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1.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;46(6): 513-520, 02/jul. 2013. graf
Article in English | LILACS | ID: lil-679201

ABSTRACT

Frogs have been used as an alternative model to study pain mechanisms. Since we did not find any reports on the effects of sciatic nerve transection (SNT) on the ultrastructure and pattern of metabolic substances in frog dorsal root ganglion (DRG) cells, in the present study, 18 adult male frogs (Rana catesbeiana) were divided into three experimental groups: naive (frogs not subjected to surgical manipulation), sham (frogs in which all surgical procedures to expose the sciatic nerve were used except transection of the nerve), and SNT (frogs in which the sciatic nerve was exposed and transected). After 3 days, the bilateral DRG of the sciatic nerve was collected and used for transmission electron microscopy. Immunohistochemistry was used to detect reactivity for glucose transporter (Glut) types 1 and 3, tyrosine hydroxylase, serotonin and c-Fos, as well as nicotinamide adenine dinucleotide phosphate diaphorase (NADPH-diaphorase). SNT induced more mitochondria with vacuolation in neurons, satellite glial cells (SGCs) with more cytoplasmic extensions emerging from cell bodies, as well as more ribosomes, rough endoplasmic reticulum, intermediate filaments and mitochondria. c-Fos immunoreactivity was found in neuronal nuclei. More neurons and SGCs surrounded by tyrosine hydroxylase-like immunoreactivity were found. No change occurred in serotonin- and Glut1- and Glut3-like immunoreactivity. NADPH-diaphorase occurred in more neurons and SGCs. No sign of SGC proliferation was observed. Since the changes of frog DRG in response to nerve injury are similar to those of mammals, frogs should be a valid experimental model for the study of the effects of SNT, a condition that still has many unanswered questions.


Subject(s)
Animals , Male , Ganglia, Spinal/metabolism , Ganglia, Spinal/ultrastructure , Oxidoreductases/metabolism , Proto-Oncogene Proteins c-fos/metabolism , Sciatic Nerve/injuries , Serotonin/metabolism , Cellular Microenvironment , Glucose Transport Proteins, Facilitative/metabolism , Immunohistochemistry , Microscopy, Electron, Transmission , NADPH Dehydrogenase/metabolism , Neuralgia/metabolism , Rana catesbeiana , /metabolism
2.
Arq. neuropsiquiatr ; Arq. neuropsiquiatr;66(2a): 242-245, jun. 2008. tab
Article in English | LILACS | ID: lil-484134

ABSTRACT

The effects of protein malnutrition on the quantitative aspects of the myenteric plexus in the ileum of adult Rattus norvegicus were assessed. Thirty 90-day-old rats were divided into two groups: Control Group (CG, n=15) and Experimental Group (EG, n=15). The CG received 26 percent protein chow and the EG received 4 percent protein chow for 90 days. At the end of the experiment, the animals from the CG weighed 369.63±26.33, and the ones from the EG 215.34±56.31. The ileum was submitted to Giemsa, NADH- and NADPH-diaphorase technique in order to evidence nervous cells in the whole-mount preparations. Animals from the EG presented a 41.75 percent body weight loss in relation to the CG as well as 17.6 percent length reduction for the ileum-jejunum. Moreover, the organ was 41 percent lighter for the EG. Giemsa-stained neurons were 17.02 percent more concentrated in the EG (p>0.05). NADH-diaphorase-stained neurons were 26.6 percent more concentrated in the EG (p<0.05), while the NADPH-diaphorase were 26.28 percent more concentrated in this group (p<0.05).


Avaliou-se o efeito da desnutrição protéica sobre o número de neurônios mientéricos do íleo de ratos adultos. Foram utilizados 30 animais (90 dias de idade), divididos em dois grupos: controle (GC, n=15) e experimental (GE, n=15), sendo oferecido ao GC ração com teor protéico de 26 por cento e, para o GE, ração com 4 por cento de proteína, durante 90 dias. Os animais do grupo controle pesaram 369,63±26,33g e o experimental 215,34±56,31g. Preparados de membrana do íleo foram submetidos à técnica de Giemsa, NADH- e NADPH-diaforase. Os animais do GE apresentaram perda de peso de 41,75 por cento, em relação ao GC e redução do comprimento do jejuno-íleo de 17,6 por cento, além disso, o órgão apresentou-se 41 por cento mais leve no GE. Os neurônios corados com a técnica de Giemsa apresentaram-se 17,02 por cento mais concentrados no GE (p>0,05). Os neurônios NADH-diaforase apresentaram-se 26,60 por cento mais concentrados no GE (p<0,05). E os neurônios NADPH-diaforase apresentaram-se 26,28 por cento mais concentrados neste grupo (p<0,05).


