Objectives: The purpose of this study was to examine the relation between exercise intensity and immune function. Methods: Ten healthy young males underwent a constant work rate exercise of three levels, 90%, 80% and 70% ventilatory threshold (VT) work rate, for 20 min on a bicycle ergometer. These work rates were calculated for each individual based on his VT work rate obtained by the incremental exercise tests. Blood samples were collected before and after the exercise, and immune function indices were measured. Results: Compared with the obtained Vo2 at VT (VTVo2) in the incremental test, the Vo2 with the exercise of 70% VT work rate was at a similar level and the one with the exercise of 90% or 80% VT work rate had a significantly greater value. The numbers of leukocytes and neutrophils significantly increased in the 90% and 70% VT work rate groups. In 80% VT work rate group, the CD4/CD8 ratio was significantly depressed. The CD16+CD57− (%), natural killer cell populations, had a tendency to increase at 80% VT work rate, and also the CD16+CD57 + (%) had a similar tendency at 90% or 80% VT work rate. Conclusions: This study shows that moderate exercise reaching or exceeding the VT level acutely affects T cell and NK cell subsets.
Work ; Tachycardia, Ventricular ; Exercise ; Leukocytes ; immune function

Ischemia-reperfusion injury (IRI) is an inevitable consequence of organ transplantation that has major consequences for graft-and patient survival. During transplantation procedures, allografts are exposed to various periods of complete ischemia. Ischemic insult starts with brain death, and its associated hemodynamic disturbances continue during donor organ procurement, cold preservation, and implantation. Ischemia-reperfusion injury, which is a risk factor for acute graft injury, delayed graft function, and acute and chronic rejection, is triggered following reperfusion. Along the cascade of pathogenic events that accompany ischemic insults and cause IRI, there has been an appreciation for various immune mechanisms within the allograft itself. The pathophysiological events associated with IRI originate in signals derived from pattern recognition receptors (PRRs) expressed in the donor organ. Danger associated molecular patterns (DAMP) released from injured cells serve as ligands for PRRs expressed on many cells in the donor organ. Activation of PRR signaling in the donor organ leads to production of proinflammatory cytokines and activates the innate immune system, triggering adaptive immune responses as well as cell death signaling, ultimately worsening the initial ischemic injury. Accordingly, deciphering the inflammatory pathway of innate immunity in IRI may provide a good therapeutic target to block acute sterile inflammation caused by tissue damage.
Allografts ; Brain Death ; Cell Death ; Cytokines ; Delayed Graft Function ; Hemodynamics ; Humans ; Immune System ; Immunity, Innate ; Inflammation ; Ischemia* ; Ligands ; Organ Transplantation ; Porcine Reproductive and Respiratory Syndrome ; Receptors, Pattern Recognition ; Reperfusion ; Reperfusion Injury* ; Risk Factors ; Tissue and Organ Procurement ; Tissue Donors ; Transplantation ; Transplants

BACKGROUND: Chronic inflammation can lower the seizure threshold and have influence on epileptogenesis. The components of red ginseng (RG) have anti-inflammatory effects. The abundance of peripherally derived immune cells in resected epileptic tissue suggests that the immune system is a potential target for anti-epileptogenic therapies. The present study used continuous electroencephalography (EEG) to evaluate the therapeutic efficacy of RG in intrahippocampal kainic acid (IHKA) animal model of temporal lobe epilepsy.METHODS: Prolonged status epilepticus (SE) was induced in 7-week-old C57BL/6J mice via stereotaxic injection of kainic acid (KA, 150 nL; 1 mg/mL) into the right CA3/dorsal hippocampus. The animals were implanted electrodes and monitored for spontaneous seizures. Following the IHKA injections, one group received treatments of RG (250 mg/kg/day) for 4 weeks (RG group, n=7) while another group received valproic acid (VPA, 30 mg/kg/day) (VPA group, n=7). Laboratory findings and pathological results were assessed at D29 and continuous (24 h/week) EEG monitoring was used to evaluate high-voltage sharp waves on D7, D14, D21, and D28.RESULTS: At D29, there were no differences between the groups in liver function test but RG group had higher blood urea nitrogen levels. Immunohistochemistry analyses revealed that RG reduced the infiltration of immune cells into the brain and EEG analyses showed that it had anticonvulsant effects.CONCLUSION: Repeated treatments with RG after IHKA-induced SE decreased immune cell infiltration into the brain and resulted in a marked decrease in electrographic seizures. RG had anticonvulsant effects that were similar to those of VPA without serious side effects.
Animals ; Blood Urea Nitrogen ; Brain ; Electrodes, Implanted ; Electroencephalography ; Epilepsy, Temporal Lobe ; Hippocampus ; Immune System ; Immunohistochemistry ; Inflammation ; Kainic Acid ; Liver Function Tests ; Mice ; Models, Animal ; Panax ; Seizures ; Status Epilepticus ; Temporal Lobe ; Valproic Acid