974 resultados para hemoglobin A2


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Heme metabolism is central to malaria parasite biology. The parasite acquires heme from host hemoglobin in the intraerythrocytic stages and stores it as hemozoin to prevent free heme toxicity. The parasite can also synthesize heme de novo, and all the enzymes in the pathway are characterized. To study the role of the dual heme sources in malaria parasite growth and development, we knocked out the first enzyme, d-aminolevulinate synthase (ALAS), and the last enzyme, ferrochelatase (FC), in the heme-biosynthetic pathway of Plasmodium berghei (Pb). The wild-type and knockout (KO) parasites had similar intraerythrocytic growth patterns in mice. We carried out in vitro radiolabeling of heme in Pb-infected mouse reticulocytes and Plasmodium falciparum-infected human RBCs using 4-(14) C] aminolevulinic acid (ALA). We found that the parasites incorporated both host hemoglobin-heme and parasite-synthesized heme into hemozoin and mitochondrial cytochromes. The similar fates of the two heme sources suggest that they may serve as backup mechanisms to provide heme in the intraerythrocytic stages. Nevertheless, the de novo pathway is absolutely essential for parasite development in the mosquito and liver stages. PbKO parasites formed drastically reduced oocysts and did not form sporozoites in the salivary glands. Oocyst production in PbALASKO parasites recovered when mosquitoes received an ALA supplement. PbALASKO sporozoites could infect mice only when the mice received an ALA supplement. Our results indicate the potential for new therapeutic interventions targeting the heme-biosynthetic pathway in the parasite during the mosquito and liver stages.

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Objective: The present study was undertaken to evaluate the antitumor and antioxidant status of ethanol extract of Terminalia catappa leaves against Ehrlich ascites carcinoma (EAC) in Swiss albino mice. Materials and Methods: The leaves powder was extracted with Soxhlet apparatus and subjected to hot continuous percolation using ethanol (95% v/v). Tumor bearing animals was treated with 50 and 200 mg/kg of ethanol extract. EAC induced in mice by intraperitoneal injection of EAC cells 1 x 10(6) cells/mice. The study was assed using life span of EAC-bearing hosts, hematological parameters, volume of solid tumor mass and status of antioxidant enzymes such as lipid peroxidation (LPO), reduced glutathione (GSH), superoxide dismutase (SOD) and catalase (CAT) activities. Total phenolics and flavonoids contents from the leaves extract were also determined. Results: Total phenolics and flavonoids contents from the leaves extract were found 354.02 and 51.67 mg/g extract. Oral administration of ethanol extract of T. catappa (50 and 200 mg/kg) increased the life span (27.82% and 60.59%), increased peritoneal cell count (8.85 +/- 0.20 and 10.37 +/- 0.26) and significantly decreased solid tumor mass (1.16 +/- 0.14 cm(2)) at 200 mg/kg as compared with EAC-tumor bearing mice (P < 0.01). Hematological profile including red blood cell count, white blood cell count, hemoglobin (11.91 +/- 0.47 % g) and protein estimation were found to be nearly normal levels in extract-treated mice compared with tumor bearing control mice. Treatment with T. catappa significantly decreased levels of LPO and GSH, and increased levels of SOD and CAT activity (P < 0.01). Conclusion: T. catappa exhibited antitumor effect by modulating LPO and augmenting antioxidant defense systems in EAC bearing mice. The phenolic and flavonoid components in this extract may be responsible for antitumor activity.

