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Subsequent Response (subsequent + response)
Selected AbstractsBrowsing in a heterogeneons savannaECOGRAPHY, Issue 5 2000C. Skarpe Large herbivores generally depend on and interact with a food resource that is heterogeneous at different spatial scales. Plants allocate resources to rapid growth or to defence mechanisms depending on the availability of resources relative to loss of resources from herbivory. Herbivores select food and feeding habitats in order to maximize intake rate of nutrients and digestible energy, while avoiding chemical and structural deterrents. To optimize foraging, herbivores select habitats and food items in a hierarchical way, and different attracting and deterring factors may govern selection at different scales. We studied the impact of twig biting by a guild of indigenous browsers in three vegetation types in a semi-arid savanna in Botswana. The heaviest browsing pressure was in the vegetation type richest in preferred plant species, although that type was also richest in defended species. There were large differences in relative utilization between plant species, and ranking of species was roughly similar in the different vegetation types. Browsing pressure varied between species from almost 0-30%. Overall, spinescent trees were less browsed than non-spinescent ones, and evergreen species were less browsed than deciduous ones. In two of the three vegetation types there was a negative correlation between browsing pressure on a species and its frequency. There was a high incidence of rebrowsing, and once a tree had been browsed, the probability that it would be browsed again increased. The results largely agree with predictions based on the resource availability hypothesis, the scarcity accessibility hypothesis and recent theories on the significance of plant defences and on plant's response to browsing and the subsequent response by herbivores on the plant's responses. [source] Hypotonic stress influence the membrane potential and alter the proliferation of keratinocytes in vitroEXPERIMENTAL DERMATOLOGY, Issue 4 2007Mónika Gönczi Abstract:, Keratinocyte proliferation and differentiation is strongly influenced by mechanical forces. We investigated the effect of osmotic changes in the development of HaCaT cells in culture using intracellular calcium measurements, electrophysiological recordings and molecular biology techniques. The application of hypotonic stress (174 mOsmol/l) caused a sustained hyperpolarization of HaCaT cells from a resting potential of ,27 ± 4 to ,51 ± 9 mV. This change was partially reversible. The surface membrane channels involved in the hyperpolarization were identified as chloride channels due to the lack of response in the absence of the anion. Cells responded with an elevation of intracellular calcium concentration to hypotonic stress, which critically depended on external calcium. The presence of phorbol-12-myristate-13-acetate in the culture medium for 12 h augmented the subsequent response to hypotonic stress. A sudden switch from iso- to hypotonic solution increased cell proliferation and suppressed the production of involucrin, filaggrin and transglutaminase, markers of keratinocyte differentiation. It is concluded that sudden mechanical forces increase the proliferation of keratinocytes through alterations in their membrane potential and intracellular calcium concentration. These changes together with additional modifications in channel expression and intracellular signalling mechanisms could underlie the increased proliferation of keratinocytes in hyperproliferative skin diseases. [source] Efficacy of ciprofloxacin implants in treating experimental osteomyelitisJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2008H. Alvarez Abstract Ciprofloxacin (CFX) implants containing poly(D,L -lactide) and calcium phosphates (tricalcium phosphate and hydroxyapatite) was evaluated in 50 rabbits in an experimental osteomyelitis model. Their femoral cavity was inoculated with Staphylococcus aureus. After 2 weeks, the infected focus was cleaned out and the delivery system implanted. The infection and subsequent response to treatment were evaluated by microbiological analysis, biochemical and hematological markers, body weight, temperature, clinical signs, X-rays, and histology. Infected bone cultures, treated with CFX implants, showed reduced bacterial growth against controls. All CFX was released within 6 weeks. All animals recovered within 4 weeks. Even 12 weeks after implantation, no recurrence of infection was observed. Serum