Disponibilidade biológica do fósforo de diferentes fontes para eqüinos em crescimento

Objetivou-se neste estudo, determinar a disponibilidade biológica do P de diferentes fontes, para eqüinos em fase de crescimento. Utilizaram-se dezesseis eqüinos machos em fase de crescimento, submetidos à aplicação de quatro fontes fosfatadas -- fosfato de rocha de Tapira (TAP), fosfato de rocha de Patos de Minas (PAT), fosfato bicálcico (BIC) e farinha de osso (FOS) --, adicionadas à dieta basal em quantidades suficientes para fornecer 22 g de P/animal/dia. No 16º dia, foram-lhes injetados 30 MBq de 32P/animal, e coletaram-se amostras de sangue, fezes e urina, durante sete dias. Foram determinadas as atividades específicas no plasma, fezes e urina e calculou-se a perda endógena fecal e a absorção real de P. Os valores obtidos quanto ao P consumido, P excretado, P no plasma e P retido não apresentaram diferenças estatísticas (P>0,05). Os valores de absorção real do P do TAP, PAT, BIC e da FOS foram, respectivamente, 25,23%, 33,97%, 31,71% e 29,36%. Não houve diferenças estatísticas (P>0,05) entre as fontes estudadas. Em relação ao BIC, as rochas fosfáticas apresentaram altos valores de disponibilidade biológica.

Danos ao DNA promovidos por ácido 5-aminolevulínico: possível associação com o desenvolvimento de carcinoma hepatocelular em portadores de porfiria aguda intermitente

5-Aminolevulinic acid (ALA) is a heme precursor accumulated in acute intermittent porphyria (AIP), which might be associated with hepatocellular carcinoma (HCC) in symptomatic patients. Under metal catalyzed oxidation, ALA and its cyclic dimerization product, 3,6-dihydropyrazine-2,5-dipropanoic acid, produce reactive oxygen species that damage plasmid and calf thymus DNA bases, increase the steady state level of 8-oxo-7,8-dihydro-2´-deoxyguanosine in liver DNA and promote mitochondrial DNA damage. The final product of ALA, 4,5-dioxovaleric acid (DOVA), is able to alkylate guanine moieties, producing adducts. ALA and DOVA are mutagenic in bacteria. This review shows an up-to-date literature data that reinforce the hypothesis that the DNA damage induced by ALA may be associated with the development of HCC in AIP patients.

Relação entre resistência de linhagens tropicais de milho à podridão de espiga e ao acúmulo de fumonisinas provocados por Fusarium verticillioides

A infecção de grãos de milho por Fusarium verticillioides, agente causal da podridão da espiga, pode resultar na produção de micotoxinas do grupo das fumonisinas. A resistência genética é a forma de controle mais eficiente dessa enfermidade. Assim, o objetivo do trabalho foi buscar fontes de resistência em linhagens de milho tropical à F. verticillioides e à produção de fumonisinas. Seis linhagens tropicais de milho, três, pré-classificadas como resistentes e três, pré-classificadas como suscetíveis à F. verticillioides, foram submetidas à inoculação do patógeno e posteriormente, avaliadas quanto à severidade da podridão de espiga, incidência de grãos sintomáticos e concentração de fumonisinas. Os resultados mostraram que as linhagens R1 e R3 apresentaram alta resistência à infecção do patógeno. No entanto, apenas a R3 foi resistente ao acúmulo de fumonisinas. Dessa forma, sugere-se que a ausência de relação entre intensidade da doença e níveis de fumonisinas seja fator inerente desse patossistema. Assim, não é possível assegurar que grãos assintomáticos quanto à infecção por F. verticillioides, estejam livres de contaminação por fumonisinas.

