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MYELINATION IN RAT BRAIN: METHOD OF MYELIN ISOLATION<sup>1</sup>
1.4K
Citations
28
References
1973
Year
Brain DevelopmentPeripheral NervesCellular NeurobiologyCellular PhysiologyMyelin YieldSocial SciencesNeuroregenerationExperimental NeuropathologyMyelin FractionsNeurologyNeuropathologyNeurological FunctionNeurochemistryMyelin CompositionSodium HomeostasisNervous SystemNeurological AssessmentNeurophysiologyNeuroanatomyCellular NeurosciencePhysiologyNutritional NeuroscienceNeuroscienceBrain ElectrophysiologyCentral Nervous SystemMedicine
A reliable method for isolating myelin from rat brain across developmental stages is essential for studying myelin composition. The study describes a procedure that yields myelin of consistent purity at all ages. The method eliminates microsomal contamination by maintaining a constant brain‑to‑volume ratio in the initial density gradient and incorporating two osmotic shocks and two low‑speed centrifugation steps. Using this protocol, myelin from 15‑day to 14‑month rats exhibited ATPase activities of 0.3–2.0 µmol Pi h⁻¹ mg⁻¹, Na⁺/K⁺‑ATPase activities of 0.1–1.6 µmol Pi h⁻¹ mg⁻¹, nucleic acid content of 0.2–0.7 % and ganglioside NANA of 0.04–0.07 %, with the highest constituent levels in 20‑day animals and increasing nucleic acid and ganglioside recovery with age and yield.
Abstract— A procedure is described for the preparation from rat brain of myelin having the same degree of purity at all ages. Such a procedure is essential for the study of myelin composition during development. Microsomal contamination was successfully eliminated by adjusting the method to maintain a constant amount of brain per unit volume in the initial density gradient step, and by including two osmotic shocks and two low‐speed centrifugation steps. Myelin prepared in this way from animals ranging from 15 days to 14months of age had a total ATPase activity of 0.3‐2.0 μmol of P i .h −1 .mg −1 dry wt of myelin, representing 0.1‐1.2 per cent recovery of the total homogenate activity; a Na + , K + ‐ ATPase activity of 0.1‐1.6 μfnol of P i .h −1 .mg −1 dry wt, representing 0.04‐1.5 per cent recovery; a nucleic acid content of 0.2‐0.7 per cent of myelin dry wt, representing 0.2‐2.0 per cent recovery; and a ganglioside NANA content of 0.04‐0.07 per cent of myelin dry wt. representing 0.2‐4.6 per cent recovery. The myelin prepared from 20‐day animals had the highest content of the first three constituents; otherwise the values of the four constituents were relatively constant per unit weight of myelin. The amounts of nucleic acid and ganglioside recovered in the myelin fractions increased with increasing age and myelin yield.
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