Promotion of peri-implant bone healing by systemically administered parathyroid hormone (1-34) and zoledronic acid adsorbed onto the implant surface.

UNLABELLED: The effect of human parathyroid hormone 1-34 (PTH) and zoledronic acid (ZA) alone or in combination on bone healing in osteoporotic settings was tested using implants inserted in tibiae of ovariectomized (OVX) rats. Combination therapy promoted bone healing more than each treatment alone 12 weeks after implant insertion. INTRODUCTION: PTH and ZA have been demonstrated to be effective on implant fixation. However, reports about the combined use of PTH and ZA for promotion of bone healing around implant in osteoporotic settings are still limited. This study aims to investigate effects of PTH+ZA on implant stabilization in OVX rats. METHODS: Twelve weeks after bilateral ovariectomy, OVX rats randomly received implants without or with ZA (by immersion in 1 mg/ml ZA solution for 24 h). Subsequently, half of the animals from each group also received subcutaneous injections of PTH (60 µg/kg, three times a week) for 12 weeks. Thus, there were four groups: control, PTH, ZA, and PTH+ZA. RESULTS: All treatments promoted bone healing around implant compared to control, but PTH+ZA treatment showed significantly stronger effects than PTH or ZA alone in histological, micro-CT, and biomechanical tests. CONCLUSION: The results indicated the additive effects of PTH and ZA on implant fixation in OVX rats; it was suggested that the anabolic effect of PTH was potent and not blunted by ZA during bone healing around implant when used concurrently.

Yolk sac tumour involving floor of mouth: case report.

Yolk sac tumour is a rare malignant tumour of germ cell origin that usually arises from the gonads. It is extremely rare in the head and neck. We present a case of a yolk sac tumour that involved the floor of the mouth in a 14-month-old Chinese girl. The diagnosis was confirmed by histological examination that showed characteristic Schiller-Duval bodies, and immunohistochemical examination that showed α-fetoprotein being expressed within the cytoplasm of the neoplastic cells. The patient died 4 months postoperatively. To our knowledge, this is the first case of a yolk sac tumour of the floor of mouth that has been reported in an English journal.

Novel mutation breeding method for Streptomyces avermitilis using an atmospheric pressure glow discharge plasma.

AIMS: Avermectins are major antiparasitic agents used commercially in animal health, agriculture and human infections. To improve the fermentation efficiency of avermectins, for the first time a plasma jet generated by a novel atmospheric pressure glow discharge (APGD) was employed to generate mutations in Streptomyces avermitilis. METHODS AND RESULTS: The APGD plasma jet, driven by a radio frequency (RF) power supply with water-cooled and bare-metallic electrodes, was used as a new mutation method to treat the spores of S. avermitilis. The plasma jet yielded high total (over 30%) and positive (about 21%) mutation rates on S. avermitilis, and a mutated strain, designated as G1-1 with high productivity of avermectin B1a and genetic stability, was obtained. CONCLUSIONS: Because of the low jet temperature, the high concentrations of the chemically reactive species and the flexibility of its operation, the RF APGD plasma jet has a strong mutagenic effect on S. avermitilis. SIGNIFICANCE AND IMPACT OF THE STUDY: This is a proof-of-concept study for the use of an RF APGD plasma jet for inducing mutations in microbes. We have shown that the RF APGD plasma jet could be developed as a promising and convenient mutation tool for the fermentation industry and for use in biotechnology research.

The effect of surface composition of titanium films on bacterial adhesion.

We show that bacterial adhesion on titanium (Ti) films could be radically minimized by tailoring the surface chemical stoichiometry of the films. Using a dc magnetron sputtering system, Ti films with various surface compositions, such as oxide and nitride combinations, were prepared by controlling processing parameters such as cathode power, sputtering pressure and base vacuum. The surface topography of the films was observed to be smooth and similar in all the films prepared under different conditions. The order of adhesion of the oral bacterial Porphyromonas gingivalis varied with the surface chemical stoichiometry of the Ti films. Few surface stoichiometries of typical oxide nitride combination resulted in nearly nil bacterial adhesion.

[Determination of the progesterone antagonist lilopristone in serum by RP-HPLC].

To 1.0 ml of serum containing lilopristone were added RU486 solution (internal standard, IS) and 1 ml of 1.0 mol.L-1 NaOH. The mixture was extracted with diethyl ether for 2 times. After extraction, the combined organic phase was evaporated to dryness and the residue was dissolved in the mobile phase and washed with petroleum ether. After centrifugation, 20 microliters of the lower layer was subjected to HPLC. A muBondapak-C18 (10 microns) column (30 cm x 3.9 mm) was used and the column temperature was kept at 50 degrees C. The flow rate of mobile phase (methanol-dichloromethane--0.01 mol.L-1 phosphate buffer, pH 4.0, 67:5:28 v/v) was 1.1 ml.min-1 and UV detection was performed at 302 nm. The retention times of lilopristone and IS were 6.85 and 9.07 min respectively and the detection limit was 10 ng.ml-1 (S/N > or = 4) serum. The extraction recoveries of lilopristone and IS were over 85%. The relative standard deviations were 2.21 to 4.23%. This method has been applied to study the pharmacokinetic of lilopristone in rats.