Reação de cultivares de tangerineira à antracnose sob diferentes sistemas de irrigação

A tangerineira é uma das espécies de Citrus mais importantes, comercialmente. No entanto, é elevada a quantidade de patógenos que afetam a cultura, destacando-se o fungo Colletotrichum gloeosporioides, causador da antracnose. A antracnose pode resultar em grandes prejuízos econômicos, ocasionando perdas de produção e qualidade dos frutos. O objetivo deste trabalho foi avaliar a resistência de cultivares de tangerineira à antracnose em diferentes sistemas de irrigação. Foi estudada a incidência da antracnose em três cultivares de tangerineira, sob três sistemas de cultivo. Utilizaram-se as cultivares 'Murcote', 'Ponkan' e 'Cravo', enxertadas sobre porta-enxerto de limão Cravo e os sistemas de irrigação por microaspersão e por gotejamento. Uma testemunha de sequeiro foi incluída. Os resultados mostraram que as plantas cultivadas sob irrigação são mais resistentes à antracnose que aquelas sob regime de sequeiro, sendo que a cultivar Ponkan apresentou maior resistência genética á antracnose. Verificou-se também que existe correlação positiva entre a incidência baseada no percentual de plantas afetadas e a incidência com base no número de ramos afetados por planta.

Caracterização histológica e imuno-histoquímica das lesões de tuberculose em bovinos e de linfadenite granulomatosa em suínos

Mycobacterium sp. induz inflama&#231;&#227;o granuloma-tosa em diferentes esp&#233;cies animais. Mycobacterium bovis e o complexo Mycobacterium avium s&#227;o importantes pat&#243;genos de bovinos e su&#237;nos e podem causar infec&#231;&#227;o em humanos, principalmente imunossuprimidos. Perdas na produ&#231;&#227;o, barreiras comerciais e preju&#237;zos por condena&#231;&#227;o de carca&#231;as em abatedouro/frigor&#237;fico est&#227;o atrelados &#224; ocorr&#234;ncia dessas infec&#231;&#245;es, com preju&#237;zos econ&#244;micos significativos. Foi realizado um estudo de casos diagnosticados como tuberculose em bovinos e linfadenite granulomatosa em su&#237;nos no Setor de Patologia Veterin&#225;ria da Universidade Federal do Rio Grande do Sul (SPV-UFRGS) no per&#237;odo de janeiro de 2007 a dezembro de 2011. Dados referentes &#224; ra&#231;a, ao sexo, &#224; idade e ao hist&#243;rico cl&#237;nico foram compilados dos livros de registro e analisados. As caracter&#237;sticas histol&#243;gicas das les&#245;es em linfonodos e pulm&#245;es foram avaliadas em Hematoxilina-Eosina, com predom&#237;nio de c&#233;lulas gigantes nas les&#245;es de tuberculose bovina e de macr&#243;fagos epitelioides em su&#237;nos. As t&#233;cnicas histoqu&#237;micas de Ziehl-Neelsen e Tricr&#244;mico de Masson foram utilizadas para evidenciar, respectivamente, bacilos &#225;lcool-&#225;cido resistentes e tecido conjuntivo fibroso nas les&#245;es. A t&#233;cnica de imuno-histoqu&#237;mica foi utilizada em aproximadamente 30% dos casos estudados de cada esp&#233;cie, selecionados aleatoriamente, para a caracteriza&#231;&#227;o do infiltrado linfoc&#237;tico. Foram utilizados os anticorpos anti-CD3 para a marca&#231;&#227;o de linf&#243;citos T e anti-CD79&#945;cy para a marca&#231;&#227;o de linf&#243;citos B. Linf&#243;citos T predominaram nas les&#245;es em ambas as esp&#233;cies, com diferen&#231;a estatisticamente significativa entre as m&#233;dias dos linf&#243;citos T e linf&#243;citos B. Foi usado o teste t pareado, com t=5,501 (p<0,001) nas les&#245;es dos bovinos e t=5,826 (p<0,001) para as les&#245;es de linfadenite dos su&#237;nos. Adicionalmente foram marcados macr&#243;fagos com o uso do anticorpo anti-CD68 para bovinos e anti-Lisozima para su&#237;nos. Al&#233;m desses, o anticorpo policlonal anti-Mycobacterium tuberculosis foi utilizado para a detec&#231;&#227;o de bact&#233;rias do g&#234;nero Mycobacterium, com imunomarca&#231;&#227;o positiva em todos os casos e, nos casos dos su&#237;nos, houve marca&#231;&#227;o anti-Mycobacterium avium.

