Abstract

The lipids of horse hoof have been analyzed by quantitative thin-layer chromatography. The major components include cholesterol (37-40%), six groups of ceramides (10-15%), and cholesteryl sulfate (15-20%). Free fatty acids are abundant (15.8%) in the outer fully keratinized hoof, but are present at only low levels (3.1%) in the softer hyponychium. The material identified as cholesteryl sulfate was isolated by preparative thin-layer chromatography and characterized by a combination of chemical, chromatographic, and spectroscopic methods. The infrared spectrum of the isolated material had absorption bands at 800, 1063, 1200, and 1235 cm-1, indicating a sulfate ester. This sulfolipid was nonsaponifiable, but upon acid hydrolysis yielded cholesterol as the only charrable product, which was identified by its chromatographic behavior and by its electron impact mass spectrum. The isolated sulfolipid also had the same mobility on thin-layer chromatography as authentic cholesteryl sulfate in several different solvent systems. Sulfated gangliosides, which were previously reported to be major horse hoof lipids, were not found among the principal lipid components in the present study. It is concluded that cholesteryl sulfate is the major polar lipid of horse hoof. This may be a significant factor determining the high degree of cohesiveness of this fully keratinized tissue.

Highlights

  • The lipids of horse hoof have been analyzed by quantitativethin-layer chromatography.The major components include cholesterol (37-40%), six groups of ceramides (1015%) and cholesteryl sulfate (1 5-20%)

  • This group of lipids consists of several unidentified minor components and one major spot that had the same thin-layer chromatography (TLC) mobility as authentic cholesteryl sulfate (Steraloids, Inc., Wilton, NH)

  • After hydrolysis with 1 N HCI in methanol containing 20 M water at 65°C for 18 hrs, only one charrable material was produced from each sample, and this had the same mobility on TLC as cholesterol

Read more

Summary

METHODS AND RESULTS

Fresh trimmings from horse hooves were obtained from a local farrier. T h e hoof material was rinsed under tap water to reduce surface contamination and dried thoroughly in vacuo. This group of lipids consists of several unidentified minor components and one major spot that had the same TLC mobility as authentic cholesteryl sulfate (Steraloids, Inc., Wilton, NH). Upon charring with sulfuric acid, both standard cholesteryl sulfate and the materials isolated from horse hoof and hyponychium produced a characteristic red-violet color prior to turning black. The materials from both the inner and outer hoof comigrated with authentic cholesteryl sulfate on silicic acid TLC in a variety of different neutral, acidic, and basic solvent systems having different polarities. The purified lipid was found to be unreactive during saponification with 1 N methanolic KOH at 60°C for cholesteryl sulfate ceramides 8 nonpolars

Rj for Hoof Lipid and Cholesteryl Sulfate
DISCUSSION
Cholesteryl sulfate
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call