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Pore-forming toxins are known for their ability to efficiently form transmembrane pores which eventually leads to cell lysis. The dynamics of lysis and underlying self-assembly or oligomerization pathways leading to pore formation are incompletely understood. In this manuscript the pore-forming kinetics and lysis dynamics of Cytolysin-A (ClyA) toxins on red blood cells (RBCs) are quantified and compared with experimental lysis data. Lysis experiments are carried out on a fixed mass of RBCs, under isotonic conditions in phosphate-buffered saline, for different initial toxin concentrations ranging from 2.94-14.7 nM. Kinetic models which account for monomer binding, conformation and oligomerization to form the dodecameric ClyA pore complex are developed and lysis is assumed to occur when the number of pores per RBC (n(p)) exceeds a critical number, n(pc). By analysing the model in a sublytic regime (n(p) < n(pc)) the number of pores per RBC to initiate lysis is found to lie between 392 and 768 for the sequential oligomerization mechanism and between 5300 and 6300 for the non-sequential mechanism. Rupture rates which are first order in the number of RBCs are seen to provide the best agreement with the lysis experiments. The time constants for pore formation are estimated to lie between 1 and 20 s and monomer conformation time scales were found to be 2-4 times greater than the oligomerization times. Cell rupture takes places in 100s of seconds, and occurs predominantly with a steady number of pores ranging from 515 to 11 000 on the RBC surface for the sequential mechanism. Both the sequential irreversible and non-sequential kinetics provide similar predictions of the hemoglobin release dynamics, however the hemoglobin released as a function of the toxin concentration was accurately captured only with the sequential model. Each mechanism develops a distinct distribution of mers on the surface, providing a unique experimentally observable fingerprint to identify the underlying oligomerization pathways. Our study offers a method to quantify the extent and dynamics of lysis which is an important aspect of developing novel drug and gene delivery strategies based on pore-forming toxins.

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The temperature dependent electrical properties of the dropcasted Cu2SnS3 films have been measured in the temperature range 140 K to 317 K. The log I versus root V plot shows two regions. The region at lower bias is due to electrode limited Schottky emission and the higher bias region is due to bulk limited Poole Frenkel emission. The ideality factor is calculated from the ln I versus V plot for different temperatures fitted with the thermionic emission model and is found to vary from 6.05 eV to 12.23 eV. This large value is attributed to the presence of defects or amorphous layer at the Ag / Cu2SnS3 interface. From the Richardson's plot the Richardson's constant and the barrier height were calculated. Owing to the inhomogeneity in the barrier heights, the Richardson's constant and the barrier height were also calculated from the modified Richardson's plot. The I-V-T curves were also fitted using the thermionic field emission model. The barrier heights were found to be higher than those calculated using thermionic emission model. From the fit of the I-V-T curves to the field emission model, field emission was seen to dominate in the low temperature range of 140 K to 177 K. The temperature dependent current graphs show two regions of different mechanisms. The log I versus 1000/T plot gives activation energies E-a1 = 0.367095 - 0.257682 eV and E-a2 = 0.038416 - 0.042452 eV. The log ( I/T-2) versus 1000/T graph gives trap depths Phi(o1) = 0.314159 - 0.204752 eV and Phi(o2) = 0.007425- 0.011163 eV. With increasing voltage the activation energy E-a1 and the trap depth Phi(o1) decrease. From the ln (IT1/ 2) versus 1/T-1/ 4 graph, the low temperature region is due to variable range hopping mechanism and the high temperature region is due to thermionic emission. (C) 2014 Author(s).

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A variety of methods are available to estimate future solar radiation (SR) scenarios at spatial scales that are appropriate for local climate change impact assessment. However, there are no clear guidelines available in the literature to decide which methodologies are most suitable for different applications. Three methodologies to guide the estimation of SR are discussed in this study, namely: Case 1: SR is measured, Case 2: SR is measured but sparse and Case 3: SR is not measured. In Case 1, future SR scenarios are derived using several downscaling methodologies that transfer the simulated large-scale information of global climate models to a local scale ( measurements). In Case 2, the SR was first estimated at the local scale for a longer time period using sparse measured records, and then future scenarios were derived using several downscaling methodologies. In Case 3: the SR was first estimated at a regional scale for a longer time period using complete or sparse measured records of SR from which SR at the local scale was estimated. Finally, the future scenarios were derived using several downscaling methodologies. The lack of observed SR data, especially in developing countries, has hindered various climate change impact studies. Hence, this was further elaborated by applying the Case 3 methodology to a semi-arid Malaprabha reservoir catchment in southern India. A support vector machine was used in downscaling SR. Future monthly scenarios of SR were estimated from simulations of third-generation Canadian General Circulation Model (CGCM3) for various SRES emission scenarios (A1B, A2, B1, and COMMIT). Results indicated a projected decrease of 0.4 to 12.2 W m(-2) yr(-1) in SR during the period 2001-2100 across the 4 scenarios. SR was calculated using the modified Hargreaves method. The decreasing trends for the future were in agreement with the simulations of SR from the CGCM3 model directly obtained for the 4 scenarios.