Competição de azevém (Lolium multiflorum L. ) com duas cultivares de trigo

Com os objetivos de avaliar a habilidade de duas cultivares de trigo em competir com azevém (Lolium multiflorum, L.) e de estimar os efeitos da concorrência de várias densidades desta espécie sobre a cultura, foi conduzido experimento a campo durante a estação de crescimento de 1978, na Estação Experimental Agronõmica da UFRGS, em Guaíba, RS. Foram comparadas as cultivares de trigo 'E-7414' e 'PAT-7219', na população de 300 plantas por m', com azevém semeado nas densidades de 0, 2,5, 5,0, 10,0 e 20,0 kg/ha, as quais originaram populações médias de 0, 130, 210, 470 e 750 plantas por m² , respectivamente. A competição entre as espécies foi mantida durante o ciclo da cultura. Para o rendimento de grãos da cultivar 'E-7414', a competição exercida pelo azevém ocasionou decréscimos variáveis entre 18% e 56%, dependendo da infestação; enquanto para a cultivar 'PAT-7219', as reduções no rendimento de grãos se situaram entre 4c é 22%, conforme a densidade do azevém. Enquanto para 'PAT-7219' não foram significativas as reduções no rendimento de grãos, para `E-7414' os decréscimos verificados alcançaram significância estatística. A análise do peso da matéria seca do azevém demonstrou que este aumentou proporcionalmente ao aumento de sua população, mas que aquela variável foi significativamente menor quando o azevém esteve competindo com 'PAT-7219' do que com `E-7414'. Em média, diminuiu em 31% a matéria seca do azevém produzida sob 'PAT-7219' em relação à `E-7414'.

Poliporóides (Basidiomycota) em fragmentos de mata no perímetro urbano de São José do Rio Preto, São Paulo, Brasil

Foi realizado levantamento das espécies de fungos poliporóides que ocorrem no perímetro urbano do município de São José do Rio Preto (20º49'12" S, 49º22'44" W), Estado de São Paulo, Brasil. Foram identificadas 18 espécies pertencentes a 11 gêneros de Agaricales (Schizophyllaceae), Hymenochaetales (Hymenochaetaceae) e Polyporales (Ganodermataceae, Gloeophyllaceae, Meruliaceae e Polyporaceae): Coriolopsis floccosa (Jungh.) Ryvarden, C. polyzona (Pers.) Ryvarden, Datronia caperata (Berk.) Ryvarden, D. mollis (Somf.:Fr.) Donk., Ganoderma australe (Fr.) Pat., Gloeophyllum striatum (Sw.) Murrill, Gloeoporus thelephoroides (Hook.) G. Cunn., Hexagonia hirta (P. Beauv.) Fr., H. hydnoides (Sw.) M. Fidalgo, H. papyracea Berk., Polyporus tenuiculus (P. Beauv.) Fr., Phellinus callimorphus (Lév.) Ryvarden, P. gilvus (Schwein.) Pat., P. umbrinellus (Bres.) Herrera &amp; Bondartseva, Pycnoporus sanguineus (L.) Murrill, Schizophyllum commune Fr., S. umbrinum Berk. e Trametes modesta (Kunze:Fr.) Ryvarden. Datronia mollis é nova citação para o Estado de São Paulo. São apresentados chave de identificação, descrições e comentários para cada táxon estudado.

Low occurrence of occult hepatitis B virus infection and high frequency of hepatitis C virus genotype 3 in hepatocellular carcinoma in Brazil

Occult hepatitis B virus (HBV) infection has been reported among patients with hepatitis C virus (HCV) infection and hepatocellular carcinoma (HCC). Our aim was to evaluate the presence of occult HBV infection in patients with HCV-related liver cirrhosis (LC) with or without HCC in São Paulo, Brazil. Serum and liver tissue samples from 50 hepatitis B surface antigen-negative patients with HCV-related LC who underwent liver transplantation at the University of São Paulo School of Medicine Hospital from 1993 to 2004 were divided into groups with LC only (N = 33) and with LC plus HCC (N = 17). HBV DNA was assayed for serum and paraffin-embedded liver tissue (tumoral and non-tumoral) using real time PCR and only 1 case with HCC had HBV DNA-positive serum. All liver samples were negative. HCV genotype 3 was detected in 17/39 (43.7%) cases. In conclusion, using a sensitive real time PCR directed to detect HBV variants circulating in Brazil, occult hepatitis B infection was not found among HCV-positive cirrhotic patients and was rarely found among HCV-positive HCC patients. These results are probably related to the low prevalence of HBV infection in our population. Furthermore, we have also shown that HCV genotype 3 is frequently found in Brazilian cirrhotic patients, particularly when they also have HCC. More studies involving a large number of cases should be carried out to confirm these data and to further characterize Brazilian HCV genotype isolates to elucidate genetic features that might be related to its carcinogenic potential.

