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1.
Mol Cell Biochem ; 247(1-2): 83-94, 2003 May.
Article in English | MEDLINE | ID: mdl-12841635

ABSTRACT

Phagocytic cells contain NADPH oxidase that they use for host defense by catalyzing the production of superoxide. Bacterial lipopolysaccharide (LPS) has been found to stimulate NADPH oxidase in mobile and sessile macrophages and microglia. It also evokes fever in homeothermic animals and men, a reaction mediated by central nervous system (CNS) activities. The purpose of the present study was to determine whether reactive oxygen species are involved in LPS-induced fever. In rabbits we found that plasma hydroperoxide levels increased and catalase activity decreased 15 min after LPS injection and that fever started with a similar latency, while plasma levels of tumor necrosis factor-alpha (TNFalpha) increased 30 min after the injection. Treating rabbits with methylene blue or aspirin did not affect TNFalpha secretion but prevented the LPS-induced rise of hydroperoxides and the inactivation of catalase, abolishing fever. Incubation of human blood with nitroblue tetrazolium and LPS increased the number of formazan-positive neutrophils from 10 +/- 5 to 52 +/- 9%. Adding LPS to blood preincubated with either methylene blue, alpha-lipoic acid, or aspirin respectively decreased the number of formazan-positive neutrophils to 0.9 +/- 0.8, 0.8 +/- 0.9, or 2.0 +/- 0.9%, disclosing the antioxidant capacity of these drugs. Systemic application of 80 mg/kg alpha-lipoic acid elicited heat-loss reactions within 15 min and decreased core temperature by 2.2 +/- 0.3 degrees C within 2 h. Alpha-lipoic acid applied 45 min after LPS induced antipyresis within 15 min, and this antipyresis was associated with a decrease of elevated hydroperoxide levels and restoration of catalase activity. Our results show that fever is prevented when the production of reactive oxygen species is blocked and that an elevated body temperature returns to normal when oxygen radical production decreases. Estimation of plasma dihydrolipoic acid (DHLA) levels following injection of 80 mg/kg alpha-lipoic acid in afebrile and febrile rabbits revealed that this acid is converted into DHLA, which in afebrile rabbits increased the plasma DHLA concentration from 2.22 +/- 0.26 microg/ml to peak values of 8.60 +/- 2.28 microg/ml DHLA within 30 min and which in febrile rabbits increased it from 0.84 +/- 0.22 microg/ml to peak values of 3.90 +/- 0.94 microg/ml within 15 min. Methylene blue, aspirin, and alpha-lipoic acid, which all cross the blood-brain barrier, seem to act not only on peripheral tissues but also on the CNS. Brain structures that have been shown to sense oxidative stress are vicinal thiol groups attached to the NMDA subtype of glutamate receptor. Their reduction by thiol-reducing drugs like dithiothreitol or DHLA has been found to increase glutamate-mediated neuronal excitability, while the opposite effect has been observed after their oxidation. Because we found that systemic application of alpha-lipoic acid in the afebrile state elicits hypothermia and in the febrile state is antipyretic, we think this type of NMDA receptor is involved in thermoregulation and that oxidation of its thiol groups induces fever. It appears that temperature homeostasis can be maintained only if the redox homeostasis of the brain is guaranteed.


Subject(s)
Aspirin/pharmacology , Fever/prevention & control , Methylene Blue/pharmacology , Reactive Oxygen Species/metabolism , Thioctic Acid/analogs & derivatives , Thioctic Acid/pharmacology , Animals , Antioxidants/metabolism , Bacterial Infections/complications , Bacterial Infections/etiology , Brain/drug effects , Brain/metabolism , Catalase/blood , Catalase/cerebrospinal fluid , Endotoxins/blood , Endotoxins/cerebrospinal fluid , Female , Fever/etiology , Fever/metabolism , Formazans/analysis , Formazans/metabolism , Hydrogen Peroxide/blood , Hydrogen Peroxide/cerebrospinal fluid , Injections, Intravenous , Lipopolysaccharides/administration & dosage , Lipopolysaccharides/blood , Lipopolysaccharides/cerebrospinal fluid , Perfusion , Rabbits , Subarachnoid Space/drug effects , Subarachnoid Space/metabolism , Thioctic Acid/metabolism , Thioctic Acid/pharmacokinetics , Tumor Necrosis Factor-alpha/metabolism
2.
Ann N Y Acad Sci ; 966: 483-90, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12114308

ABSTRACT

Thirteen female patients suffering from fibromyalgia (FM) and thirteen female age-matched controls were intravenously injected with a bolus dose of 100 microg corticotropin-releasing hormone (CRH), and the evoked secretion pattern of ACTH, cortisol, somatostatin, and growth hormone (GH) was followed up for two hours, together with the plasma levels of CRH. The increases of ACTH and cortisol following CRH were not significantly different between controls and FM patients. The increase of plasma CRH following its injection was significantly higher in FM patients and lasted about 45 min, paralleled by an increase of somatostatin with a similar time course. Basal GH levels were significantly lower in FM patients. GH increased in FM patients 90 min after injection of CRH, coincident with decreasing CRH and somatostatin levels, while GH levels in controls rather decreased with the lowest values occurring 90 min after CRH. The results support the concept that the hormonal secretion pattern frequently observed in FM patients is primarily caused by CRH, possibly as a response to chronic pain and stress. The elevated levels of CRH in the circulation of FM patients suggest elevated levels of CRH-binding protein, which could explain why the levels of ACTH and cortisol between controls and FM following CRH do not differ.


Subject(s)
Adrenocorticotropic Hormone/metabolism , Corticotropin-Releasing Hormone , Fibromyalgia/physiopathology , Hydrocortisone/metabolism , Hypothalamo-Hypophyseal System/physiopathology , Pituitary-Adrenal System/physiopathology , Adrenal Cortex/drug effects , Adrenal Cortex/metabolism , Case-Control Studies , Female , Human Growth Hormone/metabolism , Humans , Middle Aged , Pituitary Gland, Anterior/drug effects , Pituitary Gland, Anterior/metabolism , Secretory Rate/drug effects , Sex Characteristics , Somatostatin/metabolism , Stress, Physiological/physiopathology
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