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K S Leon

Publications and source records attributed to K S Leon.

2 recordsLinked to original sources

Peripheral nerve phospholipid composition: development in normal nerve and age-dependent changes in Wallerian degenerated nerve.

The phospholipid composition of normal peripheral nerve as a function of developmental age as well as that of Wallerian-degenerated nerve as a function of age at nerve transection and duration of Wallerian degeneration have been quantitated in rabbit sciatic nerve. During development, increases in the proportions of ethanolamine plasmalogen, sphingomyelin, and combined phosphatidyl serine plus phosphatidyl inositol and decreases in the proportions of phosphatidyl choline and phosphatidyl ethanolamine correlated well with the concurrent myelin accretion. During Wallerian degeneration, age-dependent changes in phospholipid composition were observed. The large and statistically significant increase in the proportion of phosphatidyl choline and decrease in the proportion of ethanolamine plasmalogen were manifest promptly in nerves transected at 2 weeks of age but in a delayed manner in nerves transected at 8, 12, and 20 weeks of age. The rate of loss of individual phospholipids was greater in nerves transected at younger ages. The findings from normal developing peripheral nerve may well serve as baseline data for subsequent studies of phospholipid composition in pathological peripheral nerve. The findings from Wallerian-degenerated peripheral nerve provide additional evidence for age-dependent chemical changes occurring in Wallerian-degenerated peripheral nerve that may be of significance in explaining the superior functional recovery from peripheral nerve injury observed in younger compared with older subjects.

Aging↗

A comparative-evolutionary study of lipids in the aging brain of mice.

The lipids of aging brain were studied using a comparative-evolutionary model involving two species of mice, Mus Musculus (Mus) and Peromyscus leucopus (Peromyscus). Mus ages 2.5 times faster than does Peromyscus. Brain weight, water content, cholesterol, and ethanolamine plasmalogen decreased and phosphatidyl ethanolamine increased in both species with age. Differences between species included 12% more cholesterol/g total lipid extract in Peromyscus than in Mus throughout life, a linear increase with age in lipid phosphorus/g fresh weight at a faster rate in Peromyscus over Mus, and a linear increase in the total lipid extract weight throughout life in Mus but a decrease in Peromyscus. Cerebroside, sulfatide and GM1 ganglioside all increased during maturation and then decreased in old age in both mice. Lipid-bound sialic acid (ganglioside) increased linearly throughout life in Peromyscus but decreased slightly in Mus. These changes are interpreted to mean that the cellular membranes of Peromyscus may be inherently more stable than those of Mus, Peromyscus is better able to preserve its neuronal cell population with age than is Mus, proliferation of non-myelin membranes may occur in both species in advanced age, and both species of mice may experience some loss of myelin with age.

Aging↗