Does hepatocellular carcinoma in non-alcoholic steatohepatitis exist in cirrhotic and non-cirrhotic patients?

Non-alcoholic steatohepatitis (NASH) has been associated with hepatocellular carcinoma (HCC) often arising in histologically advanced disease when steatohepatitis is not active (cryptogenic cirrhosis). Our objective was to characterize patients with HCC and active, histologically defined steatohepatitis. Among 394 patients with HCC detected by ultrasound imaging over 8 years and staged by the Barcelona Clinic Liver Cancer (BCLC) criteria, we identified 7 cases (1.7%) with HCC occurring in the setting of active biopsy-proven NASH. All were negative for other liver diseases such as hepatitis C, hepatitis B, autoimmune hepatitis, Wilson disease, and hemochromatosis. The patients (4 males and 3 females, age 63 ± 13 years) were either overweight (4) or obese (3); 57% were diabetic and 28.5% had dyslipidemia. Cirrhosis was present in 6 of 7 patients, but 1 patient had well-differentiated HCC in the setting of NASH without cirrhosis (fibrosis stage 1) based on repeated liver biopsies, the absence of portal hypertension by clinical and radiographic evaluations and by direct surgical inspection. Among the cirrhotic patients, 71.4% were clinically staged as Child A and 14.2% as Child B. Tumor size ranged from 1.0 to 5.2 cm and 5 of 7 patients were classified as early stage; 46% of all nodules were hyper-echoic and 57% were <3 cm. HCC was well differentiated in 1/6 and moderately differentiated in 5/6. Alpha-fetoprotein was <100 ng/mL in all patients. HCC in patients with active steatohepatitis is often multifocal, may precede clinically advanced disease and occurs without diagnostic levels of alpha-fetoprotein. Importantly, HCC may occur in NASH in the absence of cirrhosis. More aggressive screening of NASH patients may be warranted.

Differential gene expression profiles of hepatocellular carcinomas associated or not with viral infection

Chronic hepatitis B (HBV) and C (HCV) virus infections are the most important factors associated with hepatocellular carcinoma (HCC), but tumor prognosis remains poor due to the lack of diagnostic biomarkers. In order to identify novel diagnostic markers and therapeutic targets, the gene expression profile associated with viral and non-viral HCC was assessed in 9 tumor samples by oligo-microarrays. The differentially expressed genes were examined using a z-score and KEGG pathway for the search of ontological biological processes. We selected a non-redundant set of 15 genes with the lowest P value for clustering samples into three groups using the non-supervised algorithm k-means. Fisher&#8217;s linear discriminant analysis was then applied in an exhaustive search of trios of genes that could be used to build classifiers for class distinction. Different transcriptional levels of genes were identified in HCC of different etiologies and from different HCC samples. When comparing HBV-HCC vs HCV-HCC, HBV-HCC/HCV-HCC vs non-viral (NV)-HCC, HBC-HCC vs NV-HCC, and HCV-HCC vs NV-HCC of the 58 non-redundant differentially expressed genes, only 6 genes (IKBK&#946;, CREBBP, WNT10B, PRDX6, ITGAV, and IFNAR1) were found to be associated with hepatic carcinogenesis. By combining trios, classifiers could be generated, which correctly classified 100% of the samples. This expression profiling may provide a useful tool for research into the pathophysiology of HCC. A detailed understanding of how these distinct genes are involved in molecular pathways is of fundamental importance to the development of effective HCC chemoprevention and treatment.

