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1.
Animal ; : 1-9, 2018 Dec 18.
Article in English | MEDLINE | ID: mdl-30560755

ABSTRACT

The rapid shift to high-grain (HG) diets in ruminants can affect the function of the rumen epithelium, but the dynamic changes in the composition of the epithelium-associated (epimural) bacterial community in sheep still needs further investigation. Twenty male lambs were randomly allocated to four groups (n = 5). Animals of the first group received hay diet and represented a control group (CON). Simultaneously, animals in the other three groups (HG groups) were rapidly shifted to an HG diet (60% concentrate)which continued for 7 (HG7), 14 (HG14) and 28 (HG28) days, correspondingly. Results showed that ruminal pH dramatically decreased due to the rapid shift to the HG diet (P <0.001), while, the concentrations of butyrate (P <0.001), lactate (P = 0.001), valerate (P = 0.008) and total volatile fatty acids (P = 0.001) increased. Diversity estimators showed a dramatic decrease after the shift without recovering as the HG feeding continued. The principal coordinates analysis showed that CON group clustered separately from all HG groups with the presence of significant difference only between HG7 and HG28 (P = 0.034). The non-parametric multivariate analysis (npmv R-package) deduced that the primary significant differences in phyla and phylogenetic investigation of communities by reconstruction of unobserved states (PICRUSt)-predicted Kyoto Encyclopedia of Genes and Genomes (KEGGs) was attributed mainly to the diet composition (P <0.001, P = 0.001) compared to its application period (P = 0.140, 0.545) which showed a significant effect only on the genus (P = 0.001) and the operational taxonomic units (OTUs) level (P = 0.011). The Kruskal-Wallis test deduced that six phyla showed a significant effect due to the shift in diet composition. At the genus level, HG feeding altered the abundance of 12 taxa, four of which showed a significant variation due to the duration of the HG diet application. Similarly, we found that 21 OTUs showed significant variations due to the duration of the HG diet application. Furthermore, the genes abundance predicted by PICRUSt revealed that the HG feeding significantly affected seven metabolic pathways identified in the KEGG. Particularly, the abundance of gene families associated with carbohydrates metabolism were significantly higher in HG feeding groups (P = 0.027). Collectively, these results revealed that the rapid transition to an HG diet causes dramatic alterations in ruminal fermentation and the composition and function of ruminal epithelium-associated microbiome in sheep, while, the duration of the HG diet application causes drastic alterations to the abundance of some species.

2.
Ann Pharm Fr ; 71(2): 119-22, 2013 Mar.
Article in French | MEDLINE | ID: mdl-23537413

ABSTRACT

Whether intestinal toxicity of preferential or selective COX-2 inhibitors is reduced compared with that of standard NSAIDs is controversial. A 26-year-old woman presented with acute abdominal pain and bloody diarrhoea a few days after beginning meloxicam treatment. Endoscopic examination of the colon showed erythematous and ulcerative lesions involving 15 cm of the left colon. No aetiology has been found for colitis. Diarrhea disappeared 1 week after meloxicam was stopped. Total colonoscopy 3 months and 2 years later was normal. The role of meloxicam in the etiology of colitis was considered plausible. This report and a few other cases in the literature suggest that cyclooxygenase-2 selective non-steroidal anti-inflammatory drug inhibitor toxicity should be investigated in case of unexplained acute colitis.


Subject(s)
Abdominal Pain/etiology , Colitis/chemically induced , Cyclooxygenase 2 Inhibitors/adverse effects , Thiazines/adverse effects , Thiazoles/adverse effects , Abdominal Pain/diagnostic imaging , Adult , Analgesics, Non-Narcotic/therapeutic use , Colitis/complications , Colitis/diagnostic imaging , Colonoscopy , Female , Humans , Meloxicam , Nefopam/therapeutic use , Tomography, X-Ray Computed
4.
Ann Pharm Fr ; 69(6): 302-5, 2011 Nov.
Article in French | MEDLINE | ID: mdl-22115133

