Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Jul 23;15(15):2167.
doi: 10.3390/ani15152167.

Effects of Modified Attapulgite on Daily Weight Gain, Serum Indexes and Serum Metabolites in Fattening Beef Cattle

Affiliations

Effects of Modified Attapulgite on Daily Weight Gain, Serum Indexes and Serum Metabolites in Fattening Beef Cattle

Jiajie Wang et al. Animals (Basel). .

Abstract

In this study, we investigated the effects of dietary supplementation with thermally modified attapulgite on the daily weight gain, serum biochemical indices, and serum metabolites of Simmental fattening cattle. A total of 30 healthy Simmental fattening beef calves of similar age (8 to 9 months old) and body weight (370 ± 10 kg) were randomly divided into two groups, each containing 15 animals. A control group was fed the basal diet, and a treatment group was fed the same basal diet with the addition of 4 g/kg of thermally modified attapulgite. After 75 days of formal experiment, the calves in the two groups were weighed, and blood samples were collected by tail vein blood sampling for determinations of the serum biochemical indices and serum metabolites using liquid chromatography-mass spectrometry (LC-MS) analysis. The results indicated that the addition of thermally modified attapulgite to the diet had no significant effects on the daily weight gain of fattening beef cattle. After feeding with modified attapulgite, the glutathione peroxidase and superoxide dismutase activities in the serum of the experimental group were 55.02% (257.26 U·mL-1 to 165.95 U·mL-1, p < 0.05) and 13.11% (18.98 U·mL-1 to 16.78 U·mL-1, p < 0.05) higher than that in the control group. Compared with the control group, the tumor necrosis factor-alpha content was reduced by 14.50% (31.27 pg·mL-1 to 36.57 pg·mL-1, p < 0.01), and the concentration of interleukin-6 and lipopolysaccharide decreased by 17.00% (34.33 pg·mL-1 to 41.36 pg·mL-1, p < 0.001) and 23.05% (51.34 EU·L-1 to 66.72 EU·L-1, p < 0.001) in the serum of the experimental group. Contrastingly, the thermally modified attapulgite had no significant effects on the levels of serum total protein, albumin, or globulin in Simmental fattening cattle (p > 0.05). Furthermore, the results of serum metabolomic analyses revealed that there were a total of 98 differential metabolites, which were mainly enriched with respect to glycerophospholipid metabolism, Th1 and Th2 cell differentiation, autophagy-other, retrograde endogenous cannabinoid signaling, and the NF-κB signaling pathway. Overall, thermally modified attapulgite was found to effectively increase the activity of antioxidant enzymes, reduce serum inflammatory mediators, may suppress oxidative damage, enhance immunity, and have a positive influence on the health of Simmental fattening beef calves.

Keywords: antioxidant indicator; fattening beef cattle; inflammatory factor; modified attapulgite; serum metabolism.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Serum PLS-DA score (a) and PLS-DA model validation (b) plots. Note: N: experimental group serum samples, B: control group serum samples, QC: quality control samples, R2: model interpretability, Q2: model predictability. The closer the R2 and Q2 values are to 1, the more stable and reliable is the model.
Figure 2
Figure 2
Volcano plots of serum differential metabolites in anion (a) and cation (b) modes. Note: N: serum samples from the experimental group, B: serum samples from the control group.
Figure 3
Figure 3
Hierarchical clustering heat map of differential metabolites. Note: N: experimental group serum samples, B: control group serum samples. The red and blue colors indicate up- and downregulated expression of the differential metabolites, respectively.
Figure 4
Figure 4
A plot showing differential abundance scores. Note: The size of the dots indicates the number of differentially annotated metabolites in a pathway. The longer the line segment with the dots to the right of the central axis, the more upregulated is the overall expression of the pathway, whereas the longer the line segment with the dots to the left of the central axis, the more downregulated is the overall expression of the pathway. *** p-value < 0.001, ** p-value < 0.01, * p-value or < 0.05.

Similar articles

References

    1. Mendes S.J.F., Sousa F.I.A.B., Pereira D.M.S., Ferro T.A.F., Pereira I.C.P., Silva B.L.R., Pinheiro A.J.M.C.R., Mouchrek A.Q.S., Monteiro-Neto V., Costa S.K.P., et al. Cinnamaldehyde modulates LPS-induced systemic inflammatory response syndrome through TRPA1-dependent and independent mechanisms. Int. Immunopharmacol. 2016;34:60–70. doi: 10.1016/j.intimp.2016.02.012. - DOI - PubMed
    1. Triantafilou M., Triantafilou K. Lipopolysaccharide recognition: CD14, TLRs and the LPS-activation cluster. Trends Immunol. 2002;23:301–304. doi: 10.1016/S1471-4906(02)02233-0. - DOI - PubMed
    1. Wu Y., Sun Y., Dong X., Chen J., Wang Z., Chen J., Dong G. The Synergism of PGN, LTA and LPS in Inducing Transcriptome Changes, Inflammatory Responses and a Decrease in Lactation as Well as the Associated Epigenetic Mechanisms in Bovine Mammary Epithelial Cells. Toxins. 2020;12:387. doi: 10.3390/toxins12060387. - DOI - PMC - PubMed
    1. Wei X.F. Role and mechanism of AKT1 gene methylation in the decreased lactation ability of dairy cows induced by LPS. Northeast Agric. Univ. 2023 doi: 10.27010/d.cnki.gdbnu.2023.000360. - DOI
    1. Jiao B., Zhang W., Zhang C., Zhang K., Cao X., Yu S., Zhang X. Protein tyrosine phosphatase 1B contributes to neuropathic pain by aggravating NF-κB and glial cells activation-mediated neuroinflammation via promoting endoplasmic reticulum stress. CNS Neurosci. Ther. 2024;30:e14609. doi: 10.1111/cns.14609. - DOI - PMC - PubMed

LinkOut - more resources