Induction of apoptotic lesions in liver and lymphoid tissues and modulation of cytokine mRNA expression by acute exposure to deoxynivalenol in piglets

Six 1-month-old piglets were intravenously injected with deoxynivalenol (DON) at the concentration of 1 mg/kg body weight, with three pigs each necropsied at 6 and 24 h post-injection (PI) for investigation of hepatotoxicity and immunotoxicity with special attention to apoptotic changes and cytokine mRNA expression. Histopathological examination of the DON-injected pigs revealed systemic apoptosis of lymphocytes in lymphoid tissues and hepatocytes. Apoptosis of lymphocytes and hepatocytes was confirmed by the TdT-mediated dUTP-biotin nick end-labeling (TUNEL) method and immunohistochemical staining against single-stranded DNA and cleaved caspase-3. The number of TUNEL-positive cells in the thymus and Peyer's patches of the ileum was increased at 24 h PI compared to 6 h PI, but the peak was at 6 h PI in the liver. The mRNA expression of interleukin (IL)-1beta, IL-6, IL-18, and tumor necrosis factor (TNF)-alpha in the spleen, thymus and mesenteric lymph nodes were determined by semi-quantitative RT-PCR, and elevated expression of IL-1beta mRNA at 6 h PI and a decrease of IL-18 mRNA at 24 h PI were observed in the spleen. IL-1beta and IL-6 mRNA expressions increased significantly at 6 h PI in the thymus, but TNF-alpha decreased at 6 h PI in the mesenteric lymph nodes. These results show the apoptosis of hepatocytes suggesting the hepatotoxic potential of DON, in addition to an immunotoxic effect on the modulation of proinflammatory cytokine genes in lymphoid organs with extensive apoptosis of lymphocytes induced by acute exposure to DON in pigs.

Modulatory effects of chitosan adipate on the T and B lymphocyte subsets in mice

This study examined the subsets of T lymphocytes in the thymus, spleen and mesenteric lymph nodes as well as the subsets of B lymphocytes in the spleen and mesenteric lymph nodes in mice administered chitosan adipate (20 mg/kg) intraperitoneally once or four times at 24 h intervals. The results showed that chitosan adipate decreased the percentage of immature CD4+CD8+ thymic T cells and increased the percentage of mature CD4+ and CD8+ thymocytes. The most significant stimulating effect was observed after four injections. A single exposure to chitosan adipate increased the percentage of CD4+ mesenteric lymph node cells, but four injections of the drug increased the percentage of CD4+ and CD8+ mesenteric lymph node cells. Chitosan adipate had no effect on the subset of splenic T cells. In contrast, chitosan adipate administered either once or four times increased the percentage of CD19+ splenocytes but had no effect on the percentage of CD19+ mesenteric lymph node cells. Overall, chitosan adipate induces the maturation and differentiation of thymocytes, and regulates the number of B splenic cells and lymph node T cells irrespective of the number of doses.

Histological and biochemical study on the effect of the neuropeptide [substance P] and its antagonist [spantide] on the lymphoid tissue of the lung and spleen of rats

The role of substance P in immune regulation has been reported by numerous studies, however it is complex and not fully elucidated. This study focused on its role in the mediation of release of cytokines and immunoglobulins and initiation of proliferative changes in the lymphoid tissue of the lung and spleen. Ninety rats were divided into three groups, each of thirty: Group I was injected with endotoxin free water [as control], Group II was injected with substance P and Group III was injected with substance P and spantide. Fifteen rats from each group were sacrificed after two hours and the other 15 after one week. The levels of interleukins I and 6 and immunoglobulins G and M were determined. Histological examination was performed for the spleen and lung revealing that the proliferation of the lymphoid tissue in both organs was more marked in the group sacrificed after one week. Interleukins I and 6 and immunoglobulins G and M showed significant increase in group II as compared with group I and III after two hours of injection as well as after one week. These findings suggested that the substance P-mediated release of interleukins I and 6 with production of immunoglobulins G and M and the proliferation of lymphoid tissue of the lung and spleen can be partially inhibited by spantide

Modulation of gamma glutamyl transpeptidase activity in lymphoid system by organochlorine pesticides in rats.