Subject(s)
Animals , Male , Rats , Ileum/innervation , Myenteric Plexus/cytology , NADPH Dehydrogenase/metabolism , Neurons/cytology , Protein Deficiency/metabolism , Body Weight , Cell Count , Ileum/enzymology , Myenteric Plexus/enzymology , Neurons/enzymology , Organ Size , Rats, Wistar
3.
Arq. bras. cardiol ; Arq. bras. cardiol;90(6): 388-395, jun. 2008. ilus, tab
Article in English, Portuguese | LILACS | ID: lil-485183

ABSTRACT

FUNDAMENTO: Otimização da veia safena na revascularização miocárdica. OBJETIVO: Apresentar a técnica no-touch de preparo da veia safena. Essa técnica consiste na retirada da veia safena do seu leito, com um pedículo de tecido adiposo, protegendo-a contra espasmos, sendo desnecessário distendê-la. MÉTODOS: Estudo prospectivo e randomizado, incluindo 156 pacientes submetidos a cirurgia de revascularização miocárdica. Comparação da técnica no-touch com duas outras técnicas: convencional e intermediária. Procedeu-se à avaliação da morfologia endotelial, utilizando a microscopia. A perviabilidade das pontes foi determinada com exame angiográfico num período médio de 18 meses após a operação. A enzima óxido nítrico sintetase endotelial (eNOS) foi identificada por meio do estudo imunohistoquímico. RESULTADOS: A avaliação morfológica mostrou integridade endotelial de 97 por cento nas veias do grupo no-touch; enquanto quase metade da superfície endotelial das veias tratadas pelas outras técnicas exibiu ausência de células endoteliais. A angiografia revelou perviabilidade de 95,4 por cento para as pontes do grupo no-touch, 88,9 e 86,2 por cento para as pontes do grupo convencional e intermediária, respectivamente. O estudo imunohistoquímico revelou a presença da eNOS nas três camadas que compõem a parede da veia no grupo no-touch e redução dessa enzima no grupo convencional. CONCLUSÃO: A integridade endotelial e a atividade da eNOS foram melhor preservadas com o uso da técnica no-touch. A proteção mecânica fornecida pelo tecido gorduroso circundante à veia e a atividade vasodilatadora e bloqueadora da agregação plaquetária causada pelo óxido nítrico podem ser responsáveis pela proteção da veia contra o espasmo, como também por sua alta perviabilidade imediata.


BACKGROUND: Optimization of the saphenous vein for myocardial revascularization. OBJECTIVE: To present the no-touch technique of the saphenous vein preparation. This technique consists of harvesting the vein with a pedicle of surrounding tissue, which protects the vein from spasms, obviating the need for distension. METHODS: A prospective, randomized study with 156 patients who underwent artery bypass grafting was performed comparing three saphenous vein harvesting techniques: conventional, intermediate, and no-touch. A morphological study of the endothelium was carried out using scanning microscopy. An angiographic assessment of the vein graft patency was performed at a mean follow-up time of 18 months. Also, an immunohistochemical assessment was carried out to identify the endothelial enzyme nitric oxide synthase (eNOS) in the vein wall RESULTS: The preservation of the endothelial cell integrity was greater in the no-touch technique than in the other procedures. At angiographic follow-up, the patency for the no-touch group was 95.4 percent, 88.9 percent for the grafts of the conventional technique group, and 86.2 percent for the grafts performed in the intermediate technique group. The immunohistochemical assessment revealed eNOS in all three layers of the vein wall in the no-touch group and reduction of this enzyme in the conventional group. CONCLUSION: The endothelial integrity and eNOS activity were better preserved when using the no-touch technique for vein graft harvesting. The mechanical protection provided by the cushion of surrounding tissue in the no-touch group, the vasorelaxation and thromboresistant activities of nitric oxide may be responsible for the reduction of vasospasms and improved patency rate.


Subject(s)
Aged , Female , Humans , Male , Middle Aged , Coronary Artery Bypass/methods , Endothelium, Vascular/ultrastructure , Nitric Oxide/metabolism , Saphenous Vein/transplantation , Tissue and Organ Harvesting/methods , Vascular Patency/physiology , Coronary Angiography , Coronary Artery Bypass/instrumentation , Follow-Up Studies , Graft Occlusion, Vascular , NADPH Dehydrogenase/metabolism , Nitric Oxide Synthase Type III/metabolism , Nitric Oxide Synthase/metabolism , Prospective Studies , Statistics, Nonparametric , Saphenous Vein/enzymology
4.
Pesqui. vet. bras ; Pesqui. vet. bras;28(2): 95-102, fev. 2008. ilus, graf, tab
Article in English | LILACS | ID: lil-481226