Molecular analysis of hypoxanthine phosphoribosyltransferase gene deletions induced by alpha- and X-radiation in human lymphoblastoid cells.

Mutations caused by exposure to X-radiation and to radon and its decay products were compared in the hprt gene of a human lymphoblastoid cell line. Thirty-one X-radiation-induced, 29 radon-induced, and 24 spontaneous mutants were recovered from cell cultures under identical conditions except for the exposure to radiation. Seven spontaneous point mutations were recovered and DNA sequenced. These mutations included three C:G-->T:A transitions. These spontaneous point mutations were located in the exon or splice donor regions of five of the nine hprt exons. Four X-radiation-induced and three radon-induced point mutations were also analyzed by DNA sequencing. The frequency of induced mutants at the D0 doses for radon and X-radiation respectively were 5 x 10(-6) and 4.5 x 10(-6). Deletions were the predominant mutations recovered from both radon- and X-irradiated cells. Eighty-one percent of the mutants from X-radiation-treated cultures, 86% of the radon-treated cultures, and 63% of the spontaneous mutants involved deletions. Deletions involving exon and intron DNA, as well as intron DNA alone, were found to inactivate the hprt gene and result in a selectable HPRT- phenotype. Among the deletion mutants, however, only 21% of the spontaneous mutants versus 55% of both the X-radiation- and radon-induced mutants exhibited loss of the entire hprt gene. More X-radiation-induced deletions than radon-induced deletions extended further than 800 bp in the telomeric direction from the hprt gene (six of 17 versus two of 17). The results show that at the human hprt locus of TK-6 cells the predominant kind of mutation indicative of exposure to both high LET alpha-radiation and low LET X-radiation is a large deletion, spanning the entire hemizygous hprt gene and extending into flanking sequences.

Sequencing of double-stranded polymerase chain reaction products for mutation analysis.

This report describes a reproducible, straightforward approach to sequencing double-stranded DNA products from the polymerase chain reaction (PCR) for analysis of mutations. The sequencing protocol is a modification of that published by Kretz (Kretz et al., 1989) and has been successful in the hands of a number of investigators working on diverse projects. Following this procedure, PCR DNA products generated from bacterial sources (including pBR322 and F' derivatives), as well as cDNA and genomic DNA from both hamster and human cell lines, have been sequenced with equal success. Close attention to the molar ratio of nucleotides to double-stranded DNA template present during the labeling reaction ensures best results.

[Interceptive activity of epostane in pregnant rats and rhesus monkeys].

A complete interceptive action on pregnancy was shown after ig epostane (Epo) 48 and 96 mg/kg on d 10 of pregnancy in rats. ED50 (95% fiducial limits) of Epo was 20.7 (16.3-26.3) mg/kg. Epo 48 mg/kg ig on d12, 14 and 16 of pregnancy lowered rat plasma progesterone concentrations (P less than 0.05) and plasma corticosterone on d 16 of pregnancy (P less than 0.05). Epo 35 mg/(kg.d) was given ig on d 50-54 of pregnancy in rhesus monkeys. Vaginal bleeding was seen in all of the 6 treated monkeys. Complete expulsions of fetal and placental materials occurred in 5 of the treated monkeys, among which 2 aborted on d 53 and the other 3 on d 54 of pregnancy. Plasma progesterone concentrations of the treated monkeys were lowered on d 52, 53 and 54 of pregnancy (P less than 0.05) and plasma estradiol on d 51, 52, 53, 54 and 55 (P less than 0.05), while there were no significant differences in plasma hydrocortisone. Epo may be a valuable supplement to the existing methods of female contraception.

Effects of forelimb amputation and denervation on protein synthesis in spinal cord ganglia of the newt.

Analysis of the effects of forelimb amputation and denervation on [35S]methionine incorporation into the protein of newt brachial plexus nerve ganglia showed that amputation increases the level of protein synthesis about 4-fold as compared with that of control (nonamputated) animals. Denervation without amputation nearly doubles the level of protein synthesis as compared with controls. Analysis of labeled protein by means of two-dimensional gel electrophoresis and radioautogram revealed incorporation patterns that are similar to controls; this observation suggests that amputation affects nerve cells quantitatively rather than qualitatively, in influencing the production of putative neurotrophic agents. A group of basic proteins ranging in Mr from 15,000 to 31,000 are prominently expressed in these radioautograms from experimental ganglia and may be important in promoting forelimb regeneration in the newt.