C-reactive protein, platelet, and leukocyte levels increased in all animals before treatment, and 4 weeks after it were maintained or rose in control animals, while decreased to normal levels in treated ones. Body weight was characterized by pretreatment losses, then gains during recuperation, or further loss in untreated animals; with no significant intraindividual differences in body temperature. Body weight, leucocytes, platelets, and C-reactive protein turned out to be highly useful markers for monitoring this kind of infection and its treatment. CFX implants demonstrated to be an effective therapy for S. aureus bone infection. Their efficacy was also reflected in decreasing severity of clinical signs, nonprogress of radiological signs indicative of infection, and good integration into bone structure. Histological examination revealed repair, with new bone formation extending into implants. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008 [source] Prenatal testosterone treatment potentiates the aggression-inhibiting effect of the neurosteroid dehydroepiandrosterone in female miceAGGRESSIVE BEHAVIOR, Issue 2 2001Fabrice Perché Abstract The neurosteroid dehydroepiandrosterone (DHEA) is a powerful inhibitor of aggression in murine models when given for 15 days and potentially may be useful in the management of inappropriate human aggression. Although the biosynthesis and metabolism of DHEA have been described, little is known about the potential effect of the steroidal environment during sexual differentiation on the subsequent response to DHEA. Whether prenatal androgen exposure influences the subsequent response to DHEA was assessed by comparing the effect of DHEA (80 ,g/d) on aggression in female offspring where dams were treated with 1, 10, or 100 ,g of testosterone (T) on days 15 to 18 of gestation (Experiment I) or that developed in different uterine positions (Experiment II). The results showed that DHEA decreased attack behavior in general and that the 100-,g prenatal T treatments enhanced the antiaggressive effect of this neurosteroid. Neither the lower doses of exogenously administered T nor the uterine position led to an enhanced response to DHEA. In addition, whether DHEA produced changes in social and nonsocial activities was examined. In the 100-,g T females, DHEA increased the duration of the former and decreased the frequency and duration of the latter, indicating that it was not a general decrement in behavioral expression that mediated the enhanced response to the antiaggressive effect of DHEA. In the second experiment, DHEA treatment led to increased frequencies of social nonaggressive and nonsocial activities. However, the uterine positions × treatment interactions were not significant, demonstrating that contiguity to male fetuses did not differentially affect the response to DHEA. Aggr. Behav. 27:130,138, 2001. © 2001 Wiley-Liss, Inc. [source] Sperm binding to the human zona pellucida and calcium influx in response to GnRH and progesteroneANDROLOGIA, Issue 5 2002P. Morales Summary. In this study the effect of the sequential exposure of spermatozoa to progesterone and gonadotrophin-releasing hormone (GnRH) upon zona binding and the intracellular free Ca2+ concentration was evaluated. Sperm aliquots were treated as follows: (a) 0.7 ,mol 1,1 progesterone or 0.1% DMSO (progesterone solvent) followed by 50 nmol 1,1 of GnRH; (b) 50 nmol 1,1 of GnRH or distilled water (GnRH solvent) followed by 0.7 ,mol 1,1 of progesterone. Additional aliquots were incubated with DMSO or distilled water (controls) and with 0.7 ,mol 1,1 of progesterone or 50 nmol 1,1 of GnRH. All treatments were for 5 min. Motile spermatozoa were incubated in modified Tyrode's medium, at 37 °, 5% CO2, 10times106 spermatozoa ml,1, for 4.5 h. Intracellular Ca2+ concentration and sperm-zona binding was evaluated using fura 2 and the hemizona assay, respectively. GnRH and progesterone increased sperm-zona binding and the Ca2+ concentration. Regarding zona binding, the effect of GnRH was significantly greater when the spermatozoa had been previously treated with progesterone (progesterone , GnRH = 185 ± 116 zona-bound spermatozoa versus DMSO , GnRH = 99 ± 15, P <0.001). On the other hand, previous treatment with GnRH did not modify their subsequent response to progesterone (GnRH , progesterone = 114 ±19 zona-bound spermatozoa versus distilled water , progesterone = 108 ± 22, NS). The results regarding intracellular Ca2+ showed a similar pattern. These findings suggest a priming effect of progesterone upon a GnRH-induced increase in sperm-zona