ABSTRACT

The relation between hyperglycemia and diabetic neuropathy has already been demonstrated in some studies. Among the theories proposed for its etiology the oxidative stress stands out. The performance of nitric oxide as a link between the metabolic and vascular neuropathogenic factors that triggers the diabetic neuropathy has already been put forward. This study aimed to assess the quantification and measurements of the cell body profile area (CBPA) of NADPH-diaphorase reactive (NADPH-dp) myenteric neurons of the jejunum of diabetic rats (induced by streptozotocin) supplemented with Ascorbic Acid (AA). These changes in the myenteric neurons seem to be related to the gastrointestinal disturbances observed in diabetes mellitus (DM). Twenty male Wistar rats (Rattus norvegicus) were distributed in 4 groups (n=5): controls (C), control supplemented (CS), diabetic (D), and diabetic suplemented (DS). DM was induced by estreptozotocin (50mg/kg body wt). One week after the induction and confirmation of the DM (glycemia exam), animals of the groups CS and DS received 50mg of AA three times a week by gavage. After 90 days of experiment, the animals were anesthetized with lethal thiopental dose (40mg/kg) and the collected jejunum processed for the histochemistry NADPH-diaphorase technique. Whole-mount preparations were obtained for quantitative and morphometric analysis of the myenteric neurons. A quantity of jejunum neurons in the Group D (96±7.5) was not different (P>0.05) from Group DS (116±8.08), C (92±9.7), and CS (81±5.4), but in Group DS the quantity was higher (P<0.05) than in Group C and CS. The CBPA of neurons from Group D (189.50±2.68µm²) and DS (195.92±3.75µm²) were lower (P<0.05) than from Group C (225.13±4.37µm²) and CS (210.23±3.15µm²). The streptozotocin-induced DM did not change the jejunum-ileum area, the jejunum myenteric plexus space organization and the density of NADPH-dp ...


A relação entre hiperglicemia e neuropatia diabética foi demonstrada em várias pesquisas. Entre as teorias propostas para sua etiologia destaca-se o estresse oxidativo. O papel do óxido nítrico como elo entre os fatores neuropatogênicos metabólico e vascular que ativam a neuropatia diabética tem sido ressaltado. Este estudo objetivou avaliar a quantificação e a morfometria da área do perfil do corpo celular (CBPA) de neurônios mioentéricos NADPH-diaforase reativos (NADPH-dp) do jejuno de ratos diabéticos e suplementados com Ácido Ascórbico (AA), uma vez que alterações nos neurônios mioentéricos parecem estar relacionadas aos distúrbios gastrointestinais observados no diabetes mellitus (DM). Vinte ratos machos da linhagem Wistar (Rattus norvergicus) foram distribuídos em 4 grupos (n=5): controle (C), controle suplementado (CS), diabético (D) e diabético suplementado (DS). O DM foi induzido através de injeção de estreptozootocina (50mg/kg de peso corporal). Uma semana depois da indução e confirmação do DM (glicemia), animais dos grupos CS e DS receberam, via gavagem, 50mg de AA três vezes por semana. Após 90 dias de período experimental, os animais foram anestesiados com dose letal de thiopental intravenosa (40mg/kg) e o jejuno foi retirado e processado para a técnica histoquímica da NADPH-diaforase. Preparados de membrana foram obtidos para análises quantitativa e morfométrica dos neurônios mioentéricos. A quantidade de neurônios do jejuno do Grupo D (96±7,5) não diferiu (P>0,05) dos Grupos DS (116±8,08), C (92±9,7) e CS (81±5,4), mas no Grupo DS o número de neurônios foi superior (P<0,05) aos Grupos C e CS. A CBPA de neurônios do Grupo D (189,50±2,68µm²) e DS (195,92±3,75µm²) foi menor (P<0,05) do que a dos Grupos C (225,13±4,37µm²) e CS (210,23±3,15µm²). O DM induzido por estreptozootocina não alterou a área do jejuno-íleo, a organização espacial do plexo mioentérico e a densidade...


Subject(s)
Animals , Male , Rats , Diabetes Mellitus, Experimental , Hyperglycemia/metabolism , Jejunum/anatomy & histology , Jejunum , NADPH Dehydrogenase/metabolism , Neurons , Myenteric Plexus , Rats, Wistar , Ascorbic Acid/administration & dosage , Ascorbic Acid/pharmacology , Streptozocin
5.
J. vet. sci ; J. vet. sci;: 143-150, 2006.
Article in English | WPRIM | ID: wpr-91386

ABSTRACT

Nitric oxide (NO) is a non-adrenergic, non-cholinergic neurotransmitter found in the enteric nervous system that plays a role in a variety of enteropathies, including inflammatory bowel disease. Alteration of nitrergic neurons has been reported to be dependent on the manner by which inflammation is caused. However, this observed alteration has not been reported with acetic acid-induced colitis. Therefore, the purpose of the current study was to investigate changes in nitrergic neuromuscular transmission in experimental colitis in a rat model. Distal colitis was induced by intracolonic administration of 4% acetic acid in the rat. Animals were sacrificed at 4 h and 48 h postacetic acid treatment. Myeloperoxidase activity was significantly increased in the acetic acid-treated groups. However, the response to 60 mM KCl was not significantly different in the three groups studied. The amplitude of phasic contractions was increased by Nomega-nitro-L-arginine methyl ester (L-NAME) in the normal control group, but not in the acetic acid-treated groups. Spontaneous contractions disappeared during electrical field stimulation (EFS) in normal group. However, for the colitis groups, these contractions initially disappeared, and then reappeared during EFS. Moreover, the observed disappearance was diminished by L-NAME; this suggests that these responses were NO-mediated. In addition, the number of NADPH-diaphorase positive nerve cell bodies, in the myenteric plexus, was not altered in the distal colon; whereas the area of NADPH-diaphorase positive fibers, in the circular muscle layer, was decreased in the acetic acidtreated groups. These results suggest that NO-mediated inhibitory neural input, to the circular muscle, was decreased in the acetic acid-treated groups.


