Downregulation of glucocorticoid receptors of liver cytosols and the role of the inflammatory cytokines in pathological stress in scalded rats.
Liu. Du-hu DH; Su. Yong-ping YP; Zhang. Wei W; Lou. Shu-fen SF; Ran. Xin-ze XZ; Gao. Jing-sheng JS; Cheng. Tian-min TM
Key Findings
- Severe scald injury sharply reduces glucocorticoid‑receptor binding in rat liver cytosol
- KPV peptide administration prevents the loss of receptor binding after injury
- KPV also attenuates the injury‑induced rise in IL‑1β, TNFα, IL‑10 and corticosterone
Practical Outcomes
- KPV shows anti‑inflammatory and glucocorticoid‑preserving effects in a rat burn model, suggesting it could help counter stress‑induced hormone resistance. However, the data are pre‑clinical, so no dosage or protocol can be recommended for humans yet.
Summary
In burned rats, a severe skin injury lowered liver glucocorticoid‑receptor levels and spiked stress hormones and inflammation. Giving the short peptide KPV (Ac‑D‑Lys‑L‑Pro‑D‑Val) stopped the receptor drop and reduced the hormone and cytokine spikes. The effect was similar to anti‑inflammatory antibodies and alpha‑MSH.
Abstract
Preliminary experiments indicated that target cells were resistant to glucocorticoid (GC) after pathological stress. This study was designed to investigate the alterations in plasma corticosterone level and GC receptor (GR) of liver cytosols, to assess the relative inflammatory cytokines contribution to GC resistant, and to observe the action of alpha-melanocyte-stimulating hormone (alpha-MSH) on the potential implications of glucocorticord regulatory effects in burned rats. Male Wistar rats (weight range, 180-200g) received a 35% total body surface area immersion scald and were randomly divided to receive either tumor necrosis factor alpha (TNFalpha), interleukin-1beta (IL-1beta), polyclonal antibody (pAb), alpha-MSH, Ac-D-Lys-L-Pro-D-Val (KPV peptide), or saline (control). The binding capacity (Rt) of the steroid-binding sites was measured by radioligand binding assay, using [3H]dexamethasone as the ligand. We examined plasma levels of IL-1beta, TNFalpha, IL-10, and corticosterone following scald challenge in rats. The Rt of GR (208.45+/-30.78fmol/mg of protein) in hepatic cytosol in rats, 12h later the scald was significantly lower than that (306.71+/-27.96fmol/mg of protein) of the control group (P<0.01). The injections of anti-rat TNFalpha (257.80+/-12.82fmol/mg of protein), IL-1beta antibody (254.46+/-21.21fmol/mg of protein), alpha-melanocyte-stimulating hormone (278.32+/-7.76fmol/mg of protein) and KPV peptide (263.46+/-17.46fmol/mg of protein) might prevent the Rt of GR from decreasing in hepatic cytosols of rats with scald, respectively (all of P<0.05) in vivo. Scald-induced robust increases in plasma IL-1beta (214.08+/-27.25pg/ml), TNFalpha (111.18+/-23.97pg/ml), IL-10 (177.50+/-15.79pg/ml) and corticosterone (2680+/-443.23ng/ml) levels after 12h. The administration of TNFalpha, IL-1beta pAb, alpha-MSH and KPV might attenuate these increases. These studies suggest that pro-inflammatory cytokines are involved in downregulation of GRs and thus alpha-MSH and KPV might increase the level of GR in rats with immersion scald.
Study Information
pubmed
2002
10.1016/s0305-4179(02)00011-6