In a third study published online by Science on 6 April (www.sciencexpress.org), molecular geneticist Valter Longo of the University of Southern California in Los Angeles and colleagues battered a population of yeast mutants with heat or paraquat, a chemical that
creates reactive oxygen molecules.
More research produced the answer: Vitamin C induced what is known as a Fenton reaction, causing iron to react with other molecules to
create reactive oxygen species that kill the TB bacteria.
In earlier versions, the nickel - molybdenum - zinc alloy catalyst used to produce the hydrogen also
created reactive oxygen species, which would attack and destroy the bacteria's DNA.
Not exact matches
The cause of the damage is still poorly understood, but radiation is known to
create highly
reactive oxygen - containing molecules in the body.
Sunlight and toxins do much of the damage, but the biggest culprit may be highly
reactive byproducts
created as cells use
oxygen to turn sugar into energy.
That light is absorbed by the chlorine - based molecules, which then excite nearby
oxygen molecules,
creating a highly
reactive form of
oxygen, known as singlet
oxygen, that rips apart nearby biomolecules and kills the tumor cell.
The damaged mitochondria become increasingly dysfunctional, producing even more
reactive oxygen species and
creating an undesirable cycle.
Physiologist Dino Giussani and colleagues at the University of Cambridge in the United Kingdom theorized that hypoxia promotes harm in the womb primarily through stress caused when the low level of
oxygen creates an overload of highly
reactive molecules known as free radicals.
I've been experimenting with T10 dextran coated iron oxide nanoparticles, obviously not the same as fullerenes, but still a very interesting tool, I've been testing if the coating is giving the particle antioxidant abilities because of it's the (basically) indigestable sugar chains (glucose)
creating a high surface area which are largely made from hydroxyl groups, I hypothesised this act's as a «sink» for
reactive oxygen species converting them to water.
The addition of this pendant catalyst
created an MnP - PVPON / TA capsule with the following characteristics: 1) the microcapsules synergistically remove
reactive oxygen species, including superoxide and hydrogen peroxide, at dramatically increased rates compared to unmodified TA / PVPON microcapsules; 2) the microcapsule does not degrade with long exposure to
reactive oxygen species; and 3) the microcapsules are nontoxic to mouse splenocytes.
It has been thoroughly researched and shown that the overall health of a body is intrinsically linked to the health of its cells and their ability to metabolize oxidation.5 When oxidative metabolism's limits are exceeded free radicals and
reactive oxygen species (ROS) are
created and start to build up within the body.
But 0.5 to 5 percent of the time,
reactive oxygen species (ROS) are
created.
This causes the body to
create unstable molecules known as
reactive oxygen species (ROS).
But the process of producing ATP
creates a huge burst of damaging free radicals known as
reactive oxygen species (ROS), which are the chief cause of mitochondria destruction.
The damage may cause mutations to the DNA, possibly
creating a GREATER NUMBER of
Reactive Oxygen Species.
When your body is able to burn fat for fuel, your liver
creates water - soluble fats called ketones that burn far more efficiently than carbs, thereby
creating fewer
reactive oxygen species (ROS) and secondary free radicals.
As congestive heart failure progresses, the formation of «free radicals» (
reactive molecules
created during
oxygen metabolism) increases heart cell damage.
Global warming is implicated in the loss of Arctic ozone because greenhouse gases trap energy lower down, heating up the atmosphere nearer the ground but cooling the stratosphere,
creating conditions conducive to the formation of the
reactive chemicals that break apart the three -
oxygen molecules of ozone.