Characterization of the cortisol response following an acute challenge with lipopolysaccharide in yellow perch and the influence of rearing density

Two experiments were performed to characterize the corticosteroid response of yellow perch Perca flavescens following an intraperitoneal injection of lipopolysaccharide (LPS) and determine if sustained differences in rearing density alter this response. In the first experiment, yellow perch were injected with LPS (3 mg kg � 1 ), saline, or handled without receiving any injection. Concentrations of cortisol in plasma were elevated in all groups relative to nondisturbed fish at 1� 5 and 3 h after handling but by 6 h after injection the mean concentration of cortisol in plasma from LPS-injected yellow perch were three to five times higher than fish before injection and significantly larger than groups of fish not treated with LPS. In the second test, yellow perch were held at different rearing densities (9 v. 18–19 kg m � 3 ) for 3, 7 and 14 days before injection with LPS (3 mg kg � 1 ). The cortisol response of yellow perch following LPS injection of fish held for 14 days at high density was significantly lower than that of fish held at the low density for the same duration. Additionally a trend of a decreased cortisol response to LPS injection as duration of holding increased was observed among fish held at high density relative to fish held at low density. These data illustrate that the corticosteroid response of yellow perch following LPS injection is distinct from handling alone and that the magnitude of the response is impacted by rearing density.

[1]  B. Barton Stress in Fishes: A Diversity of Responses with Particular Reference to Changes in Circulating Corticosteroids1 , 2002, Integrative and comparative biology.

[2]  C. Secombes,et al.  Cytokines and innate immunity of fish. , 2001, Developmental and comparative immunology.

[3]  S. MohanKumar,et al.  Effects of bacterial lipopolysaccharide on central monoamines and fever in the rat: involvement of the vagus , 2000, Neuroscience Letters.

[4]  J. Malison,et al.  Effects of Lighting Spectrum and Disturbance Level on the Growth and Stress Responses of Yellow Perch Perca flavescens , 2000 .

[5]  M. Kimura,et al.  The Mechanism of Action of Cytokines to Control the Release of Hypothalamic and Pituitary Hormones in Infection , 2000, Annals of the New York Academy of Sciences.

[6]  W. Langhans,et al.  Vagal and splanchnic afferents are not necessary for the anorexia produced by peripheral IL-1β, LPS, and MDP. , 1998, American journal of physiology. Regulatory, integrative and comparative physiology.

[7]  I. Bérczi Neurohormonal Host Defense in Endotoxin Shock , 1998, Annals of the New York Academy of Sciences.

[8]  B. McEwen Protective and damaging effects of stress mediators. , 1998, The New England journal of medicine.

[9]  J. Licinio,et al.  Pathways and mechanisms for cytokine signaling of the central nervous system. , 1997, The Journal of clinical investigation.

[10]  G. Nilsson,et al.  Serotonin as a regulator of hypothalamic-pituitary-interrenal activity in teleost fish , 1997, Neuroscience Letters.

[11]  Florian Holsboer,et al.  Long-Term Intracerebroventricular Infusion of Corticotropin-Releasing Hormone Alters Neuroendocrine, Neurochemical, Autonomic, Behavioral, and Cytokine Responses to a Systemic Inflammatory Challenge , 1997, The Journal of Neuroscience.

[12]  B. Barton,et al.  Physiological Responses of Juvenile Walleyes to Handling Stress with Recovery in Saline Water , 1995 .

[13]  A. Dunn The role of interleukin-1 and tumor necrosis factor α in the neurochemical and neuroendocrine responses to endotoxin , 1992, Brain Research Bulletin.

[14]  C. Schreck,et al.  Evidence for ultra-short-loop feedback in ACTH-induced interrenal steroidogenesis in coho salmon: acute self-suppression of cortisol secretion in vitro. , 1992, General and comparative endocrinology.

[15]  C. Audet,et al.  Impaired cortisol stress response in fish from environments polluted by PAHs, PCBs, and mercury , 1992, Archives of environmental contamination and toxicology.

[16]  R. D. Ewing,et al.  Cortisol and its effects on plasma thyroid hormone and electrolyte concentrations in fresh water and during seawater acclimation in yearling coho salmon, Oncorhynchus kisutch. , 1984, General and comparative endocrinology.

[17]  A. D. Pickering,et al.  Acclimation of the interrenal tissue of the brown trout, Salmo trutta L., to chronic crowding stress , 1984 .

[18]  L. Mawdesley-Thomas THE FISHERIES SOCIETY OF THE BRITISH ISLES , 1970 .

[19]  G. Wedemeyer Pituitary Activation by Bacterial Endotoxins in the Rainbow Trout (Salmo gairdneri) , 1969, Journal of bacteriology.

[20]  S. W. Wendelaar Bonga,et al.  Bacterial lipopolysaccharide (LPS) and interleukin 1 (IL-1) exert multiple physiological effects in the tilapia Oreochromis mossambicus (Teleostei) , 2004, Journal of Comparative Physiology B.

[21]  A. Hontela,et al.  Inhibition of cortisol secretion in dispersed head kidney cells of rainbow trout (Oncorhynchus mykiss) by endosulfan, an organochlorine pesticide. , 2001, General and comparative endocrinology.

[22]  C. Schreck Accumulation and long-term effects of stress in fish. , 2000 .

[23]  M. Manning,et al.  4 - The Specific Immune System: Cellular Defenses , 1996 .

[24]  F. Holsboer,et al.  The role of the hypothalamic-pituitary-adrenocortical system during inflammatory conditions. , 1994, Critical reviews in neurobiology.