vivo.