Effects of continuously infusing glucose or casein into the terminal ileum on biomarkers of metabolism, inflammation, and intestinal morphology in growing pigs

Author(s):  
Edith J Mayorga ◽  
Erin A Horst ◽  
Mohmmad Al-Qaisi ◽  
Brady M Goetz ◽  
Megan A Abeyta ◽  
...  

Abstract Study objectives were to determine the effects of continuously infusing glucose (GLC) or casein (CAS) into the terminal ileum on biomarkers of metabolism, inflammation, and intestinal morphology in growing pigs. Crossbred gilts (n=19; 81±3 kg body weight [BW]) previously fitted with T-cannulas at terminal ileum were used in the current experiment. Following 4 d of acclimation, pigs were enrolled in 2 experimental 4-d periods (P). During P1, pigs were housed in individual pens and fed ad libitum for collection of baseline parameters. At the beginning of P2, pigs were assigned to 1 of 3 infusion treatments: 1) control (CON; water; 3 L/d; n=7), 2) GLC (dextrose 50%; 500 g/d; n=6;), or 3) CAS (casein sodium salt; 300 g/d; n=6). Water, GLC, and CAS solutions were continuously infused at a rate of 125 mL/h for the entirety of P2. Animals were euthanized at the end of P2, and intestinal tissue was collected. During P2, average daily feed intake differed across treatments and was reduced in GLC compared to CON pigs (14%), while CAS pigs consumed an intermediate amount (P=0.05). Average daily gain and final BW were similar across treatments. A treatment by time interaction was observed for blood urea nitrogen (BUN; P<0.01), as it decreased in GLC (21%) while it gradually increased in CAS (76%) pigs relative to CON pigs. Mild hyperthermia occurred with both GLC and CAS infusions relative to CON (+0.3 and 0.2°C, respectively; P<0.01). Blood neutrophils increased in CAS relative to CON pigs (26%) but remained similar between CON and GLC treatments (P<0.01). Blood monocytes decreased in GLC relative to CON pigs (24%) while CAS pigs had an intermediate value (P=0.03). Circulating lipopolysaccharide binding protein tended to decrease in GLC (29%) relative to CON pigs but remained similar between CON and CAS pigs (P=0.10). Plasma tumor necrosis factor-alpha was similar across treatments. Ileum villus height:crypt depth was increased in CAS compared to CON pigs (33%; P=0.05) while GLC pigs had an intermediate value. Colon myeloperoxidase-stained area increased in CAS compared to CON pigs (45%; P=0.03) but remained similar between GLC and CON pigs. In summary, continuously infusing GLC or CAS into the terminal ileum appeared to stimulate a mild immune response and differently altered BUN patterns but had little or no effects on blood inflammatory markers, intestinal morphology, or key production parameters.

2019 ◽  
Vol 97 (Supplement_2) ◽  
pp. 111-111
Author(s):  
Edith J Mayorga ◽  
Erin A Horst ◽  
Mohmmad Al-Qaisi ◽  
Carrie S McCarthy ◽  
Brady M Goetz ◽  
...  

Abstract Objectives were to determine the effects of continuously infusing glucose (GLU) or casein (CAS) at the terminal ileum on circulating metabolism and intestinal architecture in pigs. Crossbred gilts (81 ± 1 kg BW) fitted with ileocecal cannulas and jugular catheters were enrolled in 2 experimental periods (P). Period 1 (4 d) served for the collection of baseline measurements. At the beginning of P2 (4 d), pigs were assigned to 1 of 3 infusion treatments: 1) control (CTL; water; n = 7), 2) GLU (500 g/d; n = 6), and 3) CAS (300 g/d; n = 6). Water, GLU, and CAS solutions were continuously infused (125 mL/h) through the ileocecal cannula for the entirety of P2. Pigs were sacrificed following P2 and segments of jejunum, ileum, and colon were collected. Data were analyzed using the MIXED procedure of SAS. During P2, circulating glucose and non-esterified fatty acids were similar among treatments (P > 0.10). A tendency for a treatment × time interaction was observed for insulin as it decreased over time in CTL pigs, while it remained almost unchanged in GLU and CAS treatments during P2 (P = 0.07). Blood urea nitrogen (BUN) decreased in GLU relative to CTL pigs during P2 (21%; P = 0.01), whereas it gradually increased (76%; P < 0.01) from 6 to 96 h post-infusion in CAS pigs when compared to their CTL counterparts. No differences on fecal pH were observed across treatments (P = 0.62). Ileum villus height tended to increase in CAS relative to CTL pigs (P = 0.08). Similarly, ileum villus height:crypt depth was increased in CAS compared to CTL pigs (P = 0.02). Goblet cell area was similar across treatments but tended to decrease in the jejunum in GLU when compared to their CTL counterparts (P = 0.09). In conclusion, continuously infusing GLU or CAS into the terminal ileum differently altered BUN patterns, but surprisingly had little effects on intestinal morphology.


PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e9851
Author(s):  
Jian Ma ◽  
Ali Mujtaba Shah ◽  
Zhisheng Wang ◽  
Rui Hu ◽  
Huawei Zou ◽  
...  

Background Yak (Bos grunniens) is an ancient bovine species on the Qinghai-Tibetan Plateau. Due to extremely harsh condition in the plateau, the growth retardation of yaks commonly exist, which can reduce the incomes of herdsman. The gastrointestinal barrier function plays a vital role in the absorption of nutrients and healthy growth. Functional deficiencies of the gastrointestinal barrier may be one of the contributors for yaks with growth retardation. Methods To this end, we compared the growth performance and gastrointestinal barrier function of growth-retarded (GRY) and normal yaks (GNY) based on average daily gain (ADG), serum parameters, tissue slice, real-time PCR, and western blotting, with eight yaks in each group. Results GRY exhibited lower (P < 0.05) average daily gain as compared to GNY. The diamine oxidase, D-lactic acid, and lipopolysaccharide concentrations in the serum of GRY were significantly higher (P < 0.05) than those of GNY. Compared to GNY, the papillae height in the rumen of GRY exhibited lower (P = 0.004). In jejunum, with the exception of higher villus height, width, and surface area in GNY, numerical difference (P = 0.61) was detected between two groups for crypt depth. Both in rumen and jejunum, the mRNA expression of interleukin-1beta in GRY was markedly higher (P < 0.05) than that in GNY, but an opposite trend was found in interleukin-10 expression. Moreover, GRY showed a higher (P < 0.05) tumor necrosis factor-alpha mRNA expression in the rumen. The claudin-1 (CLDN1), occludin (OCLN), and zonula occludens-1 (ZO1) expressions of GRY in rumen and jejunum were significantly down-regulated (P < 0.05) as compared to GNY. The correlation analysis identified that in rumen and jejunum, there was a positive correlation between interleukin-10 and CLDN1, OCLN, and ZO1 mRNA expressions, but the tumor necrosis factor-alpha was negatively correlated with CLDN1, OCLN, and ZO1. In the rumen, the ADG was positively correlated with papillae surface area, and a same relationship between ADG and CLDN1, OCLN, and ZO1 expressions was found. Conclusion The results indicated that the ruminal and jejunal barrier functions of GRY are disrupted as compared to GNY. In addition, our study provides a potential solution for promoting the growth of GRY by enhancing the gastrointestinal barrier function.


1989 ◽  
Vol 90 (1) ◽  
pp. 11-15 ◽  
Author(s):  
Akram A. Mushtaha ◽  
Frank C. Schmalstieg ◽  
Thomas K. Hughes, Jr. ◽  
Elizabeth Rudloff ◽  
Armond S. Goldman

1989 ◽  
Vol 139 (4) ◽  
pp. 1010-1016 ◽  
Author(s):  
Elizabeth A. Rich ◽  
James R. Panuska ◽  
Robert S. Wallis ◽  
Christopher B. Wolf ◽  
Michelle L. Leonard ◽  
...  

2009 ◽  
Vol 88 (12) ◽  
pp. 743-752 ◽  
Author(s):  
BartŁomiej Baran ◽  
Iga Bechyne ◽  
Maciej Siedlar ◽  
Katarzyna Szpak ◽  
Bożenna Mytar ◽  
...  

1989 ◽  
Vol 257 (2) ◽  
pp. R451-R455 ◽  
Author(s):  
J. G. Cannon ◽  
R. A. Fielding ◽  
M. A. Fiatarone ◽  
S. F. Orencole ◽  
C. A. Dinarello ◽  
...  

