| Literature DB >> 27350991 |
Abstract
The sex differences of infection and inflammatory diseases particularly appear at reproductive age and depend on the sex hormone level, varied between male and female. There are a few sets of data about the sex differences of infection and inflammatory diseases course, including systemic inflammatory response syndrome (SIRS) and sepsis, of newborns. The aim of our research was the estimation of morphological and immunological manifestation of SIRS of the newborn Wistar rats. Investigations were carried out on male and female two-day-old Wistar rats (10-12 g). SIRS was modeled by intraperitoneal injection of LPS (E. coli, O26: B6 strain, Sigma) in high dose-15 mg/kg. We did not find out any sex differences of the liver lesions severity between newborn males and females after LPS injection. The levels of endotoxin and estradiol in the serum, as the number of neutrophils in the intra-alveolar septa of the lungs, were higher in males than females with SIRS. Production of IL-2 and TNF-α by the spleen cells of males was higher than that in control group that reflects polarization predominantly on the Th1-type immune response. The secretion of IL-2, TNF-α, and IFN-γ by ConA activated spleen cells of females decreased that reflects the suppression of Th1-type immune response. We suppose that the LPS administration in the high dose causes the multidirectional reaction of the immune system of neonatal males and females Wistar rats.Entities:
Year: 2014 PMID: 27350991 PMCID: PMC4897487 DOI: 10.1155/2014/190749
Source DB: PubMed Journal: Int Sch Res Notices ISSN: 2356-7872
Endotoxin, corticosterone, and sex hormones levels in the serum of 2-day-old male and female Wistar rats in two control groups and on the 1st day after LPS injection (Med: 25%–75%).
| Females | Males | |||
|---|---|---|---|---|
| Control group | LPS 1 | Control group | LPS 1 | |
| Endotoxin (eU/ml) | 1.9 (0.5–3.3) | 57* (47.3–90.7) | 0.5 (0.1–2.6) | 33.5∗& (29.7–44.3) |
| Corticosterone (nmol/l) | 122.3 (112–440) | 436.3 (235.5–447.5) | 215.1 (35.9–340) | 351.3 (210.6–460) |
| Total testosterone (ng/ml) | 0.2 (0.2-0.3) | 0.4 (0.2–0.5) | 0.3 (0.1–3.3) | 1.7 (1.5–2.1) |
| Estradiol (pg/ml) | 32.9 (32–34.5) | 19.5 (13.2–21.8) | 22.2# (20.2–24.6) | 8.4* (6.7–21.5) |
| Progesterone (ng/ml) | 1.2 (0.6–1.2) | 0.5 (0.2–0.8) | 0.8 (0.7-0.8) | 0.5 (0.3–0.8) |
| ALT (eU/l) | 22 (13–41) | 107* (89–222) | 50.5 (29–74) | 102* (52–174) |
| AST (eU/l) | 264 (217–422) | 512 (244–685) | 197 (132.5–371.5) | 294 (179–343) |
Med: median, 25%–75%: interquartile range, LPS 1: the 1st day after LPS injection, *differences which are statistically significant as compared with the corresponding control group, &differences which are statistically significant between males and females after LPS injection, and #differences which are statistically significant between control groups of males and females.
Production level of cytokines by ConA activated splenic cells and neopterin and TGF-β concentration in the serum of 2-day-old males and females in two control groups and on the 1st day after LPS injection (Med: 25%–75%).
| Females | Males | |||
|---|---|---|---|---|
| Control group | LPS 1 | Control group | LPS 1 | |
| IL-2 (pg/ml) | 4403 (2378–6093) | 456.3* (386.1–617.8) | 141.7# (124.6–158.8) | 474.4* (426.1–826.2) |
| IL-4 (pg/ml) | 0.2 (0–0.9) | 0.4 (0.1–0.8) | 0.1 (0–0.3) | 0.3 (0–0.6) |
| IFN- | 48.9 (32.2–57.9) | 0* (0-0) | 0.9# (0.3–10.9) | 0* (0-0) |
| TNF- | 169.7 (123.6–255.8) | 89.8* (67.4–128.8) | 10.8# (1.3–13.5) | 51.2* (41.8–70.1) |
| Neopterin (нмольл) | 7 (5.7–10.8) | 14.2* (11.6–14.2) | 9.1 (7.1–10.4) | 7.3 (6–8.7) |
| TGF- | 18.6 (16.1–20.9) | 14.5 (15.2–18.2) | 18.9 (16.8–27.1) | 17 (15.2–18.2) |
Med: median, 25%–75%: interquartile range, LPS 1: the 1st day after LPS injection, *differences which are statistically significant as compared with the corresponding control group, and #differences which are statistically significant between control groups of males and females.
Figure 1Variability of pathologic changes of the liver of 2-day-old rats of both sexes on the 1st day after LPS injection. (a) Mild dystrophic changes of hepatocytes (male). (b) Severe dystrophic changes of hepatocytes (female). (c) Mild dystrophic changes of hepatocytes (female). (d) Vascular congestion, stasis, and sludge (male). (e) Landscape necrosis (female). (f) Necrosis and severe dystrophic changes of hepatocytes (male). Hematoxylin and eosin staining. ×640.
Figure 2The semiquantitative assessment of the liver lesions severity of newborn male (M) and female (F) Wistar rats on the 1st day after LPS injection.
Figure 3Morphologic changes in the lung of female ((a), (c)) and male ((b), (d)) 2-day-old rats on the 1st day after LPS injection. Vast areas of alveolar edema and gaps filled with alveolar erythrocytes and edematous liquid ((a), (b)). Diffusely scattered polymorphonuclear leukocytes in intra-alveolar septa around blood vessels ((c), (d)). Hematoxylin and eosin staining. (a), (b) ×320; (c), (d) ×640.
Figure 4Neutrophil number in intra-alveolar septa of the lung of newborn male (M) and female (F) Wistar rats in two control groups (F, M) and on the 1st day after LPS injection (F + LPS, M + LPS). Symbols: ∗ means that differences are statistically significant as compared with the corresponding control group; ∧ means that differences are statistically significant as compared with the LPS injected females.