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      Biodistribution of the radiophamarceutical sodium pertechnetate (Na99mTcO4) after massive small bowel resection in rats Translated title: Biodistribuição do radiofármaco pertecnetato de sódio (Na99mTcO4) em ratos submetidos a ressecção extensa de intestino delgado

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          Abstract

          PURPOSE: To evaluate the biodistribution of sodium pertecnetate (Na99mTcO4) in organs and tissues, the morphometry of remnant intestinal mucosa and ponderal evolution in rats subjected to massive resection of the small intestine. METHODS: Twenty-one Wistar rats were randomly divided into three groups of 7 animals each. The short bowel (SB) group was subjected to massive resection of the small intestine; the control group (C) rats were not operated on, and soft intestinal handling was performed in sham rats. The animals were weighed weekly. On the 30th postoperative day, 0.l mL of Na99mTcO4, with mean activity of 0.66 MBq was injected intravenously into the orbital plexus. After 30 minutes, the rats were killed with an overdose of anesthetic, and fragments of the liver, spleen, pancreas, stomach, duodenum, small intestine, thyroid, lung, heart, kidney, bladder, muscle, femur and brain were harvested. The biopsies were washed with 0.9% NaCl.,The radioactivity was counted using Gama Counter WizardTM 1470, PerkinElmer. The percentage of radioactivity per gram of tissue (%ATI/g) was calculated. Biopsies of the remaining jejunum were analysed by HE staining to obtain mucosal thickness. Analysis of variance (ANOVA) and the Tukey test for multiple comparisons were used, considering p<0.05 as significant. RESULTS: There were no significant differences in %ATI/g of the Na99mTcO4 in the organs of the groups studied (p>0.05). An increase in the weight of the SB rats was observed after the second postoperative week. The jejunal mucosal thickness of the SB rats was significantly greater than that of C and sham rats (p<0.05). CONCLUSION: In rats with experimentally-produced short bowel syndrome, an adaptive response by the intestinal mucosa reduced weight loss. The biodistribution of Na99mTcO4 was not affected by massive intestinal resection, suggesting that short bowel syndrome is not the cause of misleading interpretation, if an examination using this radiopharmaceutical is indicated.

          Translated abstract

          OBJETIVO: Avaliar em modelo animal com ressecção extensa do intestino delgado a biodistribuição de pertecnetato de sódio (Na99mTcO4) em órgãos e tecidos, a evolução ponderal e a morfometria da mucosa do intestino delgado remanescente. MÉTODOS: Vinte e um ratos Wistar foram aleatoriamente divididos em três grupos de sete animais cada. O grupo intestino curto (IC) foi submetido a ressecção extensa do intestino delgado, o grupo controle (C) não foi operado e o grupo sham foi submetido a leve manipulação cirúrgica das alças intestinais.Todos foram pesados semanalmente. No 30º dia pós-operatório foi administrado 0,l mL de Na99mTcO4 aos animais dos três grupos, IV no plexo orbital, com atividade radioativa média de 0,66MBq. Após 30 minutos os ratos foram mortos e retirados fragmentos do fígado, baço, pâncreas, estomago, duodeno, intestino delgado, tireóide, pulmão, coração, rim, bexiga, músculo, fêmur, e cérebro. As amostras foram lavadas com solução de NaCl 0,9%.A radioatividade foi contada peloContador Gama 1470, WizardTM Perkin-Elmer e calculado o percentual de atividade radioativa por grama (%ATI/g) de cada órgão. Biópsias do jejuno foram submetidas a análise da espessura da mucosa (coloração HE). Utilizou-se avaliação estatística paramétrica (ANOVA) e teste de Tukey, considerando p<0,05 como significante. RESULTADOS: Não houve diferenças significantes da %ATI/g nos órgãos dos grupos estudados (p>0,05). Verificou-se acentuada redução inicial de peso, em seguida um aumento do peso dos animais tratados a partir da segunda semana de observação e aumento da espessura da mucosa jejunal do grupo IC, comparado com os demais. CONCLUSÃO: Em ratos com síndrome do intestino curto, uma adaptação na espessura da mucosa contribuiu para reversão na perda de peso inicial e para que a biodistribuição do Na99mTcO4 não fosse afetada pela ressecção extensa do intestino, sugerindo que o intestino curto não é causa de interpretações duvidosas, quando exame cintilográfico com este radiofármaco estiver indicado.

