Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 9 de 9
Filter
1.
Acta cir. bras ; 29(11): 742-747, 11/2014. graf
Article in English | LILACS | ID: lil-728644

ABSTRACT

PURPOSE: We evaluated the hypothesis that induced perioperative hypothermia (32 ± 1ºC) affects the redox balance in the tissue of colonic anastomosis in rats by modifying biochemical enzymatic and non-enzymatic markers related to oxidative stress. METHODS: Forty-eight male Wistar rats were randomly divided into eight experimental groups of six animals each and underwent laparotomy, sigmoid section and immediate anastomosis. Four groups were operated under normothermia (36 ± 1ºC), and the other four under hypothermia (32 ± 1ºC). The animals were reoperated on days 3, 7 and 14 postoperatively, and two groups underwent SHAM at 3 days. From the scar tissue samples, the activity of the antioxidant enzymes superoxide dismutase (SOD) and catalase (CAT) was evaluated, and the levels of non-enzymatic markers of oxidative stress, such as reduced glutathione (GSH) and lipid peroxidation, were measured by the thiobarbituric acid reactive substances (TBARS) assay. The means were compared between groups corresponding to each day of sampling and euthanasia. RESULTS: The hypothermic groups showed a significant reduction on the activity of SOD on day 7 postoperatively, on the activity of CAT on days 7 and 14 postoperatively and on the levels of GSH on day 7 postoperatively. The level of lipid peroxidation was increased in the hypothermia group on day 7 postoperatively and decreased on day 14 compared with the normothermic groups. CONCLUSION: Perioperative hypothermia reduced the activity of the antioxidant enzymes catalase and superoxide dismutase, glutathione levels and increased lipid peroxidation in the scar tissue of colonic anastomoses in rats. .


Subject(s)
Animals , Male , Colon/surgery , Hypothermia, Induced/adverse effects , Reactive Oxygen Species/metabolism , Wound Healing/physiology , Anastomosis, Surgical , Catalase/metabolism , Colon/enzymology , Glutathione/metabolism , Lipid Peroxidation , Oxidation-Reduction , Oxidative Stress/physiology , Postoperative Period , Random Allocation , Rats, Wistar , Superoxide Dismutase/metabolism , Time Factors
2.
Journal of Veterinary Science ; : 387-393, 2013.
Article in English | WPRIM | ID: wpr-197115

ABSTRACT

Prebiotics modulate microbial composition and ensure a healthy gastrointestinal tract environment that can prevent colon cancer development. These natural dietary compounds are therefore potential chemopreventive agents. Thirty Sprague-Dawley rats (4 months old) were experimentally treated with procarcinogen dimethylhydrazine to induce colon cancer development. The rats were randomly assigned to three groups: a control group (CG), a group treated with dimethylhydrazine (DMH), and a group given DMH and inulin, a prebiotic (DMH+PRE). The effects of inulin on the activities of bacterial glycolytic enzymes, short-chain fatty acids, coliform and lactobacilli counts, cytokine levels, and cyclooxygenase-2 (COX-2) and transcription nuclear factor kappa beta (NFkappaB) immunoreactivity were measured. Inulin significantly decreased coliform counts (p < 0.01), increased lactobacilli counts (p < 0.001), and decreased the activity of beta-glucuronidase (p < 0.01). Butyric and propionic concentrations were decreased in the DMH group. Inulin increased its concentration that had been reduced by DMH. Inulin decreased the numbers of COX-2- and NFkappaB-positive cells in the tunica mucosae and tela submucosae of the colon. The expression of IL-2, TNFalpha, and IL-10 was also diminished. This 28-week study showed that dietary intake of inulin prevents preneoplastic changes and inflammation that promote colon cancer development.


Subject(s)
Animals , Female , Male , Rats , Bacterial Proteins/genetics , Colon/enzymology , Colonic Neoplasms/chemically induced , Colony Count, Microbial , Cyclooxygenase 2/genetics , Cytokines/blood , Diet , Dietary Supplements/analysis , Dimethylhydrazines/toxicity , Enterobacteriaceae/drug effects , Fatty Acids, Volatile/genetics , Gene Expression Regulation/drug effects , Inulin/administration & dosage , Lactobacillaceae/drug effects , NF-kappa B/genetics , Prebiotics/analysis , Rats, Sprague-Dawley
3.
Article in English | IMSEAR | ID: sea-135672

