Related Experiment Video
Updated: Feb 5, 2026

11:28
Analytical Techniques for Assaying Nitric Oxide Bioactivity
Published on: June 18, 2012
18.5K
[INVOLVEMENT OF NITRIC OXIDE CYNTHASE IN THE EARLY PHASE OF THE HEART ISCHEMIC PRECONDITIONING]
Rossiiskii Fiziologicheskii Zhurnal Imeni I.M. Sechenova
|September 8, 2018
Summary
Nitric oxide (NO) and NO-synthase (NOS) play a role in the cardioprotection during early ischemic preconditioning (IP). This review examines evidence supporting and refuting NOS involvement in IP
Area of Science:
- Cardiovascular Physiology
- Molecular Cardiology
- Biochemistry
Background:
- Ischemic preconditioning (IP) offers cardioprotection against ischemia-reperfusion injury.
- The precise role of nitric oxide (NO) and NO-synthase (NOS) in early IP remains debated.
Purpose of the Study:
- To review and analyze experimental evidence regarding the involvement of NO and NOS in the cardioprotective effects of early IP.
- To elucidate the mechanisms through which NO and NOS may mediate cardioprotection during IP.
Main Methods:
- Literature review of experimental studies on ischemic preconditioning and nitric oxide pathways.
- Analysis of data on nitrates, nitrites, NOS gene expression, and the effects of NOS blockers and NO donors.
Main Results:
- Evidence suggests NOS involvement in IP-induced cardioprotection, with increased nitrates/nitrites and NOS gene expression post-IP.
- Inhibition of NOS blocks IP's protective effect, while NO donors mimic IP's effects.
- Conflicting data also exists, highlighting the complexity of NOS involvement.
Conclusions:
- Nitric oxide and NO-synthase are likely involved in the early phase of ischemic preconditioning.
- Further research is needed to fully understand the intricate mechanisms of NO/NOS in IP-mediated cardioprotection.
More Related Videos
Related Concept Videos
Nitric Oxide Signaling Pathway
6.3K
Nitric oxide (NO), an inorganic gas, acts as a potent second messenger in most animal and plant tissues. NO diffuses out of the cells that produce it and enters the neighboring cells to generate a downstream response. NO synthase (NOS) catalyzes NO production by the deamination of the amino acid arginine. There are three isoforms of NOS. Endothelial cells have endothelial NOS (eNOS), nerve and muscle cells have neuronal NOS (nNOS), and macrophages produce inducible NOS (iNOS) upon exposure...
6.3K
Ischemic Heart Disease: Overview
3.4K
Ischemic heart disease occurs when the heart's blood supply dwindles, causing an ominous lack of oxygen and nutrients. This deficiency, stemming from reduced or obstructed blood flow, spells danger, leading to heart muscle damage and dysfunction.
Atherosclerosis, the primary malefactor, orchestrates this dangerous condition. It manifests as the accumulation of fatty deposits, akin to insidious plaques, within arterial walls. As time elapses, these plaques metamorphose, hardening and...
Atherosclerosis, the primary malefactor, orchestrates this dangerous condition. It manifests as the accumulation of fatty deposits, akin to insidious plaques, within arterial walls. As time elapses, these plaques metamorphose, hardening and...
3.4K
Phase I Oxidative Reactions: Overview
786
Phase I biotransformation, or functionalization, is a crucial chemical process that converts drugs and other xenobiotics into more water-soluble forms, facilitating expulsion from the body. It involves oxidative, reductive, and hydrolytic reactions that add or unveil polar functional groups on lipophilic substrates. Key players in phase I reactions are the mixed-function oxidases. Situated in liver cell microsomes, these enzymes predominantly carry out drug metabolism. They require molecular...
786
Oxidation Numbers
42.8K
In redox reactions, the transfer of electrons occurs between reacting species. Electron transfer is described by a hypothetical number called the oxidation number (or oxidation state). It represents the effective charge of an atom or element, which is assigned using a set of rules.
42.8K
Phase I Reactions: Oxidation of Carbon-Heteroatom and Miscellaneous Systems
421
Oxidative reactions are pivotal in metabolizing numerous compounds, including pharmaceutical drugs. These reactions often occur in carbon-heteroatom systems, such as carbon-nitrogen, carbon-sulfur, and carbon-oxygen.
In carbon-nitrogen systems, aliphatic and aromatic amines can undergo oxidative reactions. Secondary and tertiary amines, like those found in tricyclic antidepressants, can undergo N-dealkylation, a process that involves the oxidation of the alkyl group. In addition, oxidative...
In carbon-nitrogen systems, aliphatic and aromatic amines can undergo oxidative reactions. Secondary and tertiary amines, like those found in tricyclic antidepressants, can undergo N-dealkylation, a process that involves the oxidation of the alkyl group. In addition, oxidative...
421
Phase I Reactions: Oxidation of Aliphatic and Aromatic Carbon-Containing Systems
736
Phase I biotransformation reactions are integral to drug metabolism, predominantly involving oxidative, reductive, and hydrolytic transformations. Chief among these are oxidative reactions, which enhance the hydrophilicity of xenobiotics and introduce polar functional groups to facilitate their elimination from the body.
Oxidation reactions are fundamental in aromatic carbon-containing systems. An example is the hydroxylation of phenobarbital, a process that transforms it into...
Oxidation reactions are fundamental in aromatic carbon-containing systems. An example is the hydroxylation of phenobarbital, a process that transforms it into...
736

