A new type of hydrogel capable of sol-gel phase-reversible transition by changes in the environmental glucose concentration has been synthesized. The hydrogel consists of vinylpyrrolidinone-allylglucose (VP/AG) copolymer and concanavalin A (Con A). The formation of the hydrogel is based on the specific interaction between glucose on the copolymer and glucose receptor sites on Con A. Hydrogels were formed immediately after mixing the copolymer and Con A. The critical factors in the formation of hydrogel were the concentrations of the copolymer, of glucose on the copolymer and of Con A. In general, the formation of a hydrogel became more efficient as the concentration of glucose on the copolymer decreased and/or as the Con A concentration increased. The hydrogel formed became a sol in the presence of glucose in the environment. The environmental glucose concentration necessary to dissolve the gel to sol was approximately four times higher than the concentration of glucose on the copolymer. Upon removal of the environmental glucose by dialysis, the sol became a gel again and the sol-gel phase transition could be repeated.

Concanavalin A↗

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Acute surface-induced thrombosis in the canine ex vivo model: importance of protein composition of the initial monolayer and platelet activation.

The initial events occurring at the blood-polymer interface were examined using a canine ex vivo arteriovenous shunt model. Thrombogenic (fibrinogen) and nonthrombogenic (albumin) proteins were preadsorbed on poly(vinyl chloride), polyethylene, and silicone rubber shunt surfaces, and the blood responses were analyzed using the platelet deposition profile as an indicator of surface thrombogenicity. The distributions of preadsorbed protein molecules on the various polymer surfaces were studied using an immunogold bead (colloidal gold particles coated with antibodies) staining technique and shown to be homogeneous. A sequential protein adsorption technique was developed to probe the nature of competitive protein adsorption and to observe the effect of surface protein concentration on thrombogenicity. The thrombogenicity of a surface was determined by the composition of the initial protein layer rather than the total concentration of protein on the polymer surfaces. The composition of this layer determines the extent of platelet activation and the adhesive strength between platelets and the polymer surface.

Adsorption↗

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Developmental anatomy of the eustachian tube and middle ear in mice.

PURPOSE: It is generally accepted that the development of the tubotympanum has significant bearing on the susceptibility to ear infection. A detailed study of the differentiation of ciliated cells in secretory elements will be useful in understanding both the normal physiology and the pathology of the tubotympanum. METHOD: Serially sectioned temporal bones of 76 mice ranging from gestational age day 11 to postnatal day 21 were examined microscopically. RESULTS: During the period of gestation, the tubotympanic recess was formed at the 12th day and began to extend to form the middle ear between the 13th and 14th days. A rapid increase in the volume of the tubotympanic recess was observed between the 15th and 16th days when a definitive division of the tubotympanic recess into the eustachian tube and middle ear cavity was observed. Postnatally the tubotympanum attained an adult form around day 9, and the maximum change of middle ear volume was noted on day 11, when the mesenchymal tissue in the middle ear cavity disappeared completely. Development of the ciliated cells was observed concurrently in both the eustachian tube and middle ear on the 16th gestational day, one day earlier than the appearance of the epithelial secretory cells in both the eustachian tube and middle ear. The number of ciliated cells and secretory cells increased rapidly after birth. Tubal glands were well developed with evidence of secretory activity around the time of birth. CONCLUSIONS: Based on these findings, one can conclude that the mucociliary defense system starts to develop during the fetal stage and is well established immediately after birth.

Animals↗

PubMedDate not supplied

The role of inducible nitric oxide synthase in cocaine-induced locomotor sensitization.

Experimentally naive male Sprague-Dawley rats (weighing 85-110 g) were used to examine the role of inducible nitric oxide synthase (iNOS) in cocaine-induced locomotor sensitization. Repeated administration of cocaine (15 mg/kg, ip) for 7 consecutive days produced locomotor sensitization. Pretreatment with iNOS inhibitors, L-N(6)-(1-iminoethyl) lysine (NIL) or (-)-epigallocatechin gallate (EGCG; 10 mg/kg, ip), 30 min before cocaine (15 mg/kg, ip) administration totally blocked the development of cocaine-induced locomotor sensitization. Dopamine (DA) receptor binding in the nucleus accumbens (NAC) showed a significant decrease in the density of D(2) receptor and the affinity of D(1) receptor after cocaine treatment. Pretreatment with EGCG or NIL abolished the cocaine-induced changes in these parameters. These results suggest that iNOS may participate in the process of development of locomotor sensitization through the modulation of DA receptors in the NAC.

Animals↗

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