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Climate change impact assessment studies involve downscaling large-scale atmospheric predictor variables (LSAPVs) simulated by general circulation models (GCMs) to site-scale meteorological variables. This article presents a least-square support vector machine (LS-SVM)-based methodology for multi-site downscaling of maximum and minimum daily temperature series. The methodology involves (1) delineation of sites in the study area into clusters based on correlation structure of predictands, (2) downscaling LSAPVs to monthly time series of predictands at a representative site identified in each of the clusters, (3) translation of the downscaled information in each cluster from the representative site to that at other sites using LS-SVM inter-site regression relationships, and (4) disaggregation of the information at each site from monthly to daily time scale using k-nearest neighbour disaggregation methodology. Effectiveness of the methodology is demonstrated by application to data pertaining to four sites in the catchment of Beas river basin, India. Simulations of Canadian coupled global climate model (CGCM3.1/T63) for four IPCC SRES scenarios namely A1B, A2, B1 and COMMIT were downscaled to future projections of the predictands in the study area. Comparison of results with those based on recently proposed multivariate multiple linear regression (MMLR) based downscaling method and multi-site multivariate statistical downscaling (MMSD) method indicate that the proposed method is promising and it can be considered as a feasible choice in statistical downscaling studies. The performance of the method in downscaling daily minimum temperature was found to be better when compared with that in downscaling daily maximum temperature. Results indicate an increase in annual average maximum and minimum temperatures at all the sites for A1B, A2 and B1 scenarios. The projected increment is high for A2 scenario, and it is followed by that for A1B, B1 and COMMIT scenarios. Projections, in general, indicated an increase in mean monthly maximum and minimum temperatures during January to February and October to December.

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Mrhl RNA is a nuclear lncRNA encoded in the mouse genome and negatively regulates Wnt signaling in spermatogonial cells through p68/Ddx5 RNA helicase. Mrhl RNA is present in the chromatin fraction of mouse spermatogonial Gc1-Spg cells and genome wide chromatin occupancy of mrhl RNA by ChOP (Chromatin oligo affinity precipitation) technique identified 1370 statistically significant genomic loci. Among these, genes at 37 genomic loci also showed altered expression pattern upon mrhl RNA down regulation which are referred to as GRPAM (Genes Regulated by Physical Association of Mrhl RNA). p68 interacted with mrhl RNA in chromatin at these GRPAM loci. p68 silencing drastically reduced mrhl RNA occupancy at 27 GRPAM loci and also perturbed the expression of GRPAM suggesting a role for p68 mediated mrhl RNA occupancy in regulating GRPAM expression. Wnt3a ligand treatment of Gc1-Spg cells down regulated mrhl RNA expression and also perturbed expression of these 27 GRPAM genes that included genes regulating Wnt signaling pathway and spermatogenesis, one of them being Sox8, a developmentally important transcription factor. We also identified interacting proteins of mrhl RNA associated chromatin fraction which included Pc4, a chromatin organizer protein and hnRNP A/B and hnRNP A2/B1 which have been shown to be associated with lincRNA-Cox2 function in gene regulation. Our findings in the Gc1-Spg cell line also correlate with the results from analysis of mouse testicular tissue which further highlights the in vivo physiological significance of mrhl RNA in the context of gene regulation during mammalian spermatogenesis.