ABSTRACT

Background & objectives: Clostridium difficile-associated disease (CDAD) remains an important nosocomial ailment. Antimicrobial therapy used for CDAD gives inconsistent results. This experimental study was planned to investigate the beneficial effects of Lactobacillus acidophilus and epidermal growth factor (EGF) for CDAD management. Methods: Among 10 groups of BALB/c mice (6 in each), group 1 served as controls receiving no inoculum. Animals in groups 2-10 received C. difficile, those in groups 3, 6 and 9 received L. acidophilus and those in groups 4, 7 and 10 received EGF after C. difficile inoculation. Animals in groups 5-7 were pre-treated with ampicillin and those in groups 8-10 with lansoprazole prior to C. difficile. The animals were killed and investigated for colonisation by C. difficile and toxin production, myeloperoxidase (MPO) activity and histopathology. Results: Colonisation by C. difficile was found to be significantly different (P<0.001) in the various groups. C. difficile toxin titres and MPO activity were significantly lower in animals given L. acidophilus and EGF after ampicillin (groups 6 and 7) and lansoprazole (groups 9 and 10). The severity of acute inflammation was also significantly less (P<0.05) in caecal and colonic segments of animals in groups 6 and 7 compared to those in group 5. Although the severity of acute inflammation was less in the caecal and colonic segment of animals in groups 9 and 10, the reduction was not significant compared to group 8. Interpretation & conclusions: Our findings showed that the administration of L. acidophilus and EGF reduced the severity of C. difficile infection in the experimental animals.


Subject(s)
2-Pyridinylmethylsulfinylbenzimidazoles/administration & dosage , Ampicillin/administration & dosage , Animals , Cecum/enzymology , Cecum/microbiology , Clostridioides difficile/pathogenicity , Colon/enzymology , Colon/microbiology , Disease Models, Animal , Enterocolitis, Pseudomembranous/diet therapy , Enterocolitis, Pseudomembranous/drug therapy , Enterocolitis, Pseudomembranous/enzymology , Enterocolitis, Pseudomembranous/microbiology , Epidermal Growth Factor/administration & dosage , Ileum/enzymology , Ileum/microbiology , Lactobacillus acidophilus/growth & development , Mice , Mice, Inbred BALB C , Peroxidase/metabolism , Probiotics/administration & dosage
4.
Article in English | IMSEAR | ID: sea-37375

ABSTRACT

Globally, colorectal cancer is the third commonest cancer in men since 1975.The present study focuses on the preventive strategies aimed at reducing the incidences and mortality of large bowel cancer. Chemoprevention of colon cancer appears to be a very realistic possibility because various intermediate stages have been identified preceding the development of malignant colonic tumors. Several studies have demonstrated that generous consumption of vegetables reduces the risk of colon cancer. This idea has prompted the present investigation to search for some novel plant products, which may have possible anticarcinogenic activity. It has already been proved from various experiments that chemopreventive agents, by virtue of their anti-oxidant, anti-inflammatory, anti-proliferative, apoptosis-inducing activity, act at various levels including molecular, cellular, tissue and organ levels to interfere with carcinogens. Previous studies from our laboratory have already reported the inhibitory effect of cinnamon and cardamom on azoxymethane induced colon carcinogenesis by virtue of their anti-inflammatory, anti-proliferative and pro-apoptotic activity. This particular experiment was carried out to assess the anti-oxidative potential of these spices. Aqueous suspensions of cinnamon and cardamom have been shown to enhance the level of detoxifying enzyme (GST activity) with simultaneous decrease in lipid peroxidation levels in the treatment groups when compared to that of the carcinogen control group.


Subject(s)
Animals , Azoxymethane/toxicity , Carcinogens/toxicity , Cinnamomum zeylanicum , Colon/enzymology , Colonic Neoplasms/chemically induced , Elettaria , Glutathione Transferase/metabolism , Lipid Peroxidation/drug effects , Liver/enzymology , Mice , Phytotherapy , Precancerous Conditions/chemically induced
5.
The Korean Journal of Gastroenterology ; : 335-339, 2005.
Article in Korean | WPRIM | ID: wpr-118712

ABSTRACT

BACKGROUND/AIMS: Ischemic colitis is a vascular condition of inadequate blood flow in the colon which leads to colonic inflammation and can cause significant morbidity and mortality. Oxidative stress is an early initiating event in ischemia and reperfusion injury. Heme oxygenase (HO) is considered to be an antioxidant enzyme that catabolizes heme to carbon monoxide, free iron and biliverdin. The aim of this study was to evaluate the expression patterns of HO-1, inducible form of HO, in ischemic colitis. METHODS: We analyzed the twelve cases of clinically and pathologically diagnosed ischemic colitis without surgical intervention compared with normal colon (n=10) and psedomembranous colitis (n=5). Immunohistochemical stainings for HO-1 were performed in paraffin-embedded tissues. RESULTS: The age of the patients ranged from 56 to 84 years (mean: 67 years) in ischemic colitis. Eight patients (66.7%) were female. The most common presenting symptom was bloody stool (66.7%) and rectosigmoid area (91.7%) of the large intestine was the most common ischemic site. Expression of HO-1 in ischemic colitis was high in contrast to normal colonic mucosa or psedomembranous colitis. CONCLUSIONS: Ischemic colitis usually involves the rectosigmoid area in elderly female patients with a history of bloody stool. High expression of HO-1 in ischemic colitis may be responsible for a protective mechanism to ischemia or heme injury.