Subject(s)
Animals , Male , Rats , Acetic Acid/toxicity , Colitis/chemically induced , Colon/drug effects , Indicators and Reagents/toxicity , Muscle Contraction/drug effects , Muscle, Smooth/drug effects , Myenteric Plexus/pathology , NADPH Dehydrogenase/metabolism , NG-Nitroarginine Methyl Ester/pharmacology , Neuromuscular Junction/drug effects , Nitrergic Neurons/drug effects , Nitric Oxide/metabolism , Peroxidase/metabolism , Potassium Chloride/pharmacology , Rats, Sprague-Dawley
6.
Yonsei med. j ; Yonsei med. j;: 123-128, 2004.
Article in English | WPRIM | ID: wpr-225870

ABSTRACT

This study was conducted to define the molecular mechanism of fasting-induced down-regulation of neuronal nitric oxide synthase (nNOS) expression in the hypothalamic paraventricular nucleus (PVN). Rats were adrenalectomized (ADX), and then either underwent food deprivation or received varying doses of dexamethasone for 48 h. The brain tissues were processed for NADPH-diaphorase (NADPH-d) staining, a histochemical marker of nNOS enzyme activity. Both the ADX and the sham operated rats showed a significant weight loss after 48 h of food deprivation. Food deprivation decreased the number of NADPH-d containing cells in the PVN of sham rats, however, not in the ADX rats. Dexamethasone dose- dependently decreased NADPH-d cells in the PVN of ADX rats. The effect of ADX or dexamethasone was limited to the parvocellular subdivision of PVN. These results suggest that the adrenal glucocorticoids may down-regulate nNOS expression in the PVN during food deprivation.


Subject(s)
Animals , Male , Rats , Adrenalectomy , Biomarkers , Dexamethasone/blood , Down-Regulation/physiology , Fasting/physiology , Food Deprivation/physiology , Glucocorticoids/blood , NADPH Dehydrogenase/metabolism , Nitric Oxide Synthase/metabolism , Paraventricular Hypothalamic Nucleus/enzymology , Rats, Sprague-Dawley
7.
Arq. neuropsiquiatr ; Arq. neuropsiquiatr;59(3A): 493-498, Sept. 2001. tab
Article in English | LILACS | ID: lil-295898

ABSTRACT

The aims of this work were to evaluate the effects of the deficient ingestion of protein and vitamin B on the biochemical and hematologic parameters and on the NADH- and NADPH-diaphorase positive myenteric neurons. The control animals (n=10) received commercial chow and the experimental rats (n=10) received chow with protein level reduced to 8 percent during 120 days. At the time of killing blood was collected for assessment of the blood and hematologic parameters and the ascending colon for quantitative analysis of the neurons of the myenteric plexus. It was observed that the reduction of the protein level to 8 percent coupled to the reduction of the levels of vitamin B in adult rats neither led to qualitative or quantitative changes on red or white blood cells, nor decreased globulin levels, induced the formation of edema or gave rise to clinical signs typical of protein or vitamin B deficiency. On the other hand, the experimental protocol led to less weight gain, change on the body composition with fat deposition; decrease of the values of serum total protein and albumin; reduction of the area of colon and density of nitrergic and NADH-diaphorase myenteric neurons inferior to the expected


Subject(s)
Animals , Male , Rats , Blood Cells/metabolism , Colon/innervation , Myenteric Plexus/metabolism , Protein Deficiency/metabolism , Vitamin B Deficiency/metabolism , Blood Cells/chemistry , Dihydrolipoamide Dehydrogenase/metabolism , Myenteric Plexus/chemistry , Myenteric Plexus/enzymology , NADPH Dehydrogenase/metabolism , Protein Deficiency/blood , Rats, Wistar , Vitamin B Deficiency/blood
8.
Yonsei med. j ; Yonsei med. j;: 215-219, 2001.
Article in English | WPRIM | ID: wpr-195973

ABSTRACT

Axotomy of the vagal motor neurons by cervical vagotomy induces NADPH diaphorase staining due to increased nitric oxide synthase expression in both the rat dorsal motor nucleus and nucleus ambiguous; furthermore, cerical vagotomy leads to cell death of the dorsal motor nucleus cells. Subdiaphragmatic vagotomy axotomizes the vagal motor cells further from the brainstem than cervical vagotomy, and cuts the fibers running only to the abdominal viscera. Here we report that subdiaphragmatic vagotomy is sufficient to induce NADPH diaphorase staining in the dorsal motor nucleus but does not induce staining in the nucleus ambiguus. Because the neurons of the dorsal motor nucleus do not undergo cell death after subdiaphragmatic vagotomy and are able to re-enervate the gut, the increased nitric oxide synthase expression after distal axotomy may be related more to regeneration than degeneration.


