19 research outputs found
Topical Analgesia with Lidocaine Plus Diclofenac Decreases Pain in Benign Anorectal Surgery: Randomized, Double-blind, and Controlled Clinical Trial
Objective: The aim of this study is to evaluate the efficacy and safety of a topical formulation containing lidocaine plus diclofenac (CLIFE1) compared to CLIFE2 (lidocaine), to decrease pain in benign anorectal surgery (BARS) to date not evaluated. Background: More than 50% of patients undergoing BARS, especially hemorrhoidectomy, suffer from moderate and severe postoperative pain. This remains an unresolved problem that could be addressed with the new CLIFE1 topical treatment. Methods: A multicenter, randomized double-blind, active-controlled parallel-group superiority trial, was conducted in two Spanish hospitals. Patients undergoing BARS (hemorrhoids, anal fistula and anal fissure) were randomized at the end of surgery at a 1:1 ratio to receive first dose either CLIFE1 (n=60) or CLIFE2 (n=60) anorectal topical treatment, and after every 12 hours for the first three postoperative days and once a day from the fourth to sixth. The primary outcome was average of pain decrease after topical treatment, measured with visual analogue scale (VAS) by the patients themselves, the evening in the surgery day and four times daily for the first three postoperative days. Results: The results of 120 patients included out of 150 selected undergoing BARS show a decrease in pain after CLIFE1 topical treatment (7.47±13.2) greater than with CLIFE2 (4.38±6.75), difference -3.21 (95% CI) -5.75; -0.676; p=0.008), decreasing significantly postoperative pain (≥ 9 mm, VAS) in 35% of patients undergoing benign anorectal surgery, compared to 18.33 % treated with lidocaine. Conclusions: The CLIFE1 topical treatment shows better analgesic efficacy than CLIFE2 in BARS
Effect of temperature on pollen germination for several Rosaceae species: influence of freezing conservation time on germination patterns
[EN] Between February 2018 and April 2018, flowers were collected from eight Rosaceae species. Flowers were kept in a freezer at -20 degrees C for three freezing times (Treatment 1, two months; Treatment 2, four months; Treatment 3, six months). After extracting pollen, in vitro germination was induced in a culture medium and incubated at six different temperatures for 72 h. The percentage of pollen germination, average pollen tube length and maximum pollen tube length were measured. Pollen germination was maximum for all species between 15 degrees C and 30 degrees C. Cydonia oblonga, Malus sylvestris, Prunus avium, Prunus domestica, Prunus dulcis, Prunus persica and Pyrus communis obtained 30-52% pollen germination between 15 degrees C and 20 degrees C. Prunus cerasifera had 40% pollen germination at 30 degrees C. All species studied reached the maximum pollen tube length between 10 degrees C and 25 degrees C. Germination did not change significantly for any of the species with freezing time, but we found significant differences in the three parameters measured between treatments. The highest germination percentages were obtained in Treatment 2 (four months frozen at -20 degrees C), while the maximum pollen tube length was reached in Treatment 1 (two months frozen at -20 degrees C). According to our results, freezing time affected the germination-temperature patterns. This could indicate that studies on the effect of temperature on pollen germination should always be carried out with fresh pollen to obtain more conclusive data.This work was supported by the Asociacion Club de Variedades Vegetales Protegidas as a part of a project with the Universitat Politecnica de Valencia (UPV 20170673). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Beltrán, R.; Valls, A.; Cebrián, N.; Zornoza, C.; García-Breijo, F.; Reig Armiñana, J.; Garmendia, A.... (2019). Effect of temperature on pollen germination for several Rosaceae species: influence of freezing conservation time on germination patterns. PeerJ. 7:1-18. https://doi.org/10.7717/peerj.8195S1187Acar, I., & Kakani, V. G. (2010). The effects of temperature on in vitro pollen germination and pollen tube growth of Pistacia spp. Scientia Horticulturae, 125(4), 569-572. doi:10.1016/j.scienta.2010.04.040Boavida, L. C., & McCormick, S. (2007). TECHNICAL ADVANCE: Temperature as a determinant factor for increased and reproducible in vitro pollen germination in Arabidopsis thaliana. The Plant Journal, 52(3), 570-582. doi:10.1111/j.1365-313x.2007.03248.xBrewbaker, J. L., & Kwack, B. H. (1963). THE ESSENTIAL ROLE OF CALCIUM ION IN POLLEN GERMINATION AND POLLEN TUBE GROWTH. American Journal of Botany, 50(9), 859-865. doi:10.1002/j.1537-2197.1963.tb06564.xBurke, J. J., Velten, J., & Oliver, M. J. (2004). In Vitro Analysis of Cotton Pollen Germination. Agronomy Journal, 96(2), 359-368. doi:10.2134/agronj2004.3590Castède, S., Campoy, J. A., García, J. Q., Dantec, L., Lafargue, M., Barreneche, T., … Dirlewanger, E. (2014). Genetic determinism of phenological traits highly affected by climate change in
