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  1. Article ; Online: L-glutamine supplementation reduced morphological damage in the renal glomerulus of rats with Walker-256 tumor.

    Lima, Kaio Ramon de Aguiar / Lopes, Maria Luiza Diniz de Sousa / Souza, Sara Raquel Garcia de / Fracaro, Luciane / Purificação, Natan Reyges Castro da / Lima, Marília Fabiana de Oliveira / Lins, Lucas Alexandre Araújo / Lacchini, Silvia / Araújo, Aurigena Antunes de / Araújo Júnior, Raimundo Fernandes de / Perles, Juliana Vanessa Colombo Martins / Zanoni, Jacqueline Nelisis / Clebis, Naianne Kelly

    Acta cirurgica brasileira

    2023  Volume 38, Page(s) e383923

    Abstract: Purpose: To evaluate the effects of the experimental subcutaneous Walker-256 tumor and L-glutamine supplementation, an antioxidant, on the glomerular morphology of rats.: Methods: Twenty Wistar rats were distributed into four groups (n = 5): control ( ...

    Abstract Purpose: To evaluate the effects of the experimental subcutaneous Walker-256 tumor and L-glutamine supplementation, an antioxidant, on the glomerular morphology of rats.
    Methods: Twenty Wistar rats were distributed into four groups (n = 5): control (C); control treated with 2% L-glutamine (CG); rats with Walker-256 tumor (WT); and rats with Walker-256 tumor treated with 2% L-glutamine (WTG). Renal histological samples were submitted to periodic acid-Schiff and Masson's Trichrome staining to analyze glomerular density, morphometry of glomerular components and glomerulosclerosis; and to immunohistochemistry for fibroblast growth factor-2 (FGF-2).
    Results: WT showed 50% reduction in body mass gain and cachexia index > 10%, while WTG demonstrated reduction in cachexia (p < 0.05). WT revealed reduction of glomerular density, increase in the glomerular tuft area, mesangial area, matrix in the glomerular tuft, decrease in the urinary space and synechia, and consequently higher glomerulosclerosis (p < 0.05). L-glutamine supplementation in the WTG improved glomerular density, and reduced glomerular tuft area, urinary space, mesangial area, and glomerulosclerosis compared to WT(p < 0.05). WT showed higher collagen area and FGF-2 expression compared to C (p < 0.05). WTG presented lower collagen fibers and FGF-2 expression compared to WT (p < 0.05).
    Conclusions: L-glutamine supplementation reduced cachexia and was beneficial for glomerular morphology of the rats, as well as it reduced kidney damage and improved the remaining glomeruli morphology.
    MeSH term(s) Rats ; Animals ; Rats, Wistar ; Glutamine/pharmacology ; Cachexia/metabolism ; Cachexia/pathology ; Fibroblast Growth Factor 2 ; Neoplasms ; Dietary Supplements ; Collagen
    Chemical Substances Glutamine (0RH81L854J) ; Fibroblast Growth Factor 2 (103107-01-3) ; Collagen (9007-34-5)
    Language English
    Publishing date 2023-10-13
    Publishing country Brazil
    Document type Journal Article
    ZDB-ID 2012156-8
    ISSN 1678-2674 ; 1678-2674
    ISSN (online) 1678-2674
    ISSN 1678-2674
    DOI 10.1590/acb383923
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: QUERCETIN SUPPLEMENTATION PREVENTS CHANGES IN THE SEROTONIN AND CASPASE-3 IMMUNOREACTIVE CELLS OF THE JEJUNUM OF DIABETIC RATS.

    Martins-Perles, Juliana Vanessa Colombo / Zignani, Isabela / Souza, Sara Raquel Garcia de / Frez, Flávia Cristina Vieira / Bossolani, Gleison Daion Piovezana / Zanoni, Jacqueline Nelisis

    Arquivos de gastroenterologia

    2019  Volume 56, Issue 4, Page(s) 405–411

    Abstract: Background: Serotonin (5-HT) is present in the epithelial enterochromaffin cells (EC), mast cells of the lamina propria and enteric neurons. The 5-HT is involved in regulating motility, secretion, gut sensation, immune system and inflammation.: ... ...