Subject(s)
Male , Rats , Animals , Fourth Ventricle/physiology , Fourth Ventricle/enzymology , Fourth Ventricle/cytology , Motor Neurons/enzymology , NADPH Dehydrogenase/metabolism , Rats, Sprague-Dawley , Vagotomy/methods , Vagus Nerve/physiology
9.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;32(11): 1429-36, Nov. 1999. graf, tab
Article in English | LILACS | ID: lil-248437

ABSTRACT

Injection of an Ascaris suum extract (Asc) affects both the humoral and cellular immune responses to unrelated antigens when it is co-administered with these antigens. In the present study we evaluated the effect of Asc on macrophage activation in the early phase of Mycobacterium bovis BCG (Pasteur strain TMCC 1173) infection in C57Bl/6 mice. C57Bl/6 mice were injected intraperitoneally (ip) with 0.1 mg BCG (BCG group) or BCG plus 1 mg Asc (BCG + Asc group). The peritoneal exudates were obtained at 2, 7 and 14 days after infection. The numbers of IFN-g-secreting cells were assessed by the ELISPOT assay. Nitric oxide (NO) production was measured by the Griess method and by the evaluation of NADPH diaphorase activity in the peritoneal exudates. The administration of Asc extract increased NADPH diaphorase activity (2 days: control = 0, BCG = 7 per cent, BCG + Asc = 13 per cent, and Asc = 4 per cent; 7 days: control = 4, BCG = 13 per cent, BCG + Asc = 21 per cent, and Asc = 4.5 per cent) and TNF-a levels (mean + or - SD; 2 days: control = 0, BCG = 169 + or - 13, BCG + Asc = 202 + or - 37, and Asc = 0; 7 days: control = 0, BCG = 545 + or - 15.5, BCG + Asc = 2206 + or - 160.6, and Asc = 126 + or - 26; 14 days: control = 10 + or - 1.45, BCG = 9 + or - 1.15, BCG + Asc = 126 + or - 18, and Asc = 880 + or - 47.67 pg/ml) in the early phase of BCG infection. Low levels of NO production were detected at 2 and 7 days after BCG infection, increasing at 14 days (mean + or - SD; 2 days: control = 0, BCG = 3.7 + or - 1.59, BCG + Asc = 0.82 + or - 0.005, Asc = 0.48 + or - 0.33; 7 days: control = 0, BCG = 2.78 + or - 1.54, BCG + Asc = 3.07 + or - 1.05, Asc = 0; 14 days: control = 0, BCG = 9.05 + or - 0.53, BCG + Asc = 9.61 + or - 0.81, Asc = 10.5 + or - 0.2 (2 x 106) cells/ml). Furthermore, we also observed that Asc co-injection induced a decrease of BCG-colony-forming units (CFU) in the spleens of BCG-infected mice during the first week of infection (mean + or - SD; 2 days: BCG = 1.13 + or - 0.07 and BCG + Asc = 0.798 + or - 0.305; 7 days: BCG = 1.375 + or - 0.194 and BCG + Asc = 0.548 + or - 0.0226; 14 days: BCG = 0.473 + or - 0.184 and BCG + Asc = 0.675 + or - 0.065 (x 102) CFU). The present data suggest that Asc induces the enhancement of the immune response in the early phase of BCG infection.


Subject(s)
Animals , Female , Mice , Antigens, Helminth/pharmacology , Ascaris suum/immunology , Macrophage Activation/drug effects , Mycobacterium bovis/drug effects , Spleen/microbiology , Stem Cells/drug effects , Tuberculosis/veterinary , NADPH Dehydrogenase/metabolism , Time Factors , Tumor Necrosis Factor-alpha/biosynthesis
10.
Indian J Physiol Pharmacol ; 1999 Jul; 43(3): 315-22
Article in English | IMSEAR | ID: sea-106393

ABSTRACT

Vasculogenesis was simultaneously studied with embryogenesis in in ovo chick embryo culture, which was harvested at 40 hours. Endodermal cells and vascular endothelial cells were studied using a new combination of stains, immunohistochemistry (for nuclei and basement membrane) and NADPH-diaphorase activity in whole-mounts, paraffin sections and etched semithin sections. The model can be used for the study of developmental process of blood vessels as well as embryonic physiology of blood vessels vis-a-vis organogenesis in response to different angiogenic agents, drug trials, cancer therapy by angiostatic chemicals/radiations and toxins. Considering that vasculogenesis/angiogenesis as one of the fundamental phenomena in physiology, pathophysiology, toxicology and pharmacology of developmental sciences, the model in developing embryo is presented.


Subject(s)
Animals , Culture Techniques , Endoderm/cytology , Immunohistochemistry , Models, Biological , NADPH Dehydrogenase/metabolism , Neovascularization, Physiologic
11.
Indian J Physiol Pharmacol ; 1999 Jul; 43(3): 305-14
Article in English | IMSEAR | ID: sea-108751

ABSTRACT

In vivo culture of chick embryo was carried out to develop an experimental interphase between in vitro and in vivo study of embryonic physiology. In the process, a simultaneous model of vasculogenesis and organogenesis has been worked out, which is impossible to achieve in mammalian system. Both early (40 hours of incubation) and late (64 & 88 hours of incubation) hours of cultures were conducted for morphological and morphometric studies. A new combination of stains was used in place of conventional haematoxylin and eosin in 40 hours old whole-mount of embryos. Semithin plastic sections were etched for haematoxylin/pyronin stain in addition to paraffin (both normal and enblock) sections. Specific stains (histological, enzyme histochemical or immunohistochemical) were chosen according to the specific organs/areas studied. Immunohistochemistry and NADPH-diaphorase activity were standardized in whole-mount of embryos. Morphometry was done using camera lucida and quantitative image analysis system. A parallel preparation of extra embryonic whole-mounts, paraffin and semithin plastic sections with different types of stainings provides evidence for the scope of the simultaneous study of vasculogenesis. Thus the morphological and morphometric data presented in this and the succeeding article describe the scope and avenues for the use of ex vivo model in various aspects of embryonic physiology, preliminary drug trials/metabolism, radiology, teratology and toxicology.


