Ovarian steroids modulate the systemic inflammatory response OF COWS challenged with lipopolysaccharide (LPS) intrauterine infusion

Postpartum uterine infections of dairy cows promote a local and systemic inflammation and interfere with reproductive efficiency. The aim of this study was to evaluate the effect of steroid hormones including progesterone (P4) and estradiol (E2) on the systemic inflammatory response of cows after be...

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Veröffentlicht in:Theriogenology 2022-04, Vol.182, p.35-44
Hauptverfasser: Magalhães, L.Q., Barbosa, S.P.F., Fagundes, N.S., Almeida, M.O., Carneiro, L.C., Brandão, F.Z., Nogueira, G.M., Pereira, E.C.M., Saut, J.P.E.
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Sprache:eng
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Zusammenfassung:Postpartum uterine infections of dairy cows promote a local and systemic inflammation and interfere with reproductive efficiency. The aim of this study was to evaluate the effect of steroid hormones including progesterone (P4) and estradiol (E2) on the systemic inflammatory response of cows after being challenged with an intrauterine infusion of lipopolysaccharide (LPS). For this, a hemogram and serum dosage of haptoglobin (Hp) in eight primiparous Gir cows ovariectomized were performed on day (day 0) and after 24 h (day +1). Four cows (n = 4) were challenged (day 0) with 20 mL of 0.9% NaCl + 12.5 μg/kg LPS, and four cows (n = 4) were challenged (day 0) with 20 mL of 0.9% NaCl. For this, the study was divided in four experimental groups as: (1) Control group: without any hormonal treatment before day 0; (2) Group 24 h - E2: 1 mg of estradiol benzoate 24 h before (day −1); (3) Group 24 h - P4: 2.0 g of P4 device 24 h before (day −1); (4) Group 14 d - P4: 2.0 g of P4 device 14 days before (day −14). In the systemic response to LPS, there was an increase in Hp (control group; 24 h - P4 group; 14 d - P4 group), and on day +1 the Hp of 14 d - P4 group was higher when compared to the other groups. On day 0, the 14 d - P4 group had an increase in circulating leukocytes and lymphocytes cells than the control group (P 
ISSN:0093-691X
1879-3231
DOI:10.1016/j.theriogenology.2022.01.027