Related Experiment Video
Updated: May 5, 2026

09:36
Recombinant α- β- and γ-Synucleins Stimulate Protein Phosphatase 2A Catalytic Subunit Activity in Cell Free Assays
Published on: August 13, 2017
8.1K
Pyridoxal phosphate as an antisickling agent in vitro
The Journal of Clinical Investigation
|May 1, 1983
Summary
Pyridoxal phosphate and pyridoxal inhibit sickle cell sickling in intact erythrocytes. Pyridoxal phosphate
Area of Science:
- Hematology
- Biochemistry
- Molecular Biology
Background:
- Pyridoxal phosphate inhibits purified hemoglobin S gelation.
- Antisickling activity in intact erythrocytes has not been previously demonstrated.
Purpose of the Study:
- To investigate the antisickling activity of pyridoxal phosphate and pyridoxal in intact erythrocytes.
- To compare their effects on hemoglobin modification, oxygen affinity, and sickling.
Main Methods:
- Washed erythrocytes were incubated with pyridoxal phosphate or pyridoxal.
- Hemoglobin modification, oxygen affinity, and sickling extent under hypoxia were measured.
Main Results:
- Pyridoxal phosphate modified hemoglobin slower than pyridoxal.
- Pyridoxal phosphate inhibited sickling significantly, largely independent of oxygen binding.
- Pyridoxal inhibited sickling, primarily dependent on increased oxygen binding.
Conclusions:
- Both pyridoxal phosphate and pyridoxal demonstrate antisickling activity in intact erythrocytes.
- They differ in modification kinetics, effects on oxygen affinity, and mechanism of action.
Related Concept Videos
Anticholinesterase Agents: Poisoning and Treatment
2.0K
Anticholinesterases, also known as cholinesterase inhibitors, work by blocking the breakdown of acetylcholine, leading to its accumulation in the synaptic cleft. This accumulation indirectly enhances both muscarinic and nicotinic actions. These agents are classified as reversible or irreversible based on their mechanism of action.
Irreversible agents form a strong bond with the cholinesterase enzyme, making it inactive. The breakdown of the phosphorylated enzyme is...
Irreversible agents form a strong bond with the cholinesterase enzyme, making it inactive. The breakdown of the phosphorylated enzyme is...
2.0K
Depolarizing Blockers: Pharmocokinetics
784
Depolarizing blockers are administered through intravenous injection. Succinylcholine is the most common choice of depolarizing blockers in emergency clinical practices. Although they have a rapid onset, they readily diffuse away from the motor end plate into the extracellular fluid. They are metabolized by enzymes such as liver butyrylcholinesterase and plasma pseudocholinesterases. This produces a short duration of action, typically 5-10 minutes long, unlike nondepolarizing blockers, which...
784

