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Effects of cancer-induced cachexia and administration of l-glutathione on the intestinal mucosa in rat
in
Animal models
/ Apoptosis
/ Atrophy
/ Cachexia
/ Cancer
/ Cell proliferation
/ Damage assessment
/ Damage detection
/ Duodenum
/ Gastrointestinal system
/ Gastrointestinal tract
/ Glutathione
/ Goblet cells
/ Intestine
/ Mast cells
/ Morphometry
/ Mucosa
/ Oxidative stress
/ Tumors
/ Vasoactive agents
/ Vasoactive intestinal peptide
2024
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Effects of cancer-induced cachexia and administration of l-glutathione on the intestinal mucosa in rat
by
in
Animal models
/ Apoptosis
/ Atrophy
/ Cachexia
/ Cancer
/ Cell proliferation
/ Damage assessment
/ Damage detection
/ Duodenum
/ Gastrointestinal system
/ Gastrointestinal tract
/ Glutathione
/ Goblet cells
/ Intestine
/ Mast cells
/ Morphometry
/ Mucosa
/ Oxidative stress
/ Tumors
/ Vasoactive agents
/ Vasoactive intestinal peptide
2024
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Effects of cancer-induced cachexia and administration of l-glutathione on the intestinal mucosa in rat
in
Animal models
/ Apoptosis
/ Atrophy
/ Cachexia
/ Cancer
/ Cell proliferation
/ Damage assessment
/ Damage detection
/ Duodenum
/ Gastrointestinal system
/ Gastrointestinal tract
/ Glutathione
/ Goblet cells
/ Intestine
/ Mast cells
/ Morphometry
/ Mucosa
/ Oxidative stress
/ Tumors
/ Vasoactive agents
/ Vasoactive intestinal peptide
2024
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Effects of cancer-induced cachexia and administration of l-glutathione on the intestinal mucosa in rat
Journal Article
Effects of cancer-induced cachexia and administration of l-glutathione on the intestinal mucosa in rat
2024
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Overview
Walker-256 tumor is an experimental model known to promote cachexia syndrome, oxidative stress, and systemic inflammation. This study evaluated the duodenal mucosa of rats with Walker-256 tumor administered with 1% l-glutathione, intending to evaluate the damage caused by cancer-associated cachexia in the gastrointestinal tract and the effects of antioxidant administration on mucosal protection. Twenty-four 55-day-old male Wistar rats were distributed into four groups: control (C); control administered with 1% l-glutathione (C-GSH); Walker-256 tumor (W) and Walker-256 tumor administered with 1% l-glutathione (W-GSH). After 14 days of treatment, the duodenum was harvested for morphometric analysis of the mucosa, proliferation, apoptosis, immunostaining of varicosities immunoreactive (IR) to vasoactive intestinal peptide (VIP) and 5-HT-IR cells, and quantification of mast cells and goblet cells. Walker-256 tumor-bearing rats showed cachexia syndrome, mucosal atrophy, reduced cell proliferation, reduced 5-HT-IR cells, and increased goblet cells and VIPergic varicosities, which were not reversed by l-glutathione. On the other hand, l-glutathione caused a reduction of cells in apoptosis and mast cell recruitment, demonstrating a partial recovery of the damage detected in the intestinal mucosa.
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