Subject(s)
Animals , Culture Techniques , Immunohistochemistry , Models, Biological , NADPH Dehydrogenase/metabolism , Peroxidases/metabolism , Somites/cytology
12.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;32(4): 489-93, Apr. 1999. ilus
Article in English | LILACS | ID: lil-231743

ABSTRACT

Seven days after transection of the sciatic nerve NADPH-diaphorase activity increased in the small and medium neurons of the dorsal root ganglia of the turtle. However, this increase was observed only in medium neurons for up to 90 days. At this time a bilateral increase of NADPH-diaphorase staining was observed in all areas and neuronal types of the dorsal horn, and in positive motoneurons in the lumbar spinal cord, ipsilateral to the lesion. A similar increase was also demonstrable in spinal glial and endothelial cells. These findings are discussed in relation to the role of nitric oxide in hyperalgesia and neuronal regeneration or degeneration.


Subject(s)
Animals , Male , Female , Axotomy , Ganglia, Spinal/enzymology , NADPH Dehydrogenase/metabolism , Spinal Cord/enzymology , Turtles , Hyperalgesia , Lumbosacral Region , Nerve Degeneration , Nerve Regeneration , Sciatic Nerve
13.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;31(9): 1157-61, sept. 1998.
Article in English | LILACS | ID: lil-222964

ABSTRACT

The effects of methylmercury (MeHg) on histochemical demonstration of the NADPH-diaphorase (NADPH-d) activity in the striate cortex were studied in 4 adult cats. Two animals were used as control. The contaminated animals received 50 ml milk containing 0.42 µg MeHg and 100 g fish containing 0.03 µg MeHg daily for 2 months. The level of MeHg in area 17 of intoxicated animals was 3.2 µg/g wet weight brain tissue. Two cats were perfused 24 h after the last dose (group 1) and the other animals were perfused 6 months later (group 2). After microtomy, sections were processed for NADPHd histochemistry procedures using the malic enzyme method. Dendritic branch counts were performed from camera lucida drawings for control and intoxicated animals (N = 80). Average, standard deviation and Student t-test were calculated for each data group. The concentrations of mercury (Hg) in milk, fish and brain tissue were measured by acid digestion of samples, followed by reduction of total Hg in the digested sample to metallic Hg using stannous chloride followed by atomic fluorescence analysis. Only group 2 revealed a reduction of the neuropil enzyme activity and morphometric analysis showed a reduction in dendritic field area and in the number of distal dendrite branches of the NADPHd neurons in the white matter (P<0.05). These results suggest that NADPHd neurons in the white matter are more vulnerable to the long-term effects of MeHg than NADPHd neurons in the gray matter.


Subject(s)
Cats , Animals , Methylmercury Compounds/poisoning , NADPH Dehydrogenase/metabolism , Neuropil/enzymology , Visual Cortex/drug effects , Visual Cortex/enzymology , Fluorescence , Mercury/analysis , Microtomy , Neurons/drug effects , Neurons/pathology , Neuropil/drug effects , Neuropil/pathology , Visual Cortex/pathology
14.
Rev. bras. colo-proctol ; 18(1): 52-7, jan.-mar. 1998. ilus, tab
Article in Portuguese | LILACS | ID: lil-219919

ABSTRACT

A fisiopatologia da Doença de Chagas ainda näo está completamente esclarecida. O óxido nítrico (NO) tem sido citado como neurotransmissor responsável pelo relaxamento do esfíncter interno do ânus no indivíduo normal. Neuronal nicotinamida adenina dinucleotídeo fosfato (NADPH) diaforase pode ser usado como marcador neuronal do NO. Objetivos: Examinar as alteraçöes nos neurônios produtores de NO do cólon de pacientes submetidos à ressecçäo por megacólon avançado e comparar com o intestino delgado dos mesmos pacientes e com controles. Métodos: Espécimes obtidos da ressecçäo do reto e biópsias extramucosas do intestino delgado de 11 pacientes chagásicos foram comparadas a 10 pacientes controles com câncer de cólon. Os tecidos foram fixados em soluçäo de Zamboni e submetidos à histoquímica para neurônios contendo NADPH diaforase. A reatividade foi avaliada utilizando-se uma escala de 0 a 4 nas diversas camadas da parede intestinal: musculatura lisa longitudinal (ML), plexo mioentérico (PM), musculatura lisa circular (MC), plexo submucoso (PSM), e mucosa (M). Resultados: Os casos controles mostraram os plexos mioentérico e submucoso bem corados e uma rica rede de terminaçöes nervosas nas camadas musculares. Os espécimes provenientes de doentes chagásicos revelaram uma diminuiçäo da reatividade e da coloraçäo em todas as camadas do intestino. De maneira geral, houve uma diminuiçäo estatisticamente significante nos neurônios contendo NADPH diaforase. O intestino delgado clinicamente näo envolvido também demonstrou diminuiçäo da reatividade, porém em menor grau. Conclusöes: A atividade da NADPH diaforase está diminuída em pacientes com megacólon avançado, especialmente no plexo mioentérico e na camada muscular lisa; 2. Houve também uma diminuiçäo da atividade neuronal do NO no jejuno clinicamente näo envolvido pela doença, mas em menor grau