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flowering date dissected into chilling and heat requirements. New Phytologist, 202(2), 703-715. doi:10.1111/nph.12658Cerovlć, R., & Ružić, D. (1992). Pollen tube growth in sour cherry (Prunus cerasusL.) at different temperatures. Journal of Horticultural Science, 67(3), 333-340. doi:10.1080/00221589.1992.11516256Egea, J., Burgos, L., Zoroa, N., & Egea, L. (1992). Influence of temperature on thein vitrogermination of pollen of apricot(Prunus armeniaca, L.). Journal of Horticultural Science, 67(2), 247-250. doi:10.1080/00221589.1992.11516244Fan, L.-M. (2001). In vitro Arabidopsis pollen germination and characterization of the inward potassium currents in Arabidopsis pollen grain protoplasts. Journal of Experimental Botany, 52(361), 1603-1614. doi:10.1093/jexbot/52.361.1603Feij�, J. A., Malh�, R., & Obermeyer, G. (1995). Ion dynamics and its possible role during in vitro pollen germination and tube growth. Protoplasma, 187(1-4), 155-167. doi:10.1007/bf01280244Goldwin, G. K., & Webster, A. D. (1983). The cumulative effects of hormone mixtures containing GA3, DPU plus NOXA, NAA or 2,4,5-TP on the cropping and flowering of sweet cherry cultivars,Prunus aviumL. Journal of Horticultural Science, 58(4), 505-516. doi:10.1080/00221589.1983.11515149Hebbar, K. B., Rose, H. M., Nair, A. R., Kannan, S., Niral, V., Arivalagan, M., … Vara Prasad, P. V. (2018). Differences in in vitro pollen germination and pollen tube growth of coconut (Cocos nucifera L.) cultivars in response to high temperature stress. Environmental and Experimental Botany, 153, 35-44. doi:10.1016/j.envexpbot.2018.04.014Hedhly, A., Hormaza, J. I., & Herrero, M. (2004). Effect of temperature on pollen tube kinetics and dynamics in sweet cherry,Prunus avium(Rosaceae). American Journal of Botany, 91(4), 558-564. doi:10.3732/ajb.91.4.558Hedhly, A., Hormaza, J. I., & Herrero, M. (2005). The Effect of Temperature on Pollen Germination, Pollen Tube Growth, and Stigmatic Receptivity in Peach. Plant Biology, 7(5), 476-483. doi:10.1055/s-2005-865850Hegedűs, A., & Halász, J. (2006). Self-incompatibility in plums (Prunus salicina Lindl., Prunus cerasifera Ehrh. and Prunus domestica L.). A minireview. International Journal of Horticultural Science, 12(2). doi:10.31421/ijhs/12/2/646Hegedűs, A., Lénárt, J., & Halász, J. (2012). Sexual incompatibility in Rosaceae fruit tree species: molecular interactions and evolutionary dynamics. Biologia plantarum, 56(2), 201-209. doi:10.1007/s10535-012-0077-3Heide, O. M., & Prestrud, A. K. (2005). Low temperature, but not photoperiod, controls growth cessation and dormancy induction and release in apple and pear. Tree Physiology, 25(1), 109-114. doi:10.1093/treephys/25.1.109Iglesias, A., Garrote, L., Quiroga, S., & Moneo, M. (2011). A regional comparison of the effects of climate change on agricultural crops in Europe. Climatic Change, 112(1), 29-46. doi:10.1007/s10584-011-0338-8KAKANI, V. G., PRASAD, P. V. V., CRAUFURD, P. Q., & WHEELER, T. R. (2002). Response of in vitro
pollen germination and pollen tube growth of groundnut (Arachis hypogaea
L.) genotypes to temperature. Plant, Cell & Environment, 25(12), 1651-1661. doi:10.1046/j.1365-3040.2002.00943.xKAKANI, V. G., REDDY, K. R., KOTI, S., WALLACE, T. P., PRASAD, P. V. V., REDDY, V. R., & ZHAO, D. (2005). Differences in in vitro Pollen Germination and Pollen Tube Growth of Cotton Cultivars in Response to High Temperature. Annals of Botany, 96(1), 59-67. doi:10.1093/aob/mci149Mesejo, C., Martínez-Fuentes, A., Reig, C., Rivas, F., & Agustí, M. (2006). The inhibitory effect of CuSO4 on Citrus pollen germination and pollen tube growth and its application for the production of seedless fruit. Plant Science, 170(1), 37-43. doi:10.1016/j.plantsci.2005.07.023Pham, V. T., Herrero, M., & Hormaza, J. I. (2015). Effect of temperature on pollen germination and pollen tube growth in