CONTEXT: Only a few studies evaluated the digestive alterations caused by low frequency noise (LFN) and most focused only on mucosal alterations. OBJECTIVES: To investigate the morphological injury of LFN-exposed gastric wall, beyond the epithelial layer. METHODS: Wistar rats were exposed to low frequency noise (LFN), during increasing periods, 1 to 13 weeks. A control group was kept in silence. Gastric specimens were studied using: (i) light microscopy with hematoxylin-eosin and immunostaining for collagens; (ii) transmission electron microscopy; (iii) morphometry allowing statistical analysis. RESULTS: Submucosa of all LFN-exposed animals exhibit increased thickness with fibrous proliferation. Transmission electron microscopy showed massive collagen deposition. Immunostaining identified collagen IV as responsible for the increased thickness. Morphometry allowed the demonstration of a significant difference of thickness between control and exposed groups. Vascular alterations included: i) intima proliferation and thickening, rupture of the internal elastic lamina, thrombotic changes; ii) thickening of the media; iii) after 9 weeks of LFN-exposure, we found new formed vessel presenting tortuous and twisted. There is a significant difference of arterial wall thickness between control and exposed groups. CONCLUSIONS: Deeper layers of gastric wall undergo alterations, including fibrosis of the submucosa caused by collagen IV deposition, an early marker of neoangiogenesis. Vascular alterations included thickening and thrombotic phenomena, but also images of newly formed vessels. This study suggests that, at least in the stomach, LFN-induced fibrosis could be linked with neoangiogenesis.
CONTEXT: Only a few studies evaluated the digestive alterations caused by low frequency noise (LFN) and most focused only on mucosal alterations. OBJECTIVES: To investigate the morphological injury of LFN-exposed gastric wall, beyond the epithelial layer. METHODS:Wistar rats were exposed to low frequency noise (LFN), during increasing periods, 1 to 13 weeks. A control group was kept in silence. Gastric specimens were studied using: (i) light microscopy with hematoxylin-eosin and immunostaining for collagens; (ii) transmission electron microscopy; (iii) morphometry allowing statistical analysis. RESULTS: Submucosa of all LFN-exposed animals exhibit increased thickness with fibrous proliferation. Transmission electron microscopy showed massive collagen deposition. Immunostaining identified collagen IV as responsible for the increased thickness. Morphometry allowed the demonstration of a significant difference of thickness between control and exposed groups. Vascular alterations included: i) intima proliferation and thickening, rupture of the internal elastic lamina, thrombotic changes; ii) thickening of the media; iii) after 9 weeks of LFN-exposure, we found new formed vessel presenting tortuous and twisted. There is a significant difference of arterial wall thickness between control and exposed groups. CONCLUSIONS: Deeper layers of gastric wall undergo alterations, including fibrosis of the submucosa caused by collagen IV deposition, an early marker of neoangiogenesis. Vascular alterations included thickening and thrombotic phenomena, but also images of newly formed vessels. This study suggests that, at least in the stomach, LFN-induced fibrosis could be linked with neoangiogenesis.
Authors: Maria Alzira Cavacas; Vitor Tavares; Maria João Oliveira; Pedro Oliveira; Ana Sezinando; José Martins dos Santos Journal: Int J Clin Exp Pathol Date: 2013-11-15
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Authors: Maria Alzira Cavacas; Vitor Tavares; Gonçalo Borrecho; Maria João Oliveira; Pedro Oliveira; José Brito; Artur Águas; José Martins Dos Santos Journal: Int J Med Sci Date: 2015-02-27 Impact factor: 3.738
Authors: Surya C Gnyawali; Kasturi G Barki; Shomita S Mathew-Steiner; Sriteja Dixith; Daniel Vanzant; Jayne Kim; Jennifer L Dickerson; Soma Datta; Heather Powell; Sashwati Roy; Valerie Bergdall; Chandan K Sen Journal: PLoS One Date: 2015-03-23 Impact factor: 3.240
Authors: José João Baltazar Mendes; Pedro Miguel Antunes Oliveira; José Américo Almeida de Brito; Artur Manuel Perez Neves Águas; José António Mesquita Martins Dos Santos Journal: J Indian Soc Periodontol Date: 2014-07