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Chagas Disease/physiopathology , Immunohistochemistry , Intestine, Large/physiopathology , Megacolon/physiopathology , Megacolon/surgery , NADPH Dehydrogenase/analysis , NADPH Dehydrogenase/metabolism , Nitric Oxide Synthase/analysis , Nitric Oxide/analysis , Enteric Nervous System/physiopathology , Colorectal Neoplasms/chemistry , Chagas Disease/enzymology , Hirschsprung Disease/physiopathology , Fissure in Ano/drug therapy , Intestine, Large/enzymology , Intestine, Large/surgery , Intestine, Small/chemistry , Intestine, Small/enzymology , Megacolon/enzymology , Nitric Oxide Synthase/metabolism , Nitroglycerin/therapeutic use , Peristalsis , Enteric Nervous System/enzymology , Enteric Nervous System/chemistry , Vasodilator Agents/therapeutic use
15.
Yonsei med. j ; Yonsei med. j;: 125-132, 1997.
Article in English | WPRIM | ID: wpr-55514

ABSTRACT

Recent evidence implicates NO (Nitric oxide) as the principal mediator in an erection. To investigate the role of NO in the human erectile function, we studied the distribution pattern of nitroxergic fibers in the corpus cavernosum specimens obtained from 38 men using nicotinamide adenine dinucleotide phosphate diaphorase (NADPH-d) histochemistry. Diffusely scattered delicate nerve fibers showing blue color reaction after NADPH-d histochemical staining were observed in normal control specimens from potent men. The neurogenic impotence group showed a statistically-significant decrease in the number of positive fibers compared to the normal control group. The number of positive fibers in the non-neurogenic impotence group was decreased compared to the normal control group but was statistically insignificant. With nitric oxide synthase (NOS) immunohistochemical stain, immunoreactive nerve bundles were easily seen in normal control specimens from potent men. NOS immunoreactive nerve bundles were contained within the corpus cavernosa which stained with NADPH-d reaction. Our results suggest that nitric oxide, a potent smooth muscle relaxing neurotransmitter in the autonomic nervous system, plays a physiologic role in erectile function and NADPH-d enzyme histochemical staining on the biopsied corpus cavernosum may be used as an important diagnostic method in the evaluation of neurogenic impotence.


Subject(s)
Humans , Male , Histocytochemistry , Erectile Dysfunction/enzymology , NADPH Dehydrogenase/metabolism , Nitric Oxide Synthase/metabolism , Penis/enzymology , Tissue Distribution
16.
Ciênc. cult. (Säo Paulo) ; 48(1/2): 68-74, Jan.-Apr. 1996. ilus, graf
Article in English | LILACS | ID: lil-191245

ABSTRACT

Neurospora crassa conidiation and other microorganism differentiation processes can be explained as a response to a hyperoxidant state. Many proteins, among them NADP-glutamate dehydrogenase and glutamine synthetase, were oxidatively modiried and degraded at the start of all three morphogenetic transitions of the conidiation process. A shift in the redox state of the main cellular electron carriers, from a highly reduced state to a predominantly oxidized one, occurred stepwise with a highly oxidizing event at the start of each transition. Catalase activity increased during cell differentiation in various microorganisms and one of two catalases accumulated to a high level in the differentiated cell. Catalases in Neurospora were oxidized in vitro and in vivo giving rise to active enzyme conformers. Carotenoids, which have antioxidant functions in fungi, were consumed in each morphogenetic stage and oxidized carotenoids accumulated in differentiated cells. Carotenoid biosynthesis was induced following oxidative stress and during conidiation in each new cell structure. Increased generation of reactive oxygen species was detected by chemiluminescence at the onset of all transitions during differentiation. Antioxidants inhibited both light emission and cell differentiation. These and other data from the literature are discussed in the context of the Dioxygen Avoidance Theory of cell differentiation.


Subject(s)
Reactive Oxygen Species , Glutamate-Ammonia Ligase/metabolism , NADPH Dehydrogenase/metabolism , Neurospora crassa/enzymology , Oxidative Stress , Cell Differentiation , Luminescent Measurements , Neurospora crassa/growth & development , Oxidation-Reduction
17.
Medicina (B.Aires) ; Medicina (B.Aires);56(2): 169-72, 1996. tab, graf
Article in English | LILACS | ID: lil-172301

ABSTRACT

Neuropathological mechanisms triggered by excitatory aminoacids are Known to involve nitric oxide (NO). Neurons containing NO are histochemically reactive to nicotinamide adenine dinucleotide phosphate diaphorase (NADPH-d), which labels NO synthase in CNS, Sprague-Dawley male rats subjected to perinatal asphyxia (PA) at 37 degreese Celsius, and PA plus 15 degreese Celsius hypothermia were evaluted when 6 months old by NADPH-d histochemical reaction. Computarized image analysis was used for quantification of stained sections. NADPH-d neurons in striatum from subsevere and severe PA showed a significant increment in soma size and dendritic process length versus control and hypothermic treated rats. Post-ischemic damage reurons are therefore involved in NO changes induced by PA that may be prevented by hypothermia treatment.


