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Biomedical subjects

G B Caughman

Publications and source records attributed to G B Caughman.

43 records · Page 3Linked to original sources

A postulated mechanism for heparin's potentiation of C1 inhibitor function.

Conflicting reports exist in the literature concerning the primary mechanism for heparin's inhibition of C1 hemolytic function. We provide evidence here that heparin's most effective inhibition is mediated through interaction with and potentiation of C1-INH. The molecular nature of the interaction between heparin and the C1-INH molecule is evidenced by an anodal shift in the electrophoretic mobility of C1-INH upon the addition of heparin.l We also demonstrate that C3 and C4 conversions in normal human serum by classical pathway activators such as heat-aggregated IgG are inhibited by addition of heparin, yet heparin does not prevent similar C3 conversion in serum depleted of C1-INH Heparin's inhibitory action is restored to C1-INH-depleted serum by the addition of purified C1-INH.

Complement Activation↗

Chemopreventive effects of green tea polyphenols correlate with reversible induction of p57 expression.

Green tea polyphenols are known to induce apoptosis in certain types of tumor cells. However, the mechanism(s) that enables normal cells to evade the apoptotic effect is still not understood. In this study, Western blot analysis combined with cycloheximide treatment was used to examine the effects of green tea polyphenols on the expression levels of p57, a cyclin-dependent kinase and apoptosis inhibitor, in normal human keratinocytes and in the oral carcinoma cell lines SCC25 and OSC2. The results showed that the most potent green tea polyphenol, (-)-epigallocatechin-3-gallate (EGCG), induced p57 in normal keratinocytes in a dosage- and time-dependent manner, while the levels of p57 protein in oral carcinoma cells were unaltered. The differential response in p57 induction was consistent with the apoptosis status detected by annexin V assay. The data suggest that the chemopreventive effects of green tea polyphenols may involve p57-mediated cell cycle regulation in normal epithelial cells.

Aged↗

Effects of denture base resins on oral epithelial cells.

The current proliferation of light-polymerized denture base resins and the continual modification of their formulations make standardized biocompatibility testing a necessity. The biocompatibilities of three light-polymerized denture base resins were compared using an in vitro epithelial cell culture system. The effect of varied lengths of polymerization of denture base resin on cell toxicity was examined. This study indicated that light-polymerized denture base resins have an effect on oral epithelial cells that appears to be related to the specific formulation of the material and not to the type of polymerization required. Varying the polymerization time or light-polymerization unit appeared to have little effect.

Acrylic Resins↗

Biocompatibility of visible light-polymerized denture base resins.

The biocompatibility of three commercial formulations of visible light-polymerized denture base resins was studied to determine its effects on the RNA and DNA synthesis of oral epithelial cells in vitro. Isotope incorporation into RNA or DNA was measured after 24 hours of incubation with isotope and 48 hours of exposure to resin. The resins were shown to significantly inhibit the synthesis of both nucleotides as compared to a heat-processed resin control. Increasing the polymerization time can mitigate the toxicity of some of the resins. The air barrier coatings used to prevent oxygen inhibition of polymerization increased the toxic effects of two resins and decreased that of one of the materials. These investigations suggest that visible light-polymerized denture resins may impair the replication of oral epithelial cells. DNA synthesis is more sensitive to the toxic effects of the materials, which may relate to the ability to cause mucosal pathology. The cytotoxic effects may relate to the presence of unpolymerized resin constituents or polymerization by-products.

Acrylic Resins↗

Relationships between denture base resin cytotoxicity and cell lipid metabolism.

Substances that elute from denture base resins may inhibit cell growth and disrupt various metabolic processes. This study investigated the effects on cell lipid metabolism of eluates from several denture base resins. Cultured oral epithelial cells were exposed in vitro to eluates of discs made from several denture base resins. Lipid metabolism of the cells was measured using isotopic labeling with 14C-acetate. Results demonstrated that the metabolism of several lipid classes found mainly in the cell membrane was altered by the resin eluates. Eluate from one resin caused the appearance of two previously unrecognized classes of lipids. The alterations of the cell lipids and the presence of the previously unrecognized lipids may be the basis for some clinically evident cytotoxic and allergic reactions.

Acrylic Resins↗