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This paper reports the structure, microstructure and magnetic properties of Fe-Ga thin films deposited using DC magnetron sputtering technique on Si(100) substrate kept at different temperatures. Structural studies employing X-ray diffraction and TEM revealed the presence of only disordered A2 phase in the film. Columnar growth of nanocrystalline grains from the substrate was observed in the film deposited at room temperature. With increase in substrate temperature the grain size as well as surface roughness was found to increase. The magnetization of the films deposited at higher substrate temperatures were Found to saturate at lower magnetic held as compared to the room temperature deposited Film. Coercivity was found to decrease with increasing substrate temperature upto a minimum value of similar to 2 Oe for the film deposited at 450 degrees C and with further increase in substrate temperature it was found to increase. A maximum magnetostriction of 200 mu-strains was also observed for the film deposited at 450 degrees C. (C) 2015 Elsevier B.V. All rights reserved

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Glycated hemoglobin (HbA(1c)) is a `gold standard' biomarker for assessing the glycemic index of an individual. HbA(1c) is formed due to nonenzymatic glycosylation at N-terminal valine residue of the P-globin chain. Cation exchange based high performance liquid chromatography (CE HPLC) is mostly used to quantify HbA(1c), in blood sample. A few genetic variants of hemoglobin and post-translationally modified variants of hemoglobin interfere with CE HPLC-based quantification,. resulting in its false positive estimation. Using mass spectrometry, we analyzed a blood sample with abnormally high HbA(1c) (52.1%) in the CE HPLC method. The observed HbA(1c) did not corroborate the blood glucose level of the patient. A mass spectrometry based bottom up proteomics approach, intact globin chain mass analysis, and chemical modification of the proteolytic peptides identified the presence of Hb Beckman, a genetic variant of hemoglobin, in the experimental sample. A similar surface area to charge ratio between HbA(1c) and Hb Beckman might have resulted in the coelution of the variant with HbA(1c) in CE HPLC. Therefore, in the screening of diabetes mellitus through the estimation of HbA(1c), it is important to look for genetic variants of hemoglobin in samples that show abnormally high glycemic index, and HbA(1c) must be estimated using an alternative method. (C) 2015 Elsevier Inc. All rights reserved.

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Digestion of food in the intestines converts the compacted storage carbohydrates, starch and glycogen, to glucose. After each meal, a flux of glucose (>200 g) passes through the blood pool (4-6 g) in a short period of 2 h, keeping its concentration ideally in the range of 80-120 mg/100 mL. Tissue-specific glucose transporters (GLUTs) aid in the distribution of glucose to all tissues. The balance glucose after meeting the immediate energy needs is converted into glycogen and stored in liver (up to 100 g) and skeletal muscle (up to 300 g) for later use. High blood glucose gives the signal for increased release of insulin from pancreas. Insulin binds to insulin receptor on the plasma membrane and activates its autophosphorylation. This initiates the post-insulin-receptor signal cascade that accelerates synthesis of glycogen and triglyceride. Parallel control by phos-dephos and redox regulation of proteins exists for some of these steps. A major action of insulin is to inhibit gluconeogensis in the liver decreasing glucose output into blood. Cases with failed control of blood glucose have alarmingly increased since 1960 coinciding with changed life-styles and large scale food processing. Many of these turned out to be resistant to insulin, usually accompanied by dysfunctional glycogen storage. Glucose has an extended stay in blood at 8 mM and above and then indiscriminately adds on to surface protein-amino groups. Fructose in common sugar is 10-fold more active. This random glycation process interferes with the functions of many proteins (e.g., hemoglobin, eye lens proteins) and causes progressive damage to heart, kidneys, eyes and nerves. Some compounds are known to act as insulin mimics. Vanadium-peroxide complexes act at post-receptor level but are toxic. The fungus-derived 2,5-dihydroxybenzoquinone derivative is the first one known to act on the insulin receptor. The safe herbal products in use for centuries for glucose control have multiple active principles and targets. Some are effective in slowing formation of glucose in intestines by inhibiting alpha-glucosidases (e.g., salacia/saptarangi). Knowledge gained from French lilac on active guanidine group helped developing Metformin (1,1-dimethylbiguanide) one of the popular drugs in use. One strategy of keeping sugar content in diets in check is to use artificial sweeteners with no calories, no glucose or fructose and no effect on blood glucose (e.g., steviol, erythrytol). However, the three commonly used non-caloric artificial sweetener's, saccharin, sucralose and aspartame later developed glucose intolerance, the very condition they are expected to evade. Ideal way of keeping blood glucose under 6 mM and HbAlc, the glycation marker of hemoglobin, under 7% in blood is to correct the defects in signals that allow glucose flow into glycogen, still a difficult task with drugs and diets.