    Abstract Background: Serotonin (5-HT) is present in the epithelial enterochromaffin cells (EC), mast cells of the lamina propria and enteric neurons. The 5-HT is involved in regulating motility, secretion, gut sensation, immune system and inflammation.
    Objective: Evaluate the effects of diabetes and quercetin supplementation on serotoninergic cells and its cell loss by apoptosis in jejunal mucosa of streptozotocin-induced diabetic rats (STZ-rats).
    Methods: Twenty-four male Wistar rats were divided into four groups: normoglycemic (C), normoglycemic supplemented with 40 mg/day quercetin (Q), diabetic (D) and diabetic supplemented with 40 mg/day quercetin (DQ). After 120 days, the jejunum was collected and fixated in Zamboni's solution for 18 h. After obtaining cryosections, immunohistochemistry was performed to label 5-HT and caspase-3. Quantification of 5-HT and caspase-3 immunoreactive (IR) cells in the lamina propria, villi and crypts were performed.
    Results: The diabetic condition displayed an increase of the number of 5-HT-IR cells in villi and crypts, while decreased number of these cells was observed in lamina propria in the jejunum of STZ-rats. In the diabetic animals, an increased density of apoptotic cells in epithelial villi and crypts of the jejunum was observed, whereas a decreased number of caspase-3-IR cells was observed in lamina propria. Possibly, quercetin supplementation slightly suppressed the apoptosis phenomena in the epithelial villi and crypts of the STZ-rats, however the opposite effect was observed on the 5-HT-IR cells of the lamina propria. Quercetin supplementation on healthy animals promoted few changes of serotoninergic function and apoptotic stimuli.
    Conclusion: These results suggest that quercetin supplementation mostly improved the serotonergic function affected by diabetes maybe due to antioxidant and anti-inflammatory properties of quercetin.
    MeSH term(s) Animals ; Antioxidants/administration & dosage ; Apoptosis/drug effects ; Caspase 3/metabolism ; Diabetes Mellitus, Experimental/drug therapy ; Diabetes Mellitus, Experimental/pathology ; Dietary Supplements ; Immunohistochemistry ; Interstitial Cells of Cajal/drug effects ; Interstitial Cells of Cajal/pathology ; Intestinal Mucosa/drug effects ; Jejunum/drug effects ; Jejunum/pathology ; Male ; Quercetin/administration & dosage ; Rats ; Rats, Wistar ; Serotonin/metabolism
    Chemical Substances Antioxidants ; Serotonin (333DO1RDJY) ; Quercetin (9IKM0I5T1E) ; Caspase 3 (EC 3.4.22.-)
    Language English
    Publishing date 2019-11-28
    Publishing country Brazil
    Document type Journal Article
    ZDB-ID 137743-7
    ISSN 1678-4219 ; 0004-2803
    ISSN (online) 1678-4219
    ISSN 0004-2803
    DOI 10.1590/S0004-2803.201900000-81
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Enteric innervation combined with proteomics for the evaluation of the effects of chronic fluoride exposure on the duodenum of rats.

    Melo, Carina Guimarães de Souza / Perles, Juliana Vanessa Colombo Martins / Zanoni, Jacqueline Nelisis / Souza, Sara Raquel Garcia de / Santos, Erika Xavier / Leite, Aline de Lima / Heubel, Alessandro Domingues / E Souza, Camila Oliveira / Souza, Juliana Gadelha de / Buzalaf, Marília Afonso Rabelo

    Scientific reports

    2017  Volume 7, Issue 1, Page(s) 1070

    Abstract: Ingested fluoride (F) is absorbed mainly in the small intestine, which is controlled by the Enteric Nervous System (ENS). Although important intestinal symptomatology has been described after excessive F exposure, there have been no studies reporting the ...

    Abstract Ingested fluoride (F) is absorbed mainly in the small intestine, which is controlled by the Enteric Nervous System (ENS). Although important intestinal symptomatology has been described after excessive F exposure, there have been no studies reporting the effects of F on the ENS. In this study, the effects of chronic F exposure were evaluated on the duodenums of rats through proteomic and morphological analyses. Concentrations of 0, 10, or 50 ppm of F were applied to the drinking water for 30 days. Immunofluorescence techniques were performed in the myenteric plexus of the duodenum to detect HuC/D, neuronal nitric oxide (nNOS), vasoactive intestinal peptide (VIP), calcitonin gene related peptide (CGRP), and substance P (SP). The 50 ppm F group presented a significant decrease in the density of nNOS-IR neurons. Significant morphological alterations were also observed in HUC/D-IR and nNOS-IR neurons; VIP-IR, CGRP-IR, and SP-IR varicosities for both groups (10 and 50 ppm F). Proteomic analysis of the duodenum demonstrated alterations in the expression of several proteins, especially those related to important biological processes, such as protein polymerization, which helps to explain the downregulation of many proteins upon exposure to 50 ppm of F.
    MeSH term(s) Administration, Oral ; Animals ; Cariostatic Agents/administration & dosage ; Cariostatic Agents/toxicity ; Duodenum/drug effects ; Duodenum/pathology ; Fluorescent Antibody Technique ; Fluorides/administration & dosage ; Fluorides/toxicity ; Nervous System/drug effects ; Nervous System/pathology ; Proteome/analysis ; Proteomics ; Rats
    Chemical Substances Cariostatic Agents ; Proteome ; Fluorides (Q80VPU408O)
    Language English
    Publishing date 2017-04-21
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-017-01090-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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