Subject(s)
Animals , Male , Infant, Newborn , Rats , Asphyxia Neonatorum/metabolism , Corpus Striatum/metabolism , NADPH Dehydrogenase/metabolism , Neurons/metabolism , Nitric Oxide/metabolism , Analysis of Variance , Animals, Newborn , Hypothermia, Induced , Rats, Sprague-Dawley , Time Factors
18.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;28(7): 787-90, July 1995. ilus
Article in English | LILACS | ID: lil-155263

ABSTRACT

The primary somatosensory area (S1) of rodents presents multicellular units called barrels which can be identified by different techniques (e.g., Nissl staining, cytochrome oxidase or succinate dehydrogenase histochemistry). We applied NADPH diaphorase histochemistry to tangential sections of rat neocortex to determine if the reactive neuropil also shows the same remarkable array observed with other techniques. We demonstrated NADPH diaphorase-positive barrels in all hemispheres tested. The barrels are recognized as patches where the neuropil is most reactive. Each barrel is separated from the other by a less labeled neuropil. Many NADPH diaphorase-positive neurons are seen along the section, but very few cells are found in the barrel fild. In this region, most of the labeled neurons are localized in the less reactive region between the barrels, although a few NADPH diaphorase-positive cells can also be found insede the barrels


Subject(s)
Animals , Rats , NADPH Dehydrogenase/metabolism , Somatosensory Cortex/anatomy & histology , Histocytochemistry , Somatosensory Cortex/metabolism
19.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;27(10): 2431-5, Oct. 1994. graf
Article in English | LILACS | ID: lil-152624

ABSTRACT

The distribution of NADPH-diaphorase reactive cells was evalutated both in horizontal sections of a flattended cortex and in transversal sections of the opossum (Didelphis marsupialis) neocortex. The tangential distribution of labeled cells behind the orbitalis fissure was denser in the rostral vs caudal regions and in the lateral vs medial regions. Transversal sections revealed that most of the positive neurons are in the grey matter, although 1/4 of this population is located in the underlying white matter. This pattern of neuronal distribution is similar to that previously described in rodents, but quite different from that observed in higher mammals such as the cat and primates


Subject(s)
Animals , Cerebral Cortex/enzymology , NADPH Dehydrogenase/metabolism , Cell Count , Cerebral Cortex/pathology , Neurons/enzymology , Opossums
20.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;26(12): 1325-35, Dec. 1993. ilus, graf
Article in English | LILACS | ID: lil-148838

ABSTRACT

1. Electrical field stimulation (EFS) of intrinsic nerves in the rat proximal duodenum induces a frequency-dependent non-adrenergic-non-cholinergic (NANC) relaxation response. 2. The inhibitors of L-arginine-NO synthase L-NG-nitro arginine methyl-ester (L-NAME) and L-NOARG (L-NG-nitro arginine) reduced the NANC relaxations elicited by EFS in a dose- and time-dependent manner; L-NOARG was two times more potent than L-NAME (IC50 = 14.3 vs 25.2 microM) and these effects were partially reverted by the addition of 300-1000 microM L-arginine but not of 300-1000 microMD-arginine. Relaxation caused by vasoactive intestinal peptide (VIP; 0.1 microM) or ATP (20 microM) was not blocked by L-NAME or L-NOARG. 3. The magnitude of the blockade caused by L-NAME and L-NOARG was dependent on the frequency of stimulation. At low frequencies (below 1 Hz) both L-NAME and L-NOARG abolished the relaxations, while at 2 to 8 Hz only partial inhibition was observed (maximal inhibition: 44.6 per cent +/- 5.2 and 63.4 per cent +/- 3.4, respectively) 4. The basal tonus of the duodenum was increased by 10-300 microM L-NAME and 10-300 microM L-NOARG and this effect was blocked by 1 mM L-arginine. 5. Nitric oxide generated from acidified NaNO2 caused a dose-dependent (EC50 = 2.75 microM) relaxation of the duodenum which was not affected by 100 microM L-NAME, 100 microM L-NOARG or 1 microM tetrodotoxin (TTX). 6. NADPH-diaphorase positive neurons and fibers identified by histochemistry were present in the myenteric plexus and along both circular and longitudinal muscle fibers indicating that nitric oxide could be synthetized by these neural structures


Subject(s)
Animals , Male , Rats , Arginine/analogs & derivatives , Duodenum/physiology , Nitric Oxide/metabolism , Arginine/pharmacology , Dose-Response Relationship, Drug , Duodenum/drug effects , Electric Stimulation , Muscle Relaxation/drug effects , NADPH Dehydrogenase/metabolism , Rats, Wistar
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