The negative impacts of stress on gastrointestinal tract (GIT) barrier function can result in compromised animal growth and health. Aspirin is known to cause mucosal injury leading to increased gut permeability and tight junction damage and can be used as a model to study leaky gut in cattle. The objective of this study was to determine the long-term impact of aspirin-induced chronic leaky gut on cattle growth and carcass attributes. Two treatments were evaluated in two studies: control (no aspirin) or 0.25% of the diet dry matter (DM) aspirin fed daily. Diets consisted of 50% corn, 24% dried distillers grains, 20% corn silage, and 6% supplement on a DM basis. In experiment 1, sixteen Angus × Simmental heifers, allotted by body weight (BW) and breed composition, were fed diets for 154 d. On day 155, heifers were dosed with 1 liter of a 180-mM Cr–ethylenediaminetetraacetic acid solution using an esophageal tube and had urine collected every 1.5 to 3 h for 48 h for analysis of Cr as a measure of gut leakiness. In experiment 2, ninety-six Simmental × Angus steers (355.0 ± 14.8 kg) were allotted by BW and breed composition and fed treatment diets for 159 d. Weight was recorded monthly and serum was collected on day 159 and analyzed for lipopolysaccharide-binding protein (LBP), interleukin-6 (IL-6), serum amyloid A (SAA), haptoglobin, and aspartate aminotransferase (AST). Data were analyzed using the MIXED procedure of SAS. Heifers fed 0.25% aspirin in experiment 1 excreted more Cr into urine compared with heifers not fed aspirin (overall treatment effect, P = 0.01). In experiment 2, aspirin tended to increase serum LBP (P = 0.06) but had no effect on concentrations of IL-6, haptoglobin, SAA, or AST (P ≥ 0.25). Aspirin tended to decrease average daily gain (P = 0.10), decreased hot carcass weight and rib-eye area (P ≤ 0.05), and increased fat thickness, marbling score, and yield grade (P ≤ 0.02). Aspirin tended to increase kidney, pelvic, and heart fat percentage (P = 0.10) and had no effect on liver abscesses (P ≥ 0.80). This study indicates that leaky gut induced by long-term administration of aspirin has negative impacts on feedlot performance and carcass composition. The negative impact of aspirin-induced leaky gut on animal performance suggests that chronic leaky gut caused by other factors (subacute acidosis, stress) may be a significant problem for the feedlot industry.
Stress negatively affects gastrointestinal tract (GIT) barrier function, resulting in compromised animal health. A deeper understanding of how diet and stress impacts GIT barrier function in feedlot cattle is needed. Aspirin decreases mucus production and mucosal repair in the GIT and could be used as a model for GIT barrier dysfunction research. The objective of this study was to evaluate the effectiveness of aspirin to induce GIT barrier dysfunction in beef cattle. In experiment 1, sixteen crossbred heifers (425.0 ± 8.6 kg) were allotted to 0, 50, 100, or 200 mg/kg BW aspirin doses based on BW. Experiment 1 consisted of 2 periods separated by 4 wks where 4 heifers per treatment received the same aspirin dose during each period. Heifers were fed a 49.4% corn silage, 50.6% concentrate diet. The 200 mg/kg BW aspirin treatment was dosed as a 100 mg/kg BW aspirin oral bolus 36 and 24 h prior to Cr-EDTA dosing (1 L; 180 mM). The 50 and 100 mg/kg BW aspirin treatments were dosed as an oral bolus 24 h prior to Cr-EDTA dosing. Urine was collected every 3 h for 48 h and analyzed for Cr. Serum was collected at 0 and 48 h and analyzed for lipopolysaccharide binding protein (LBP), interleukin-6 (IL-6), serum amyloid A (SAA), haptoglobin, and aspartate amino transferase (AST). In experiment 2, sixteen crossbred steers (576.0 ± 14.2 kg) fed a similar diet were allotted by BW to the 0 and 200 mg/kg BW aspirin treatments (8 steers/treatment) and were slaughtered 24 h after the last dose. Jejunal tissues were collected and claudin 1, 2 and 3, occludin, and zonula occludens tight junction mRNA expression was determined. Data were analyzed using the MIXED procedure of SAS. Urinary Cr excretion increased linearly at h 3, 6, 9, and 12 (P ≤0.04) as aspirin dose increased from 0 to 200 mg/kg. Aspirin linearly increased Cr absorption (P = 0.02) and elimination (P = 0.04) rates and linearly decreased mean retention time of Cr (P = 0.02). Aspirin increased SAA (P = 0.04) and tended to increase LBP (P = 0.09) in serum, but did not affect any other serum inflammatory marker (P ≥ 0.19). Aspirin tended to increase jejunal claudin-1 mRNA expression (P = 0.10), but did not affect mRNA expression of other genes regulating tight junction function (P ≥ 0.20). Results from this study indicate that aspirin disrupts GIT barrier function in beef cattle and has potential as a model in GIT permeability research.