ABSTRACT

Iron deficiency anemia as a hematologic complication of the antithyroid medication (ATS) that has not been already described in the literature. We report on two exceptional cases: the first case concerns a 24 years old man admitted for an anemic syndrome. He was treated with carbimazole for Graves' disease. The blood count showed a non-regenerative microcytic anemia. Serum ferritin was severely decreased. The etiologic searching for bleeding, hemolysis, malabsorption or iron deficiency was negative. Treatment with iron salts was introduced without any real improvement. Given this situation, and given the negativity of the etiologic investigations, the decision to stop carbimazole was taken. Since that, the clinical and biological evolutions have been favorable. The second observation is much more original and concerns a 35 years old woman. The clinical, laboratory, etiological and treatment data are similar to those of the first observation. The evolution after withdrawal of carbimazole was favorable. The originality of this observation is that a reintroduction test of carbimazole was performed and allowed to reproduce the same haematological effects. These findings led us to hold the diagnosis of anaemia due to carbimazole. In this occasion, and in the light of the data in the literature, we underline the exceptional character of these two cases and we raise the possibility of an etiopathogenic link between administration of ATS and the occurrence of anaemia by iron deficiency.


Subject(s)
Anemia, Iron-Deficiency/chemically induced , Antithyroid Agents/adverse effects , Carbimazole/adverse effects , Adult , Antithyroid Agents/therapeutic use , Blood Chemical Analysis , Carbimazole/therapeutic use , Female , Ferritins/blood , Graves Disease/complications , Graves Disease/drug therapy , Humans , Iron Compounds/therapeutic use , Male , Young Adult
5.
Ann Burns Fire Disasters ; 24(3): 157-9, 2011 Sep 30.
Article in French | MEDLINE | ID: mdl-22396676

ABSTRACT

The Ogilvie syndrome is an acute colonic dilatation of the previously healthy colon, without any organic obstruction. Pathological circumstances such as burns and antipsychotic medication have been identified as predisposing elements. The incidence of this complication, in the reanimation of burn patients, varies between 0.5 to 1%. The purpose of our study is to draw attention to the Ogilvie symptom by describing a case with its clinical and paraclinical data, its physiopathological causes, and the therapeutic aspects. The clinical picture in our patient was characteristic: extensive abdominal meteorism. The abdominal scan showed massive colonic dilatation without any mechanical obstacles. The outcome was successful after colonoscopic exsufflation. The Ogilvie syndrome is a rare occurrence which without effective treatment may result in caecal perforation and a poor prognosis. It is therefore necessary to establish the diagnosis early and, in particular, to initiate close radiological follow-up after the establishment of medical treatment, in which colonoscopy plays an important part.

6.
Transfus Clin Biol ; 16(1): 39-42, 2009 Mar.
Article in French | MEDLINE | ID: mdl-19329346

ABSTRACT

INTRODUCTION: The liver and central nervous system are the usual targets of Wilson's disease, an inherited disorder of copper metabolism. Severe hemolytic anemia is an unusual complication of Wilson's disease. EXEGESIS: We report a case of Wilson's disease revealed by acute intravascular repeating hemolytic anemia associated with liver failure. The initially negative etiologic investigation was directed by occurred of liver failure. The genetic study allowed to discover an other similar case. The evolution was favourable under treatment with zinc sulfate and penicillamine. DISCUSSION: Diagnosis of Wilson's disease must be considered in case of acute hemolytic anemia associated with liver failure in young adults.


Subject(s)
Anemia, Hemolytic/etiology , Hepatolenticular Degeneration/diagnosis , Acute Disease , Arrhythmias, Cardiac/etiology , Chelating Agents/therapeutic use , Chelation Therapy , Child , Consanguinity , Copper , Dyspnea/etiology , Female , Hepatolenticular Degeneration/complications , Hepatolenticular Degeneration/drug therapy , Hepatolenticular Degeneration/genetics , Humans , Jaundice, Obstructive/etiology , Liver Failure/etiology , Male , Penicillamine/therapeutic use , Recurrence , Young Adult , Zinc Sulfate/therapeutic use
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