longan ( Dimocarpus longan Lour.). Scientia Horticulturae, 197, 470-475. doi:10.1016/j.scienta.2015.10.007Reddy, K. R., & Kakani, V. G. (2007). Screening Capsicum species of different origins for high temperature tolerance by in vitro pollen germination and pollen tube length. Scientia Horticulturae, 112(2), 130-135. doi:10.1016/j.scienta.2006.12.014Rosell, P., Herrero, M., & Galán Saúco, V. (1999). Pollen germination of cherimoya (Annona cherimola Mill.). Scientia Horticulturae, 81(3), 251-265. doi:10.1016/s0304-4238(99)00012-6Sanzol, J., & Herrero, M. (2001). The «effective pollination period» in fruit trees. Scientia Horticulturae, 90(1-2), 1-17. doi:10.1016/s0304-4238(00)00252-1Saxe, H., Cannell, M. G. R., Johnsen, Ø., Ryan, M. G., & Vourlitis, G. (2001). Tree and forest functioning in response to global warming. New Phytologist, 149(3), 369-399. doi:10.1046/j.1469-8137.2001.00057.xSedgley, M. (1977). The Effect of Temperature on Floral Behaviour, Pollen Tube Growth and Fruit Set in the Avocado. Journal of Horticultural Science, 52(1), 135-141. doi:10.1080/00221589.1977.11514739Silva, G. J., Souza, T. M., Barbieri, R. L., & Costa de Oliveira, A. (2014). Origin, Domestication, and Dispersing of Pear (Pyrusspp.). Advances in Agriculture, 2014, 1-8. doi:10.1155/2014/541097Sorkheh, K., Azimkhani, R., Mehri, N., Chaleshtori, M. H., Halász, J., Ercisli, S., & Koubouris, G. C. (2018). Interactive effects of temperature and genotype on almond ( Prunus dulcis L.) pollen germination and tube length. Scientia Horticulturae, 227, 162-168. doi:10.1016/j.scienta.2017.09.037Sorkheh, K., Shiran, B., Rouhi, V., & Khodambashi, M. (2011). Influence of temperature on the in vitro pollen germination and pollen tube growth of various native Iranian almonds (Prunus L. spp.) species. Trees, 25(5), 809-822. doi:10.1007/s00468-011-0557-7Sorkheh, K., Shiran, B., Rouhi, V., Khodambashi, M., Wolukau, J. N., & Ercisli, S. (2011). Response of in vitro pollen germination and pollen tube growth of almond (Prunus dulcis Mill.) to temperature, polyamines and polyamine synthesis inhibitor. Biochemical Systematics and Ecology, 39(4-6), 749-757. doi:10.1016/j.bse.2011.06.015Stern, R. A., Goldway, M., Zisovich, A. H., Shafir, S., & Dag, A. (2004). Sequential introduction of honeybee colonies increases cross-pollination, fruit-set and yield of ‘Spadona’ pear (Pyrus communisL.). The Journal of Horticultural Science and Biotechnology, 79(4), 652-658. doi:10.1080/14620316.2004.11511821Webster, A. D., & Goldwin, G. K. (1981). The hormonal requirements for improved fruit setting of plum,Prunus domesticaL. cv Victoria. Journal of Horticultural Science, 56(1), 27-40. doi:10.1080/00221589.1981.11514962Weinbaum, S. A., Parfitt, D. E., & Polito, V. S. (1984). Differential cold sensitivity of pollen grain germination in two Prunus species. Euphytica, 33(2), 419-426. doi:10.1007/bf00021139Wickham, H. (2016). ggplot2. Use R! doi:10.1007/978-3-319-24277-4Wolukau, J. N., Zhang, S., Xu, G., & Chen, D. (2004). The effect of temperature, polyamines and polyamine synthesis inhibitor on in vitro pollen germination and pollen tube growth of Prunus mume. Scientia Horticulturae, 99(3-4), 289-299. doi:10.1016/s0304-4238(03)00112-
Is the pollination efficiency of long-lived orchid flowers affected by age?
The long-lived flowers of orchids increase the chances of pollination and thus the reproductive success of the species. However, a question arises: does the efficiency of pollination, expressed by fruit set, vary with the flower age? The objective of this study was to verify whether the flower age of Corymborkis flava(Sw.) Kuntze affects pollination efficiency. The following hypotheses were tested: 1) the fruit set of older flowers is lower than that of younger ones; 2) morphological observations (perianth and stigmatic area), stigma receptivity test by using a solution of hydrogen peroxide and hand-pollination tests are equally effective in defining the period of stigmatic receptivity. Flowers were found to be receptive from the first to the fourth day of anthesis. Fruit set of older flowers (third and fourth day) was lower than that of younger flowers. Morphological observations, the stigma receptivity test and hand-pollinations were equally effective in defining the period of stigmatic receptivity. However, to evaluate the maximum degree of stigma receptivity of orchid species with long-lived flowers, we recommend hand-pollinations, beyond the period of receptivity