Related Experiment Video
Updated: May 1, 2026

Analyzing Beneficial Effects of Nutritional Supplements on Intestinal Epithelial Barrier Functions During Experimental Colitis
Published on: January 5, 2017
Glutamine alleviates feed restriction-induced barrier function injury in yak rumen epithelium
Ziqi Yue1,2, Shanpeng Ke1,2, Ali Mujtaba Shah2,3
1Animal Nutrition Institute, Sichuan Agricultural University, Chengdu 611130, China.
Abstract:
The yak (Bos grunniens) is a crucial species for herders on the Qinghai-Tibet Plateau. Cold-season forage scarcity often leads to starvation, impairing the rumen epithelial barrier function and growth performance. Glutamine (Gln) has been shown to mitigate injury to the gastrointestinal tract barrier function, but its efficacy and mechanism against feed restriction (FR)-induced barrier injury in yaks remains unclear. This study combined in vivo and in vitro experiments to investigate this. Twenty-four healthy yaks (31 months, 265.35 ± 25.81 kg) were randomly divided into three groups (n = 8 per group) and fed for 60 d : the control (Con, ad libitum access to the basal diet), FR (50% of the basal diet), and FR + Gln (50% of the basal diet in the first month, with 1% Gln added to the 50% basal diet in the second month). Yak rumen epithelial cells (YRECs) were treated under four conditions: Control (normal medium), Gln (normal medium + 10 mmol/L Gln), Gln deficiency (Gln-D, Gln-free medium), and Gln-D + Gln (Gln-free medium + 10 mmol/L Gln). Results showed that FR significantly decreased the average daily gain (ADG) and the Gln concentration in ruminal epithelial tissue and serum (P < 0.05) and increased serum levels of permeability parameters (diamine oxidase, D-lactate, lipopolysaccharide, and histamine) compared to the Con group (P < 0.05). In addition, FR in vivo or Gln-D in vitro significantly down-regulated the protein expression of tight junction (TJ) proteins (ZO-1, occludin, and claudin-1) (P < 0.05) and enhanced the phosphorylation of nuclear factor-κB p65 (NF-κB p65), p38 mitogen-activated protein kinase (p38 MAPK), and c-junN-terminal kinase (JNK) (P < 0.05). Gln supplementation effectively reversed these changes, significantly reducing serum permeability (P < 0.001), restoring TJ protein expression, and suppressing the phosphorylation of NF-κB p65, p38 MAPK, and JNK compared to the FR or Gln-D groups (P < 0.01). Crucially, the ability of Gln to restore TJ integrity was abolished by p38 MAPK and JNK activators in YRECs (P < 0.001). Overall, this suggests that dietary Gln supplementation alleviates FR-induced rumen epithelial barrier damage in yaks through the MAPK/NF-κB pathway.
More Related Videos
08:07Author Spotlight: Isolation and Characterization of Equine Submucosal Enteric Glia — Implications for Preventing Postoperative Complications in Colic Surgery
Published on: October 4, 2024
08:37Assessment of Glutamine as a Fuel Source for Alveolar Macrophages Exposed to Chronic Ethanol Using an Extracellular Flux Bioanalyzer
Published on: November 15, 2024
Related Concept Videos
Protein Digestion
Therapeutic Index
Vitamins
Gastritis III: Clinical Manifestations and Management
Clinical manifestations of acute gastritis
The patient with acute gastritis may have a rapid onset of symptoms, such as epigastric pain or discomfort, dyspepsia, anorexia, hiccups, or nausea and vomiting, which can last from a few hours to a few days. Erosive or hemorrhagic gastritis may cause bleeding, which may manifest as blood in vomit or as...
Dipeptidyl Peptidase 4 Inhibitors
Myocarditis III: Medical Management