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Standard or 'traditional' human insulin preparations such as regular soluble insulin and neutral protamine Hagedorn (NPH) insulin have shortcomings in terms of their pharmacokinetic and pharmacodynamic properties that limit their clinical efficacy. Structurally modified insulin molecules or insulin 'analogs' have been developed with the aim of delivering insulin replacement therapy in a more physiological manner. In the last 10 years, five insulin analog preparations have become commercially available for clinical use in patients with type 1 diabetes mellitus: three 'rapid' or fast-acting analogs (insulin lispro, aspart, and glulisine) and two long-acting analogs (insulin glargine and detemir). This review highlights the specific pharmacokinetic properties of these new insulin analog preparations and focuses on their potential clinical advantages and disadvantages when used in children and adolescents with type 1 diabetes mellitus. The fast-acting analogs specifically facilitate more flexible insulin injection timing with regard to meals and activities, whereas the long-acting analogs have a more predictable profile of action and lack a peak effect. To date, clinical trials in children and adolescents have been few in number, but the evidence available from these and from other studies carried out in adults with type 1 diabetes suggest that they offer significant benefits in terms of reduced frequency of nocturnal hypoglycemia, better postprandial blood glucose control, and improved quality of life when compared with traditional insulins. In addition, insulin detemir therapy is unique in that patients may benefit from reduced risk of excessive weight, particularly during adolescence. Evidence for sustained long-term improvements in glycosylated hemoglobin, on the other hand, is modest. Furthermore, alterations to insulin/insulin-like growth factor I receptor binding characteristics have also raised theoretical concerns that insulin analogs may have an increased mitogenic potential and risk of tumor development, although evidence from both in vitro and in vivo animal studies do not support this assertion. Long-term surveillance has been recommended and further carefully designed prospective studies are needed to evaluate the overall benefits and clinical efficacy of insulin analog therapy in children and adolescents with type 1 diabetes.