Effects of 1,1,1,-trichloro-2,2-bis (p-chlorophenyl) ethane (DDT) and lindane were studied on gamma glutamyl transpeptidase (GGT) activity in different tissues of the lymphoid system in rats. DDT (100 or 200 ppm) and lindane (30 or 80 ppm) exposure for 8 weeks suppressed the GGT activity in a dose dependent manner in thymus and macrophage. In spleen, significant decrease in the enzyme activity was observed at higher exposure (200 ppm DDT or 80 ppm lindane) levels. Lindane suppressed GGT activity at both 30 or 80 ppm dose levels, while DDT reduced the GGT activity at 200 ppm but not at 100 ppm exposure in lymphocyte. The study indicates the possibility of using GGT as an effective and consistent biochemical marker for immunotoxicity of xenobiotics and other environmental stressors.

Effects of stress on gamma glutamyl transpeptidase (GGT) activity in lymphoid system of rats: modulation by drugs.

Effects of stress and its modulation by adaptogens were evaluated on gamma glutamyl transpeptidase (GGT) activity in different tissues of the lymphoid system in rats. Restrain stress (RSx5) suppressed the GGT activity in different tissues of lymphoid system viz. the lymphocyte, the spleen, the thymus and the macrophage, and the maximum effect was seen in the spleen. Chlordiazepoxide, a prototype anti-stress agent, which did not alter GGT activity per se, reversed the effect of RS on this enzyme activity in tissues of lymphoid system studied. Azardirachta indica (Al, Neem), an indigenous adaptogen stimulated the GGT activity per se and nearly normalised RS induced suppression of GGT in lymphoid system. The observed suppression of GGT activity in lymphoid system by stress and its modulation by natural and synthetic adaptogens indicates that GGT could be a consistent cellular/biochemical marker of stress responsiveness and stress-induced immunomodulation.

Alteraçöes metabólicas e funcionais em células e órgäos do sistema imunológico de ratos induzidas pela administraçäo intragástrica do óleo de peixe / Metabolic and functional changes in cells and organs of immune system of rats due to the fish oil administrated by gavage

O consumo de cápsulas de óleo de peixe (OP) por humanos visa a atenuaçäo dos sintomas e prevençäo de várias patologias. As alteraçöes metabólicas e funcionais em células e órgäos do sistema imunológico causadas pelo OP pela administraçäo intragástrica (AIG) foram avaliadas. Ratos recém-desmamados (50-70 g) foram submetidos a AIG diária com óleo de peixe, óleo de soja ou manteiga de cacau (0,4 por cento do peso), por 28 dias. Os dados da AIG do OP foram também comparados com os da dieta enriquecida com OP. Foram avaliados: aumento de permeabilidade vascular (reaçäo anafilática), funcionalidade de macrófagos (produçäo de 'H IND. 2O IND. 2', 'O IND. 2' e fagocitose), proliferaçäo de linfócitos, a atividade máxima das enzimas: hexoquinase, glicose-6-fosfato desidrogenase, citrato sintase (metabolismo de glicose), catalase, glutationa peroxidase e superóxido dismutase (antioxidantes) no baço, linfonodo mesentérico e timo. A concentraçäo de TBARs nos mesmos órgäos e no plasma e a capacidade antioxidante do plasma foram também determinadas

Effect of RN-301 immunomodulator on bronchus-associated lymphoid tissue (Balt) in protein depleted rats at weaning

It has been previously demonstrated in Wistar rats that severe protein deprivation at weaning, even after refeeding with a 20 percent casein diet for 21 days, provokes alterations in IgA+ B cell and T cell populations from gut and GALT (gut associated lymphoid tissue) that are reverted by immunomodulator IM-104. In the present report, we investigated the influence of RN-301 (quite similar to IM-104) given by the oral or subcutaneous route during the protein deprivation period, in the seeding of BALT with IgA+ B and CD5+T cells. The immunomodulator RN-301 contains LPS from E. coli and membrane and ribosomal fractions of P. acne. Tissue sections of the lower respiratory tract were studied by immunohistochemistry. The immunomodulator RN-301 administered by the oral route favours the significant increase in the seeding of the BALT lamina propria with IGA+B and CD5+T cells (p < 0.001). However, the RN-301 given by the subcutaneous route does not favour the repopulation of the BALT lamina propria. The ribosomal fractions from P. acne associated with LPS from E. coli contained in the immunomodulator RN-301 administered by the oral route may rescue the small resting lymphocytes in the gut-associated lymphoid tissue (GALT). This event favours their proliferation and migration to the BALT.