BC047440 antisense eukaryotic expression vectors inhibited HepG2 cell proliferation and suppressed xenograft tumorigenicity

The biological functions of the BC047440 gene highly expressed by hepatocellular carcinoma (HCC) are unknown. The objective of this study was to reconstruct antisense eukaryotic expression vectors of the gene for inhibiting HepG2 cell proliferation and suppressing their xenograft tumorigenicity. The full-length BC047440 cDNA was cloned from human primary HCC by RT-PCR. BC047440 gene fragments were ligated with pMD18-T simple vectors and subsequent pcDNA3.1(+) plasmids to construct the recombinant antisense eukaryotic vector pcDNA3.1(+)BC047440AS. The endogenous BC047440 mRNA abundance in target gene-transfected, vector-transfected and naive HepG2 cells was semiquantitatively analyzed by RT-PCR and cell proliferation was measured by the MTT assay. Cell cycle distribution and apoptosis were profiled by flow cytometry. The in vivo xenograft experiment was performed on nude mice to examine the effects of antisense vector on tumorigenicity. BC047440 cDNA fragments were reversely inserted into pcDNA3.1(+) plasmids. The antisense vector significantly reduced the endogenous BC047440 mRNA abundance by 41% in HepG2 cells and inhibited their proliferation in vitro (P < 0.01). More cells were arrested by the antisense vector at the G1 phase in an apoptosis-independent manner (P = 0.014). Additionally, transfection with pcDNA3.1(+)BC047440AS significantly reduced the xenograft tumorigenicity in nude mice. As a novel cell cycle regulator associated with HCC, the BC047440 gene was involved in cell proliferation in vitro and xenograft tumorigenicity in vivo through apoptosis-independent mechanisms.

Retinoic acid and cAMP inhibit rat hepatocellular carcinoma cell proliferation and enhance cell differentiation

Hepatocellular carcinoma (HCC) is the third highest cause of cancer death worldwide. In general, the disease is diagnosed at an advanced stage when potentially curative therapies are no longer feasible. For this reason, it is very important to develop new therapeutic approaches. Retinoic acid (RA) is a natural derivative of vitamin A that regulates important biological processes including cell proliferation and differentiation. In vitro studies have shown that RA is effective in inhibiting growth of HCC cells; however, responsiveness to treatment varies among different HCC cell lines. The objective of the present study was to determine if the combined use of RA (0.1 µM) and cAMP (1 mM), an important second messenger, improves the responsiveness of HCC cells to RA treatment. We evaluated the proliferative behavior of an HCC cell line (HTC) and the expression profile of genes related to cancer signaling pathway (ERK and GSK-3&#946;) and liver differentiation (E-cadherin, connexin 26 (Cx26), and Cx32). RA and cAMP were effective in inhibiting the proliferation of HTC cells independently of combined use. However, when a mixture of RA and cAMP was used, the signals concerning the degree of cell differentiation were increased. As demonstrated by Western blot, the treatment increased E-cadherin, Cx26, Cx32 and Ser9-GSK-3&#946; (inactive form) expression while the expression of Cx43, Tyr216-GSK-3&#946; (active form) and phosphorylated ERK decreased. Furthermore, telomerase activity was inhibited along treatment. Taken together, the results showed that the combined use of RA and cAMP is more effective in inducing differentiation of HTC cells.

Association of MDR1 gene polymorphisms with the risk of hepatocellular carcinoma in the Chinese Han population

The multidrug resistance 1 gene (MDR1) is an important candidate gene for influencing susceptibility to hepatocellular carcinoma (HCC). The objective of the present study was to evaluate the association ofMDR1 polymorphisms with the risk of HCC in the Chinese Han population. A total of 353 HCC patients and 335 healthy subjects were enrolled in the study. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), created restriction site-PCR (CRS-PCR) and DNA sequencing methods were used to identify MDR1 gene polymorphisms. Two allelic variants (c.335T>C and c.3073A>C) were detected. The CC genotype of the c.335T>C polymorphism was associated with an increased risk of developing HCC compared to the TT genotype (OR = 2.161, 95%CI = 1.350-3.459, &#967;2 = 10.55, P = 0.0011). The risk of HCC was significantly higher for the CC genotype in the c.3073A>C polymorphism compared to the AA genotype in the studied populations (CCvs AA: OR = 2.575, 95%CI = 1.646-4.028, &#967;2 = 17.64, P < 0.0001). The C allele of the c.335T>C and c.3073A>C variants may contribute to the risk of HCC (Cvs T of c.335T>C: OR = 1.512, 95%CI = 1.208-1.893, &#967;2 = 13.07, P = 0.0003, and Cvs A of c.3073A>C: OR = 1.646, 95%CI = 1.322-2.049, &#967;2 = 20.03, P < 0.0001). The c.335T>C and c.3073A>C polymorphisms of the MDR1 gene were associated with the risk of occurrence of HCC in the Chinese Han population. Further investigations are needed to confirm these results in larger different populations.