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Se realizó un estudio de rotación de cultivos y métodos de control de malezas en el cultivo de soya, en terrenos del Instituto "Rigoberto López Pérez" de Managua, sobre un suelo de textura franco - arcillosa. La siembra se realizó el 26 de Agosto de 1989, utilizando un diseño de parcelas divididas en bloques completamente al azar, siendo el factor "A": Cultivos antecedentes; al= maíz, a2= pepinillo; y el factor "B": Métodos de control de malezas; b1= fomesafén (0.351 l/ha) en post-emergencia; b2= limpia en período crítico y b3= limpias periódicas. Este experimento se realizó con el objetivo de estudiar el efecto de estos factores sobre la dinámica de las malezas y el crecimiento, desarrollo y rendimiento de la soya. Los resultados reflejan que el cultivo antecedente maíz representa la menor abundancia, cobertura y biomasa de malezas al momento de la cosecha siendo la especie más abundante Cenchrus brownii y el cultivo antecedente pepinillo la menor diversidad con mayor abundancia de la especie Sida acuta. El efecto de este factor sobre el crecimiento, desarrollo y rendimiento de la soya indica que se obtuvieron diferencias significativas solamente para el peso de 1000 semillas con 135.59 g (gramos) a favor del cultivo antecedente maíz; además se obtiene el mayor número de ramas por planta, rendimiento y peso seco de la paja con 1615.65 y 5266.67 kg/ha respectivamente. Las otras variables registran un comportamiento similar. En cuanto al efecto de loe métodos de control de malezas; la menor abundancia, cobertura y biomasa de las malezas se presentó en el método con limpia periódica y el mayor valor cuando se aplicó fomesafén en post-emergencia siendo para este caso la especie más abundante Sida acota. La diversidad fue similar al momento de la cosecha donde la especie C.brownii se ve favorecida por las limpias periódicas, no obstante las variables de crecimiento, desarrollo y rendimiento de la soya se presentaron diferencias significativas únicamente para el peso de 1000 semillas obteniéndose 139.26 g a favor de las limpias en período crítico, además se obtiene el mayor número de ramas por planta; pero se presenta el menor número de vaina por planta y peso seco de la paja con 4750 kg/ha. Por otro lado, el mayor rendimiento se obtuvo cuando se aplicó fomesafén en post-emergencia y el menor cuando se utilizaron limpias periódicas con valores de 1547.88 y 1462.15 kg/ha respectivamente. Con fomesafén se presentó además la menor población y número de vainas por planta y con limpias periódicas el menor peso de 1000 semillas con 122,93 g, el menor rendimiento con 1462.15 kg/ha, pero presentó el mayor peso seco de paja con 5025 kg/ha.

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En el presente estudio se evaluó la influencia de rotaciones de cultivo y métodos de control de malezas, sobre la cenosis de malezas, y el crecimiento y rendimiento de frijol común. El ensayo se realizó en la época de primera con el establecimiento de los cultivos antecesores (mayo - agosto, 1994), y se continuo durante la postrera con el cultivo principal (septiembre - diciembre, 1994), en la estación experimental La Compañía, ubicada en el municipio de San Marcos, Carazo. Se utilizó un diseño de parcelas divididas, arreglados en bloques completos al azar, con cuatro repeticiones. El factor A, estuvo constituido por las rotaciones: al: maíz - frijol, a2: sorgo - frijol, a3: frijol - frijol y a4: malezas - frijol. En el factor B, se incluyeron los controles de malezas: bl: control con cobertura de maíz, b2: control mecánico (azadón a los 21 días después de la siembra) y b3: control químico (fluazifop-butyl más fomesafen en dósis de 1.421/ha de cada uno de los herbicidas). Los resultados muestran que las rotaciones de cultivo tuvieron influencia sobre los niveles de enmalezamiento, siendo más efectiva la rotación maíz-frijol y sorgo frijol en reducir la abundancia y la acumulación de peso seco. Los rendimientos de grano fueron superiores en la rotación malezas-frijol, en cambio la rotación frijol - frijol obtuvo rendimiento bajo debido principalmente a la alta incidencia y severidad de mustia hilachosa (Thanatephorus cucumeris (Frank) Donk). La mejor rentabilidad la presentó la rotación malezas-frijol. En referencia a los controles de malezas, el control químico efectuó un control satisfactorio de las malezas, mientras que los controles cobertura de maíz y mecánico fueron insuficientes por la predominancia de malezas de hoja ancha contra las cuales no existe especificidad de dichos controles. A pesar de lo anterior la mejor rentabilidad se obtuvo en el control mecánico, ya que alcanzó buenos rendimientos y los costos de control de malezas son inferiores al control químico.