Modulatory effects of metanil yellow on immunity in rodents.

Pathomorphological and immunological studies were carried out on rodents following oral administration of 0, 0.1, 0.25 and 0.5% (w/w) metanil yellow, mixed in diet, for 30 days. No significant change in hematologic parameters and histologic architecture of liver, kidney, mesenteric lymph node, thymus and urinary bladder was observed except for mild desquamation of intestinal villi and moderate changes in Peyer's patches of small intestine with higher doses. Among immunological parameters, significant enhancement in the primary humoral immune response (anti-SRBC IgM plaque forming cells of spleen) was observed with the lowest dose of metanil yellow while higher doses produced opposing effects. An elevated cutaneous delayed type hypersensitivity (DTH) reaction to SRBC was seen in 0.1% metanil yellow treated animals but higher doses did not influence the reaction. The treatment also caused changes in functional capabilities of macrophages. Although these immune alterations could hardly influence the local immunity of gut, as measured by the capacity of animals to cause rejection of Nippostrongylus brasiliensis parasite, the potential to modulate the immunity in general by metanil yellow however assumes considerable biological significance.

Imunossupressäo experimental em camundongos: aspectos histopatológicos dos órgäos linfóides após tratamento com dexametasona e inoculaçäo de Candida albicans / Experimental imunossupressin in mice: histologycal aspects of the linfoid tissue after administration of dexamethasone and inoculation with Candida albicans

Foi realizada imunossupressäo experimental com corticosteróides em camundongos usando 1 mg/kg/dia de exametsona durante uma semana. Para verificar os efeitos imunossupressores da droga, sobre os tecidos linfóides, inoculamos 1 ml de 1.10 de Candida albicans, por via endovenosa, após o tratamento. Observamos a instalaçäo e evoluçäo da infecçäo durante doze dias e analisamos os aspectos histológicos do baço, timo, linfonodos, rins, fígado, pulmöes e pele, que foram retirados, em intervalos regulares, de animais tratados somente com dexametasona e somente com Candida albicans, ou com ambos os dois tratamentos. Os resultados obtidos nos levaram a concluir que ocorre imunossupressäo com essa dosagem de dexametasona e que o baço foi o órgäo mais atingido. A candidíase isoladamente também provocou imunossupressäo, afetando principalmente o timo. Os efeitos imunossupressores dos dois tratamentos se somaram quando houve a associaçäo dos mesmos

Time dependent effects of hormones on rate of protein synthesis in lymphoid organs of chickens.

Total protein content in blood serum and different lymphoid organs, such as bursa, spleen and thymus was investigated in chickens at two different circadian stages (0800 or 1600 hrs; early or late photophase) following administration of either saline or hormones (thyroxine or hydrocortisone or epinephrine). The results suggest that the lymphoid organs may respond differently to the exogenous administration of different hormones depending on the time of their administration.

"Effects of testosterone and stilbestrol on the liver and lymphoreticular system schistosoma infected mice"

The effects of stilbestrol d testosterone on schistosoma infected mice were studied. Stilbestrol increased the death rate of infected mice, aggravated the schistosomal hyperplasia. Testosterone, on the other hand, significantly diminished the death rate, protected the liver from many of the deleterious effects produced by schistosomasis and minimized the stimulating effect on the lymphoreticular system. The role played by stilbestrol on lymphoreticular hyperplasia and its possible relation to lymphoma in schistosoma infected patients is discussed. The possible therapeutic value of the male hormone, testosterone, in males infected with schistosomiasis is suggested and the possible danger of contraceptive pills [containing oestrogen] in females infected with schistosomiash is raised