binding and intracellular Ca2+. [source] Insulin release and suppression by tacrolimus, rapamycin and cyclosporin A are through regulation of the ATP-sensitive potassium channelDIABETES OBESITY & METABOLISM, Issue 6 2001D. K. Fuhrer Summary Aim By focusing on the pancreatic , cell response to tacrolimus, cyclosporin A (CsA) and rapamycin we hoped to identify immunophilin, calcineurin and/or novel mechanism involvement and advance the understanding of immunosuppressant regulated insulin control. Methods A glucose responsive , cell model was established in which the glucose response was blocked by immunosuppressant treatment and this model was used to further characterise this effect. Quantification of insulin release to immunosuppressants and specific inhibitors was used to identify the mechanism involved. Results It was found that upon the addition of tacrolimus, rapamycin, or CsA, rapid and significant exocytosis of cellular insulin was seen. A dose response study of this effect revealed optimal concentration windows of 50, 80 nm for tacrolimus, 100,300 nm for rapamycin, and 7,12 mm for CsA in RIN-5F cells. Optimal insulin release for HIT-T15 cells was similar. Additional experiments demonstrate that immunosuppressant pretreatment blocked the subsequent immunosuppressant induced insulin release but not that of a thapsigargin control, suggesting that suppression and release are non-toxic, specific and in the same pathway. Further experiments showed that this insulin release was a calcium dependent process, which was blocked by inhibitors of l -type calcium channels. Continued studies showed that the specific ATP-sensitive potassium channel agonist diazoxide (150 mm) also blocked immunosuppressant-induced insulin release. Conclusions A model that fits this data is a novel calcineurin-independent immunophilin mediated partial closing of the ATP-sensitive potassium channel, which would lead to an initial insulin release but would reduce subsequent responses through this pathway. [source] Two distinct P2Y receptors are involved in purine- and pyrimidine-evoked Ca2+ elevation in mammalian brain astrocytic culturesDRUG DEVELOPMENT RESEARCH, Issue 1-2 2001Chiara Bolego Abstract ATP and 2-methyl-thio-ATP (2-Me-SATP) increase cytosolic calcium concentrations ([Ca2+]i) in rat striatal astrocytes (Centemeri et al. [1997] Br J Pharmacol 121:1700,1706). The aim of the present study was to: (1) characterize pyrimidine-induced [Ca2+]i increases in the same experimental system, and (2) try to identify the multiple P2Y receptor subtypes mediating Ca2+ mobilization. UDP and UTP triggered a concentration-dependent [Ca2+]i elevation (EC50s = 0.58 ,M ± 0.4 and 31 ,M ± 6, respectively). Pyrimidine-evoked [Ca2+]i elevation was solely due to mobilization from intracellular stores, because: (1) removing calcium from extracellular medium or (2) blocking its influx with Ni2+ did not modify UTP responses; (3) the store-depleting agent thapsigargin completely abolished UTP-evoked [Ca2+]i increments. Guanosine-5,-O-(2-thiodiphosphate) partially inhibited the UTP response, whereas pertussis toxin (PTx) had no effect. The phospholipase C inhibitor U-73122 significantly reduced the UTP-evoked [Ca2+]i rise. Computer-assisted analysis indicated that the UTP and UDP responses are mediated by a single receptor, while ATP and 2-Me-SATP interact with two distinct receptors. The selective P2Y1 receptor antagonist MRS2179 abolished the ATP higher potency component. Sequential challenges with the same nucleotides resulted in almost complete homologous desensitization. Pre-exposure to UTP lowered the subsequent responses to either ATP or 2-Me-SATP. Maximally active concentrations of UTP and ATP were not additive. In conclusion, [Ca2+]i elevation in astrocytes by purines and pyrimidines is mediated by two distinct P2Y receptors, likely the P2Y1 and P2Y6 subtypes. Drug Dev. Res. 52:122,132, 2001. © 2001 Wiley-Liss, Inc. [source] Annulus cells release ATP in response to vibratory loading in vitroJOURNAL OF CELLULAR BIOCHEMISTRY, Issue 4 2003Satoru Yamazaki Abstract Mechanical forces regulate the developmental path and phenotype of a variety of tissues and cultured cells. Vibratory loading as a mechanical stimulus occurs in connective tissues due to energy returned from ground reaction forces, as well as a mechanical input from use of motorized tools and vehicles. Structures in the spine may be particularly at risk when exposed to destructive vibratory stimuli. Cells from many tissues respond to mechanical stimuli, such as fluid flow, by increasing intracellular calcium concentration ([Ca2+]ic) and releasing adenosine 5,-triphosphate (ATP), extracellularly, as a mediator to activate signaling pathways. Therefore, we examined whether ATP is released from rabbit (rAN) and human (hAN) intervertebral disc annulus cells in response to vibratory loading. ATP release from annulus cells by vibratory stimulation as well as in control cells was quantitated using a firefly luciferin-luciferase assay. Cultured hAN and rAN cells had a basal level of extracellular ATP ([ATP]ec) in the range of 1,1.5 nM. Vibratory loading of hAN cells stimulated ATP release, reaching a net maximum [ATP] within 10 min of continuous vibration, and shortly thereafter, [ATP] declined and returned to below baseline level. [ATP] in the supernatant fluid of hAN cells was significantly reduced compared to the control level when the cells received vibration for longer than 15 min. In rAN cells, [ATP] was increased in response to vibratory loading, attaining a level significantly greater than that of the control after 30 min of continuous vibration. Results of the current study show that resting annulus cells secrete ATP and maintain a basal [ATP]ec. Annulus cells may use this nucleotide as a signaling messenger in an autocrine/paracrine fashion in response to vibratory loading. Rapid degradation of ATP to ADP may alternatively modulate cellular responses. It is hypothesized that exposure to repetitive, complex vibration regimens may activate signaling pathways that regulate matrix destruction in the disc. As in tendon cells, ATP may block subsequent responses to load and modulate the vibration response. Rabbit annulus cells were used as a readily obtainable source of cells in development of an animal model for testing effects of vibration on the disc. Human cells obtained from discarded surgical specimens were used to correlate responses of animal to human cells. © 2003 Wiley-Liss, Inc. [source] Proactive consumer consultation: the effect of information provision on response to transgenic animalsJOURNAL OF PUBLIC AFFAIRS, Issue 3-4 2005David Castle A national study is reported which proactively engaged 1365 Canadian consumers and solicited their opinions concerning new transgenic salmon and pork products which have not yet entered the marketplace. Respondents were methodically requested to provide initial free-association responses, and then scaled responses to product concepts about which progressively more information was revealed. This combined qualitative and quantitative method was pursued in order to determine initial knowledge levels and subsequent responses with a minimal amount of cueing via question probes. The results indicate that disclosure concerning benefits and risks of these new technologies did not harm judgements about them or estimates of purchase intent. A significant determinant of opinions was the gender of the respondent. Females were more negatively predisposed overall to the concepts and more sensitive to specific information regarding product benefits and risks. The research offers a methodological template for public consultation and communication pre-testing for new biotechnological products. Implications for regulatory policy and information dissemination for new food biotechnology products are discussed. Copyright © 2005 John Wiley & Sons, Ltd. [source] Training the forgetting of negative words: The role of direct suppression and the relation to stress reactivityAPPLIED COGNITIVE PSYCHOLOGY, Issue 3 2010Joelle LeMoult Recent research has demonstrated that people can be trained to forget negative material. This experiment assessed the possible benefit of direct suppression in addition to the benefit of thought substitutes (indirect suppression) on subsequent attempts to recall words. We also investigated the association between recall following suppression training and subsequent responses to an acute laboratory stressor. After learning cue-target word pairs, participants completed a training phase in which they practiced suppressing targets and recalling substitutes or simply recalling substitutes with no instruction to suppress. Our results show similar effects of suppression condition on forgetting. Importantly, however, the absence of direct suppression predicted mood change in response to a subsequently presented laboratory stressor. These results suggest that direct suppression is not necessary for forgetting to occur, but it seems to protect against negative emotional consequences of interference-induced forgetting. Copyright © 2010 John Wiley & Sons, Ltd. 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