1993
DOI: 10.3109/10520299309105637
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A Method for Determining the Activity State of Hair Follicles

Abstract: A histological method is described for determining the proportion of growing hair follicles in skin samples. A variation of the Sacpic staining method, modified for bulk processing, produces high contrast staining of the principal tissue types present in skin. In particular, the inner root sheath is accentuated, facilitating detection of active follicles. Skin preparations from a range of species are used to illustrate structural characteristics of follicles viewed in cross section at various stages of the hai… Show more

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Cited by 77 publications
(58 citation statements)
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“…All skin samples were fixed in 10% buffered formalin and processed by dehydration in increasing concentrations of ethanol and D-limonene (Histosolve; HD Scientific, Wetheril Park, New South Wales, Australia). Explants were embedded in paraffin wax in transverse orientation, and 7 mm serial sections were cut and stained using a modified SACPIC staining protocol (Nixon, 1993).…”
Section: Methodsmentioning
confidence: 99%
“…All skin samples were fixed in 10% buffered formalin and processed by dehydration in increasing concentrations of ethanol and D-limonene (Histosolve; HD Scientific, Wetheril Park, New South Wales, Australia). Explants were embedded in paraffin wax in transverse orientation, and 7 mm serial sections were cut and stained using a modified SACPIC staining protocol (Nixon, 1993).…”
Section: Methodsmentioning
confidence: 99%
“…Transverse sections of 7 mm were cut with a rotary microtome and stained by using the Sacpic staining procedure, modified by Nixon (1993). This dyeing method reveals the follicular inner root sheath (IRS, which shows activities only in the anagen phase) and the cellular layer of the outer root sheath, which are the main histological structures for defining skin follicular activity.…”
Section: Methodsmentioning
confidence: 99%
“…Skin samples were fixed (10% buffered formalin; weight/volume), processed through graded alcohols, and embedded, epidermal surface uppermost, in paraffin wax. The skin was then serially sectioned (8 |Lim) in the transverse plane and stained with adapted Sacpic stain (Nixon, 1993). Primary and secondary follicle activities were assessed according to staining characteristics of the inner-root sheath (Nixon, 1993).…”
Section: Methodsmentioning
confidence: 99%