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Notes: Tetracyclines have been widely used as adjuncts in periodontal therapy due to the antimicrobial efficacy of these drugs. Recently, their ability to inhibit host-derived matrix metalloproteinases (collagenase and gelatinase) and bone resorption in organ culture has also been invoked as a therapeutic rationale. The current study was undertaken to determine whether tetracyclines can inhibit alveolar bone loss in vivo due to a non-antimicrobial action of these drugs. Experimental periodontitis was induced by inoculating adult, male Sprague-Dawley rats with P. gingivalis (strain 381) following kanamycin/ampicillin pretreatment. Doxycycline, non-antimicrobial chemically-modified tetracycline (CMT-1) and vehicle alone were administered daily to 3 infected groups of rats (n=6 rats per group; each group housed in a sterilized inflatable isolator) beginning 10 days after P. gingivalis inoculation. The control group (n = 6; non-infected rats) received only vehicle. After 5 weeks of daily drug administration by gastric intubation, the experiment was terminated and blood samples were taken from each animal to determine antibody levels against P. gingivalis. Plaque samples were collected from each group of animals before and after P. gingivalis inoculation and at the end of the experiment for microbiological examination. The jaws were removed from each rat, defleshed and then analyzed morphometrically and radiographically to assess bone loss. Serum antibody levels against P. gingivalis were significantly elevated in the 3 infected groups compared to the non-infected controls. This, together with the microbiologic findings, indicated that these groups of rats were infected with P. gingivalis. Significantly greater bone loss was observed in the untreated P. gingivalis-infected group compared to the controls based on both morphometric and radiographic measurements. Oral administration of doxycycline or CMT-1 to the P. gingivalis-infected rats completely inhibited this bone loss. As expected, CMT-1 did not exhibit an antimicrobial effect against P. gingivalis. Therefore, this study indicates that tetracyclines can inhibit alveolar bone loss in vivo by a mechanism which is independent of the antimicrobial efficacy of these drugs.

Notes: Experimental diabetes in the rat rapidly produces a shift in the gingival crevicular microflora which is followed, within weeks, by increased production of collagenase by the gingival tissues. To assess the contribution of endogenous (hormonal or metabolic) and exogenous (altered crevicular microflora) factors on this diabetes-induced abnormality in collagenase production, the following series of experiments was undertaken: In each experiment, the germfree rats were housed in two isolators. Half of the animals in both isolators were rendered diabetic (D) with streptozotocin while the remainder were left untreated (non-diabetic (ND) controls). All of the germfree ND and D rats in one isolator of the pair were then infected with either a Gram-positive (S. mitis or A. odontolyticus) or a Gram-negative (Capnocytophaga, A. aclmomycetemcomitans or B. gingivalis) organism. In the other isolator, the ND and D rats were maintained in their germfree state. After 3 wk, the germfree and monoinfected rats were killed and the gingiva (and in one experiment, skin) were dissected. Collagenase activity produced by gingiva in culture (or extracted from gingiva or from skin) was measured using 14C-collagen fibrils (or [3Hmethyl] collagen molecules) as the substrate. Diabetes increased the collagenolytic activity in the gingiva and skin of the germfree rats. Infecting the germfree rats with a Gram-positive organism had no effect on collagenase activity generated by the gingival explants in the tissue culture system. In contrast, infection with any of the Gram-negative organisms dramatically increased the collagenase activity in the gingival tissues of the ND rats in culture, an effect not seen in the D group of rats using this system. However, monoinfection with B. gingivalis did increase collagenase activity in the extracts of gingiva (but not in skin) from both ND and D rats, with the latter group showing the highest level of enzyme activity. We suggest (i) that experimental diabetes stimulates collagenase production in gingiva by both endogenous (hormonal) and exogenous (bacterial) mechanisms, and (ii) that crevicular Gram-negative organisms stimulate collagenolysis in the adjacent gingival tissues by releasing bacterial products (e.g. endotoxins) which penetrate into the connective tissue and enhance host cell collagenase production.

Notes: Abstract  A three-electrode capacitive pressure sensor for touch-mode operation with sensitivity of 0.030 pF/kPa (or 10.4 mV/kPa using CP-10 C/V converter circuit) in the pressure range of 170–280 kPa is presented with theoretical explanation of experimental results. A special ring structure is designed to integrate a sensing capacitor and a reference capacitor into the same cavity to partially cancel out the temperature effect. A third electrode is included to eliminate two-level connections without reducing its pressure sensitivity. The sensor offers the advantages of simple fabrication processes, planar connections, as well as high sensitivity, near-linear output, and large over-range pressure.

Notes: Abstract Melt spinning of a nickel-base superalloy containing various amounts of boron up to 3.0 wt% has been carried out to explore the potential of extended boride alloyability through rapid solidification. More specifically, the melt-spinning castability, ribbon-solidification microstructure and heat-treatment precipitation were studied as a function of boron concentration by using analytical electron microscopy and a number of other techniques. Special attention was given to the boride structure, chemistry and thermal stability. The microstructural observations were then correlated to the ribbon bend ductility tested in as-cast and annealed conditions. On the basis of the present results, future investigation of superalloys using the rapid solidification process and the boride alloying concept is discussed.