Subject(s)
Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Colitis, Ischemic/enzymology , Colon/enzymology , Heme Oxygenase (Decyclizing)/metabolism , Immunohistochemistry , Intestinal Mucosa/enzymology
6.
The Korean Journal of Gastroenterology ; : 308-313, 2004.
Article in Korean | WPRIM | ID: wpr-92187

ABSTRACT

BACKGROUND/AIMS: Inflammation-induced alterations in smooth muscle contractility may be due to the effects on smooth muscle itself, neurotransmitters or enteric nerves. In dextran sulfate sodium-induced colitic rat, the delay in colonic transit was caused by decreased activity and production of neuronal nitric oxide synthase (nNOS) in the myenteric plexus of the distal colon. The aim of this study was to investigate the relationship between the delay in colonic transit and the distribution of inducible NOS (iNOS) and nNOS immunoreactive cells in the myenteric plexus of trinitrobenzene sulfonic acid (TNBS)-induced colitic guinea pig. METHODS: Sacrificed and their colonic tissues of forty-five TNBS-induced colitic guinea pigs were used to measure the colonic transit, and analyzed by immunohistochemistry. RESULTS: Colonic transit was delayed significantly at 3, 7 and 14 days after administration of TNBS. In control, nNOS immunoreactivity was present in the mucosa, submucosa, lamina propria, and ganglion cells of the myenteric plexus, while after TNBS treatment, reduced nNOS cells were found. However, the number of nNOS ganglion cells in the myenteric plexus was similar to those seen in controls. After administration of TNBS, iNOS immunoreactivity was increased in the mucosa and submucosa, but the number of iNOS positive ganglion cells in the myenteric plexus was not changed compared to control. CONCLUSIONS: It is suggested that in TNBS-induced guinea pig colitis, delayed colonic transit is not associated with the expression of nNOS nor iNOS in the myenteric plexus.


Subject(s)
Animals , Male , Colitis/chemically induced , Colon/enzymology , English Abstract , Gastrointestinal Transit , Guinea Pigs , Myenteric Plexus/enzymology , Nitric Oxide Synthase/metabolism , Trinitrobenzenesulfonic Acid
7.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 152-4, 2002.
Article in English | WPRIM | ID: wpr-634044

ABSTRACT

In order to investigate the relationship between the expression of heme oxygenase-2 (HO-2) mRNA and the pathogenesis of Hirschsprung's disease (HD), total ribonucleic acid (RNA) was extracted in the aganglionic and ganglionic segments of colon respectively from 15 cases of HD. The single-stranded cDNA of HO-2 was synthesized and further amplified by reverse transcription-polymerase chain reaction (RT-PCR). The expression of HO-2 mRNA was normal in ganglionic segments, but absent in aganglionic segments. It is concluded that the absence of HO-2 mRNA expression may be an important mechanism responsible for HD.


Subject(s)
Colon/enzymology , Heme Oxygenase (Decyclizing)/biosynthesis , Heme Oxygenase (Decyclizing)/genetics , Hirschsprung Disease/enzymology , Hirschsprung Disease/etiology , Hirschsprung Disease/genetics , RNA, Messenger/biosynthesis , RNA, Messenger/genetics
8.
Braz. j. med. biol. res ; 20(6): 697-702, 1987. tab
Article in English | LILACS | ID: lil-77418

ABSTRACT

1. The activity of choline acetyltransferase (CAT) measured by a radilabeling method was significantly reduced in the heart, submandibular gland and esophagus of rats 20 days after inoculation with Trypanosoma cruzi (Y strain). 2. Normal enzyme activity was recovered in all these organs 100 days after inoculation. 3. In the transcerse colon, no change, 30% reduction and normal activity were found at days 20, 100 and 430 of infection, respectively. 4. The data indicate recovery of parasympathetic function in experimental Chagas' disease. Axonal regrowth and sprouting are discussed as possible candidates for the recovery mechanisms


Subject(s)
Rats , Animals , Male , Female , Chagas Disease/enzymology , Choline O-Acetyltransferase/metabolism , Esophagus/enzymology , Submandibular Gland/enzymology , Myocardium/enzymology , Parasympathetic Nervous System/physiopathology , Colon/enzymology , Nerve Regeneration , Neuronal Plasticity , Neurons/physiology , Rats, Inbred Strains
SELECTION OF CITATIONS
SEARCH DETAIL