Stress negatively effects gastrointestinal tract (GIT) barrier function, resulting in compromised animal health. The objective of this study was to evaluate the effectiveness of aspirin to intentionally induce GIT barrier dysfunction in beef cattle. In experiment 1, sixteen crossbred heifers (425 ± 8.6 kg) were enrolled in 2 experimental periods and allotted by BW to 0, 50, 100, or 200 mg/kg BW aspirin. Four heifers per treatment received the same aspirin dose during each period, which were separated by 4 wks. Heifers were fed a 49.4% corn silage, 50.6% concentrate diet. Aspirin was delivered to animals as an oral bolus. The 200 aspirin treatment was dosed as 100 mg/kg BW aspirin 36 and 24 h prior to Cr-EDTA dosing (1 L; 180 mM). The 50 and 100 aspirin treatments were dosed 24 h prior to Cr-EDTA dosing. Urine was collected every 3 h for 48 h and analyzed for Cr using atomic absorption spectrometry. Serum was collected at 0, 24, and 48 h and analyzed for lipopolysaccharide binding protein (LBP) and interleukin-6 (IL-6) using ELISA. In experiment 2, sixteen crossbred steers (576 ± 14.2 kg) fed the same diet were allotted by BW to the 0 and 200 mg/kg BW aspirin treatments (8 steers/treatment) and were slaughtered 24 h after the last dose. Jejunal tissues were collected and tight junction mRNA expression was determined. Data were analyzed using the MIXED procedure of SAS. Aspirin linearly increased Cr absorption (P = 0.02) and elimination (P = 0.04) rate and linearly decreased mean retention time of Cr (P = 0.02). Aspirin tended to increase jejunal claudin-1 mRNA expression (P = 0.10) but did not affect serum IL-6 or LBP or expression of other jejunal tight junction mRNA (P ≥ 0.20). This study indicates that aspirin disrupts GIT barrier function in beef cattle and has potential as a model in GIT permeability research.
The negative impacts of stress on gastrointestinal (GIT) barrier function can result in compromised animal health. Aspirin (acetylsalicylic acid) is known to cause mucosal injury leading to increased gut permeability and tight junction damage. The objective of this study was to determine the long-term impact of leaky gut on animal physiology. In this experiment, 96 Simmental x Angus steers (355 ± 14.8 kg) were allotted by body weight and breed into two treatments: control (no aspirin) or aspirin fed at 50 mg/kg/d for 159 d. Steers were housed in 16 pens (8 pens/treatment) with 6 steers in each pen. Weight was recorded monthly and serum was collected on d 159 to be analyzed for lipopolysaccharide binding protein (LBP), interleukin-6 (IL-6), serum amyloid A (SAA), haptoglobin, and aspartate aminotransferase (AST). Data were analyzed using the MIXED procedure of SAS. Average daily gain (ADG) tended to decrease in cattle fed aspirin (P= 0.10). Aspirin decreased hot carcass weight (P= 0.05) and rib-eye area (P= 0.01)and increased fat thickness (P= 0.02), marbling score (P = 0.003), and yield grade (P = 0.01). Percent KPH tended to increase (P= 0.10) for steers fed aspirin. Aspirin had no effect on body weight, dry matter intake, gain:feed, days on feed, dressing percentage, liver abscess score, or percent liver abscesses. Aspirin tended to increase serum LBP (P= 0.07), but had no effect on serum concentrations of IL-6, haptoglobin, SAA, and AST (P≥ 0.30). This study indicates that leaky gut induced by long-term administration of aspirin has negative impacts on feedlot performance and carcass leanness. The negative impact of aspirin induced leaky gut on animal performance suggests that leaky gut caused by other factors (subacute acidosis, stress) may be a significant problem for the feedlot industry.
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