Commentary: mannitol: molecule magnifique or a case of radical misinterpretation?

C E Gillbe1, F J Sage, J M Gutteridge

  • 1Department of Anaesthesia & Adult Intensive Care, Royal Brompton Hospital, London, UK.

Free Radical Research
|January 1, 1996
PubMed

Insights

Oxidative stress occurs when reactive oxygen species (ROS) overwhelm the body's defenses, causing molecular damage. Current therapeutic strategies, like using mannitol, show limited success in preventing this cellular damage from highly reactive ROS.

Area of Science:

  • Biochemistry
  • Cell Biology
  • Toxicology

Background:

  • Reactive oxygen species (ROS) are natural byproducts of biological processes.
  • An imbalance between ROS production and antioxidant capacity leads to oxidative stress.
  • Oxidative stress can cause significant damage to vital cellular molecules.

Purpose of the Study:

  • To investigate the role of hydroxyl radicals in cellular damage.
  • To evaluate the potential of mannitol as a therapeutic agent against ROS-induced damage.

Main Methods:

  • Analysis of ROS formation in biological systems.
  • Assessment of molecular damage under oxidative stress conditions.
  • Evaluation of mannitol's efficacy in mitigating ROS effects.

Main Results:

  • Hydroxyl radicals identified as the most potent ROS, causing rapid molecular damage.
  • Mannitol demonstrated limited effectiveness in preventing ROS-mediated cellular damage at therapeutic doses.

Conclusions:

  • The high reactivity of hydroxyl radicals poses a significant challenge for therapeutic intervention.
  • Current therapeutic approaches using mannitol are unlikely to prevent ROS-induced cellular damage effectively.

Related Concept Videos

Molecular Models02:00

Molecular Models

Physical models representing molecular architectures of chemical compounds play essential roles in understanding chemistry. The use of molecular models makes it easier to visualize the structures and shapes of atoms and molecules.
Qualitative Analysis03:46

Qualitative Analysis

For solutions containing mixtures of different cations, the identity of each cation can be determined by qualitative analysis. This technique involves a series of selective precipitations with different chemical reagents, each reaction producing a characteristic precipitate for a specific group of cations. Metal ions within a group are further separated by varying the pH, heating the mixture to redissolve a precipitate, or adding other reagents to form complex ions.
For instance, group IV...
Radical Halogenation: Stereochemistry01:33

Radical Halogenation: Stereochemistry

Stereochemistry is the study of the different spatial arrangements of atoms in a given molecule. The stereochemistry of radical halogenations can be understood from three different situations:
Halogenation to form a new chiral center:
Radical Anti-Markovnikov Addition to Alkenes: Overview01:25

Radical Anti-Markovnikov Addition to Alkenes: Overview

The addition of hydrogen bromide to alkenes in the presence of hydroperoxides or peroxides proceeds via an anti-Markovnikov pathway and yields alkyl bromides.
Radical Anti-Markovnikov Addition to Alkenes: Mechanism01:17

Radical Anti-Markovnikov Addition to Alkenes: Mechanism

The reaction of hydrogen bromide with alkenes in the presence of hydroperoxides or peroxides proceeds via anti-Markovnikov addition. The radical chain reaction comprises initiation, propagation, and termination steps.
The mechanism starts with chain initiation, which involves two steps. In the first chain initiation step, a weak peroxide bond is homolytically cleaved upon mild heating to form two alkoxy radicals. In the second initiation step, a hydrogen atom is abstracted by the alkoxy radical...
π Molecular Orbitals of the Allyl Radical01:27

π Molecular Orbitals of the Allyl Radical

Allyl radicals are three-carbon conjugated systems. They are readily formed as intermediates in halogenation reactions of alkenes involving the addition of halogen to the allylic carbon instead of the double bond. As seen in allyl cations and anions, each of the three sp2-hybridized carbon atoms in allyl radicals has an unhybridized p orbital. These orbitals combine to give three π molecular orbitals.
The allyl systems have identical molecular orbitals but differ in the number of π electrons.