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          Most cited references26

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          Intestinal loop lengthening--a technique for increasing small intestinal length.

          A reproducible technique is described for doubling the length of a loop of small intestine, while simultaneously reducing its luminal diameter, and preserving the maximum amount of small bowel mucosa for intestinal adaptation. In pig experiments, 7 loops have been increased in length by the "intestinal loop lengthening" procedure, with survival of 5 of the 7 animals for a period of 16-26 wk. Leakage from the lengthened intestinal segment led to the death of one animal. At a second operation, or at termination of the experiment, all seven lengthened loops had a good blood supply and were patent along their full length. Histologic examination of 3 of the 4 specimens from the first phase of the study confirmed their viability. The potential application of intestinal loop lengthening in the management of the short gut syndrome is discussed.
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            Induction of intestinal epithelial proliferation by glucagon-like peptide 2.

            Injury, inflammation, or resection of the small intestine results in severe compromise of intestinal function. Nevertheless, therapeutic strategies for enhancing growth and repair of the intestinal mucosal epithelium are currently not available. We demonstrate that nude mice bearing subcutaneous proglucagon-producing tumors exhibit marked proliferation of the small intestinal epithelium. The factor responsible for inducing intestinal proliferation was identified as glucagon-like peptide 2 (GLP-2), a 33-aa peptide with no previously ascribed biological function. GLP-2 stimulated crypt cell proliferation and consistently induced a marked increase in bowel weight and villus growth of the jejunum and ileum that was evident within 4 days after initiation of GLP-2 administration. These observations define a novel biological role for GLP-2 as an intestinal-derived peptide stimulator of small bowel epithelial proliferation.
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              Intestinal adaptation in short bowel syndrome.

              Regaining enteral autonomy after extensive small bowel resection is dependent on intestinal adaptation. This adaptational process is characterized by hyperplastic growth of the remaining gut, which is accompanied by both an increase of cell division at the level of the crypt cells and by an increased rate of programmed cell death (apoptosis). Apart from the absorptive function, the small bowel also has a barrier function and plays an important role in interorgan metabolism. Also, these functions are greatly affected by a massive intestinal resection and subsequent recovery by intestinal adaptation. This review aims to give an overview of the debilitating effects of massive intestinal resection on gut function and subsequently discusses intestinal adaptation and possible factors stimulating adaptation.
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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Journal
                acb
                Acta Cirurgica Brasileira
                Acta Cir. Bras.
                Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (São Paulo )
                1678-2674
                December 2007
                : 22
                : 6
                : 430-435
                Affiliations
                [1 ] Universidade Federal do Rio Grande do Norte Brazil
                [2 ] Universidade Federal do Rio Grande do Norte Brazil
                [3 ] Universidade Federal do Rio Grande do Norte Brazil
                [4 ] UERJ Brazil
                [5 ] Universidade Federal do Rio Grande do Norte Brazil
                Article
                S0102-86502007000600003
                10.1590/S0102-86502007000600003
                5239bc08-44d0-43c7-8b5d-96b8fbdfd145

                http://creativecommons.org/licenses/by/4.0/

                History
                Product

                SciELO Brazil

                Self URI (journal page): http://www.scielo.br/scielo.php?script=sci_serial&pid=0102-8650&lng=en
                Categories
                SURGERY

                Surgery
                Short Bowel Syndrome,Sodium Pertechnetate Tc 99m,Pharmacokinetics,Rat,Síndrome do Intestino Curto,Pertecnetato Tc99m de Sódio,Farmacocinética,Ratos

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