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K Nakaoji

Publications and source records attributed to K Nakaoji.

4 recordsLinked to original sources

Bisbenzylisoquinoline alkaloids from Stephania cepharantha and their effects on proliferation of cultured cells from the murine hair apparatus.

Bisbenzylisoquinoline alkaloids were isolated from Stephania cepharantha Hayata and their proliferative activities on cultured hair cells from the murine skin were evaluated. Cepharanthine (1), cepharanoline (9), isotetrandrine (2), and berbamine (7) showed significant activities in the range of 0.01-0.1 microgram/ml, but had no activity on cultured keratinocytes or fibroblasts from the murine skin.

Alkaloids↗

Norreticuline and reticuline as possible new agents for hair growth acceleration.

(S)-Norreticuline and (S)-reticuline have been shown to stimulate the proliferation of cultured cells from the murine hair apparatus significantly. Furthermore, these activities were found on cultured hair cells, but not on cultured keratinocytes or fibroblasts from murine skin. In addition, (S)-norreticuline significantly stimulated mouse hair regrowth. These results suggest that (S)-norreticuline and (S)-reticuline could have specific activities on hair apparatus cells and might be useful as active compounds for accelerating hair growth.

Alkaloids↗

Further immunocytochemical characterization of cultured hair apparatus cells.

In immunocytochemical studies of cultured hair apparatus cells we employed anti-hair keratin monoclonal antibodies (HKN-2, HKN-4, HKN-5, HKN-6 and HKN-7) and compared the results with electron microscopic studies. On day 1, the cultured cells positively stained with HKN-2 (52%), HKN-4 (50%), HKN-5 (43%), HKN-6 (33%), or HKN-7 (37%). On day 3, more than 88% of the cells showed no reaction to any antibody. On day 6, most of the cells stained with all of the antibodies: HKN-2 (96%), HKN-4 (92%), HKN-5 (80%), HKN-6 (72%) and HKN-7 (74%). These reactivities were maintained until day 13. Electron microscopic studies revealed that, on day 1, half of the observed cells were immature and 47% of them were already differentiated. Most (88%) of the cells showed immature features and the percentage of differentiated cells had decreased by day 3. The differentiated cells (87%) reappeared by day 6, and degenerated cells (63%) increased by day 13. These immunocytochemical results were consistent with those of simultaneous electron microscopic studies, demonstrating that immature cells proliferated and differentiated into subpopulations of each hair apparatus layer type, including the outer root sheath cells, in this culture system.

Animals↗