Histologic localization of serum constituents, Ca-45(2+), Cl-36(-), [C-14]urea, and [S-35]cysteine in forming hair after systemic administration

Citation
Pr. Stout et Ja. Ruth, Histologic localization of serum constituents, Ca-45(2+), Cl-36(-), [C-14]urea, and [S-35]cysteine in forming hair after systemic administration, DRUG META D, 28(2), 2000, pp. 113-117
Citations number
18
Categorie Soggetti
Pharmacology & Toxicology
Journal title
DRUG METABOLISM AND DISPOSITION
ISSN journal
00909556 → ACNP
Volume
28
Issue
2
Year of publication
2000
Pages
113 - 117
Database
ISI
SICI code
0090-9556(200002)28:2<113:HLOSCC>2.0.ZU;2-W
Abstract
To further investigate the chemical mechanisms involved in the accumulation of drugs or other compounds in hair, we characterized histologically the d eposition of radiolabeled serum constituents in the hair of BALB/c (albino) and C57 (pigmented) mice. The extent and location of the incorporation of a normal serum cation (Ca-45(2+)), a serum anion (Cl-36(-)), a neutral cons tituent ([C-14]urea), and a structural component of hair ([S-35]cysteine) w ere studied to provide a comparative framework for the examination of drugs deposited in hair from serum. Two mouse strains were used to evaluate the effect of hair pigmentation on deposition. Localization of deposition was o bserved using microautoradiography of skin sections from animals given a sy stemic dose of each tracer. The cation, Ca-45(2+), associated with melanocy tes and melanosomes of forming C57 hair within 5 min of dosing, but did not associate with the cells of forming BALB/c hair. This was consistent with previous results that indicated greater concentrations of Ca2+ in mature C5 7 mouse hair when compared with mature BALB/c hair. Both [C-14]urea and [S- 35]cysteine associated with all cells in the papilla of the forming hair of both C57 and BALB/c mice. This again was consistent with previous results that indicated that similar concentrations of cysteine and urea were incorp orated into mature C57 and BALB/c hair. The anion, Cl-36(-), did not associ ate with either C57 or BALB/c hair. The lack of deposition of Cl-36(-) may be due to the loss of the tracer during sample processing and suggests that Cl- could be removed from mature hair. These data confirm previous results that suggested that the melanin component of hair was capable of ionic int eractions and that the protein component was capable of neutral, lipophilic interactions. Our findings suggest a multicompartmental model of drug depo sition in hair.