Hepatitis B virus subgenotype C2- and B2-associated mutation patterns may be responsible for liver cirrhosis and hepatocellular carcinoma, respectively

The objective of this study was to examine hepatitis B virus (HBV) subgenotypes and mutations in enhancer II, basal core promoter, and precore regions of HBV in relation to risks of liver cirrhosis (LC) and hepatocellular carcinoma (HCC) in Southeast China. A case-control study was performed, including chronic hepatitis B (CHB; n=125), LC (n=120), and HCC (n=136). HBV was genotyped by multiplex polymerase chain reaction and subgenotyped by restriction fragment length polymorphism. HBV mutations were measured by DNA sequencing. HBV genotype C (68.2%) predominated and genotype B (30.2%) was the second most common. Of these, C2 (67.5%) was the most prevalent subgenotype, and B2 (30.2%) ranked second. Thirteen mutations with a frequency >5% were detected. Seven mutation patterns (C1653T, G1719T, G1730C, T1753C, A1762T, G1764A, and G1799C) were associated with C2, and four patterns (C1810T, A1846T, G1862T, and G1896A) were associated with B2. Six patterns (C1653T, G1730C, T1753C, A1762T, G1764A, and G1799C) were obviously associated with LC, and 10 patterns (C1653T, G1730C, T1753C, A1762T, G1764A, G1799C, C1810T, A1846T, G1862T, and G1896A) were significantly associated with HCC compared with CHB. Four patterns (C1810T, A1846T, G1862T, and G1896A) were significantly associated with HCC compared with LC. Multivariate regression analyses showed that HBV subgenotype C2 and C2-associated mutation patterns (C1653T, T1753C, A1762T, and G1764A) were independent risk factors for LC when CHB was the control, and that B2-associated mutation patterns (C1810T, A1846T, G1862T, and G1896A) were independent risk factors for HCC when LC was the control.

Esculetin, a coumarin derivative, exerts in vitro and in vivo antiproliferative activity against hepatocellular carcinoma by initiating a mitochondrial-dependent apoptosis pathway

This study investigated the in vitro and in vivo antiproliferative activity of esculetin against hepatocellular carcinoma, and clarified its potential molecular mechanisms. Cell viability was determined by the MTT (tetrazolium) colorimetric assay. In vivoantitumor activity of esculetin was evaluated in a hepatocellular carcinoma mouse model. Seventy-five C57BL/6J mice were implanted with Hepa1-6 cells and randomized into five groups (n=15 each) given daily intraperitoneal injections of vehicle (physiological saline), esculetin (200, 400, or 700 mg·kg-1·day-1), or 5-Fu (200 mg·kg-1·day-1) for 15 days. Esculetin significantly decreased tumor growth in mice bearing Hepa1-6 cells. Tumor weight was decreased by 20.33, 40.37, and 55.42% with increasing doses of esculetin. Esculetin significantly inhibited proliferation of HCC cells in a concentration- and time-dependent manner and with an IC50 value of 2.24 mM. It blocked the cell cycle at S phase and induced apoptosis in SMMC-7721 cells with significant elevation of caspase-3 and caspase-9 activity, but did not affect caspase-8 activity. Moreover, esculetin treatment resulted in the collapse of mitochondrial membrane potential in vitro and in vivo accompanied by increased Bax expression and decreased Bcl-2 expression at both transcriptional and translational levels. Thus, esculetin exerted in vitro and in vivo antiproliferative activity in hepatocellular carcinoma, and its mechanisms involved initiation of a mitochondrial-mediated, caspase-dependent apoptosis pathway.