Interleukin 1 beta (IL-1 beta) is a protein released from blood monocytes and related cells in response to infectious or inflammatory stimuli. Although IL-1 beta is elevated in the circulation for only a few hours after an acute inflammatory challenge or exercise, it has been proposed to mediate anabolic and catabolic processes that can last for several days. In this report, eccentric exercise was used as a noninfectious inflammatory stimulus. IL-1 beta was found in muscle tissue up to 5 days after exercise using specific immunohistochemical tissue staining. Increased IL-1 beta immunoreactivity was observed in muscle tissue from four human subjects who performed the exercise, but not in tissue obtained at the same time intervals from two subjects who did not exercise. Little immunohistochemical evidence of interleukin-1 alpha or tumor necrosis factor alpha was observed before or after exercise. These results implicate IL-1 beta in the metabolic adaptations of muscle tissue, which occur in response to noninfectious stresses.


2011 ◽  
Vol 11 ◽  
pp. 1886-1892
Author(s):  
Carlos R. Cámara-Lemarroy ◽  
Francisco J. Guzmán-de la Garza ◽  
Paula Cordero-Pérez ◽  
Gabriela Alarcón-Galván ◽  
Liliana Torres-Gonzalez ◽  
...  

Ischemia/reperfusion (I/R) is a condition that stimulates an intense inflammatory response. No ideal treatment exists. Triflusal is an antiplatelet salicylate derivative with anti-inflammatory effects. S-adenosylmethionine is a metabolic precursor for glutathione, an endogenous antioxidant. Dextromethorphan is a low-affinity N-methyl-D-aspartate receptor inhibitor. There is evidence that these agents modulate some of the pathways involved in I/R physiopathology. Intestinal I/R was induced in rats by clamping the superior mesenteric artery for 60 minutes, followed by 60 minutes of reperfusion. Rats either received saline or the drugs studied. At the end of the procedure, serum concentrations of tumor necrosis factor-alpha (TNF-alpha), malonaldehyde (MDA), and total antioxidant capacity (TAC) were determined and intestinal morphology analyzed. I/R resulted in tissue damage, serum TNF-alpha and MDA elevations, and depletion of TAC. All drugs showed tissue protection. Only triflusal reduced TNF-alpha levels. All drugs lowered MDA levels, but only triflusal and S-adenosylmethionine maintained the serum TAC.


1988 ◽  
Vol 254 (3) ◽  
pp. G450-G456 ◽  
Author(s):  
L. L. Moldawer ◽  
C. Andersson ◽  
J. Gelin ◽  
K. G. Lundholm

During inflammation, activated monocytes and lymphocytes synthesize and release many soluble protein mediators, such as interleukin (IL) 1, tumor necrosis factor-alpha, and IL-2. It is presently unclear which cytokines, if any, contribute to the anorexia and hepatic protein changes frequently seen during inflammation. To evaluate their potential role, food intake and liver and plasma protein synthesis were determined in both endotoxin-sensitive C57Bl/6j mice and endotoxin-resistant C3H/HeJ mice given either crude secretory products of Staphylococcus albus-stimulated human blood monocytes or murine recombinant IL-1-alpha, human recombinant IL-1-alpha or -beta, human recombinant tumor necrosis factor-alpha, or human IL-2. When given intraperitoneally to healthy animals, 2,000 lymphocyte-activating factor U/day of secretory products of activated human blood monocytes or recombinant murine IL-1-alpha depressed spontaneous food intake by 42 and 53%, respectively. Human IL-1-alpha and -beta and human tumor necrosis factor-alpha produced smaller reductions in food intake. In contrast, human IL-2, when given in equimolar quantities, had no appreciable effect on food intake or body weight. Administration of crude secretory products of activated blood monocytes, recombinant IL-1, or tumor necrosis factor-alpha increased liver weight, protein, and RNA content. In addition, plasma protein synthesis was significantly increased, as were serum amyloid P concentrations. Administration of recombinant tumor necrosis factor-alpha resulted in IL-1 production by peritoneal adherent cells. However, IL-2 had no effect on any hepatic parameter.


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