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En el presente estudio se evaluó la influencia de rotaciones de cultivo y métodos de control de malezas, sobre la dinámica de las malezas y el crecimiento y rendimiento de frijol común. El ensayo se realizó en la época de primera con el establecimiento de los cultivos antecesores: maíz, sorgo, frijol y malezas (mayo-agosto, 1996} y se continuó durante la postrera con el cultivo principal (septiembre-diciembre, 1996) en la estación experimental La Compañía, ubicada en el municipio de San Marcos, Carazo. Se estableció un experimento factorial con diseño en Bloques Completos al Azar (BCA) con arreglos en parcelas divididas con cuatro repeticiones. El factor A, estuvo constituido por las rotaciones: al: maíz-frijol, a2: sorgo-frijol, a3:frijol­ frijol, a4: malezas-frijol. En el factor B, se incluyeron los controles de malezas:bl: control con cobertura de maíz, b2: control mecánico (azadón a los 21 días después de la siembra) y b3: control químico ( tluazitop-butyl más fomesafen en dosis equivalentes 1.42 1/ha de cada uno de los herbicidas). Los resultados muestran que las rotaciones de cultivo tuvieron influencia sobre tos niveles de enmalezamiento, siendo más efectiva la rotación sorgo-frijol y maíz-frijol en reducir la abundancia de malezas. La menor acumulación de peso seco en malezas lo presentó la rotación frijol-frijol. Los rendimientos de grano fueron superiores en la rotación frijol-frijol. En referencia a los controles de malezas, el mejor efecto sobre las malezas y el mejor rendimiento se obtuvo con el control químico, mientras el control con cobertura fue insuficiente para el manejo de malezas. La mejor rentabilidad se obtuvo con el control químico por los buenos rendimientos obtenidos, ya que permiten la compensación de los costos, que estos son superiores con respecto a tos otros controles. El análisis económico realizado a las rotaciones de cultivo indica que el tratamiento con mayor rentabilidad fue la rotación con frijol y la de menor rentabilidad la rotación con maleza, en cuanto a los controles de malezas el tratamiento de mayor rentabilidad fue el control químico.

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Durante la época de primera de 1994, se estableció un experimento de campo en la estación experimental La Compañia, localizada en el municipio de San Marcos, Carazo, con el propósito de evaluar la influencia de dos sistemas de labranza y tres métodos de control de malezas sobre la dinámica de las malezas, el crecimiento y rendimiento del cultivo de maíz (Zea mays L.). Se utilizó un diseño de parcelas divididas, arreglados en bloques completos al azar la parcela grande correspondió a las labranzas y las pequeñas a los controles, con cuatro repeticiones. Los factores en estudio fueron A:sistema de labranza, con los siguientes niveles al: labranza cero y a2: mínima y B: Control de malezas con los siguientes niveles: b1: control de malezas pre emergente (utilizando paraquat), b2: pre emergente más chapia a los 28 dias después de la siembra, y b3: aplicación pre emergente más post emergente, con la utilización de paraquat a la siembra y a los 28 días después de la siembra. Los resultados indican que la labranza cero, mostró efectos negativos sobre la dinámica de las malezas, sobre todo en cuanto a dominancia y diversidad, no asi en abundancia donde ambos sistemas mostraron similitud. El mejor método de control de malezas fue pre emergente más post emergente, seguido de pre emergente má chapia y el menos efectivo fue el control pre emergente. En las variables de crecimiento, tanto los sistemas de labranzas como de los metodos de control de malezas, no mostraron efectos significativos. La evaluación de los componentes del rendimiento en los sistemas de labranzas no mostraron diferencias significativas, no obstante labranza cero mostró mejores resultados en longitud de mazorca, con un valor de 9.47 cm, número de granos por hilera 20, peso de cien granos 18.5gr. y rendimiento de grano 1681.3kg/ha. Los métodos de control de malezas mostraron pocas diferencias significativas en los componentes del rendimiento. El control pre emergente más pos emergente mostró los mejores resultados en diámetro de mazorca con un valor de 4.02cm., número de hileras por mazorca 13.25, número de granos por hilera 21.25, rendimiento 1881.2kg/ha y peso de paja 1972.4kg/. Existieron diferencias significativas en el rendimiento de grano en los controles de malezas, el mejor comportamiento lo presentó el control pre emergente más post emergente. La mejor rentabilidad la obtuvieron el sistema de labranza cero y el control de malezas pre emergente más post emergente, debido a que estos ofrecen mayores beneficios netos, además obtuvieron loa mejores rendimientos.