ABSTRACT
The neuroprotective effect of hypoxic preconditioning on kainate (KA)-induced neurotoxicity, including apoptosis and necrosis, was investigated in rat hippocampus. Female Wistar-Kyoto rats were subjected to 380 mm Hg in an altitude chamber for 15 h/day for 28 days. Intrahippocampal infusion of KA was performed in chloral hydrate anesthetized rats, which acutely elevated 2,3-dihydroxybenzoic acid levels in normoxic rats. Seven days after the infusion, KA increased lipid peroxidation in the infused hippocampus and resulted in hippocampal CA3 neuronal loss. A 4-week hypoxic preconditioning attenuated KA-induced elevation in hydroxyl radical formation and lipid peroxidation as well as KA-induced neuronal loss. The effects of hypoxic preconditioning on KA-induced apoptosis and necrosis were investigated further. Two hours after KA infusion, cytosolic cytochrome c content was increased in the infused hippocampus. Twenty-four hours after KA infusion, pyknotic nuclei, cellular shrinkage, and cytoplasmic disintegration, but not TUNEL-positive staining, were observed in the CA3 region of hippocampus. Forty-eight hours after KA infusion, both DNA smear and DNA fragmentation were demonstrated in the infused hippocampus. Furthermore, TUNEL-positive cells, indicative of apoptosis, in the infused hippocampus were detected 72 h after KA infusion. Hypoxic pretreatment significantly reduced necrotic-like events in the KA-infused hippocampus. Moreover, hypoxic preconditioning attenuated apoptosis induced by KA infusion, including elevation in cytosolic cytochrome c content, TUNEL-positive cells, and DNA fragmentation. Our data suggest that hypoxic preconditioning may exert its neuroprotection of KA-induced oxidative injuries via attenuating both apoptosis and necrosis in rat hippocampus.
Subject(s)
Excitatory Amino Acid Agonists/toxicity , Hippocampus/drug effects , Ischemic Preconditioning/methods , Kainic Acid/toxicity , Oxygen/metabolism , Animals , Blotting, Southern/methods , Blotting, Western/methods , Cell Count/methods , Chromatography, High Pressure Liquid/methods , Cytochromes c/metabolism , DNA Fragmentation/drug effects , Electrochemistry/methods , Female , Hippocampus/metabolism , Hippocampus/pathology , Hydroxybenzoates/analysis , In Situ Nick-End Labeling/methods , Lipid Peroxidation/drug effects , Microdialysis/methods , Neurons/pathology , Rats , Rats, Inbred WKY , Staining and Labeling/methods , Time FactorsABSTRACT
Two groups of mice were fed with either hedgehog hydnum powder or extract for sixty days. For the assay of fatigue, the activity of serum lactate dehydrogenase, the serum urea nitrogen content, blood lactic acid, hepatic and muscular glycogen, and the physical stamina of the mice were determined. The activity of serum lactate dehydrogenase and the hepatic and muscular glycogen content in the experimental mice were evidently higher than that in the control mice (P < 0.05 or P < 0.01). After exercise, the increase in blood lactic acid and serum urea nitrogen in the experimental mice was significantly lower than that in the control mice (P < 0.05 or P < 0.01), but the rate of elimination of blood lactic acid in the experimental mice was significantly higher than that in the control mice (P < 0.05). In the physical stamina swimming, the experimental mice drowned after a longer period of time than the control mice (P < 0.05). In conclusion hedgehog hydnum had a significant effect on raising physical stamina and delaying fatigue in mice.
Subject(s)
Basidiomycota , Fatigue/prevention & control , Animals , Blood Urea Nitrogen , L-Lactate Dehydrogenase/blood , Lactates/metabolism , Liver Glycogen/metabolism , MiceABSTRACT
We conducted a case-control study to examine the associations between various behavioral risk factors and urinary tract infection among college-aged women. Cases were collected from a University Health Service, and were compared to Health Service controls and to a population-based control group. Sexual intercourse, diaphragm use, and urinating after sexual intercourse were each associated with urinary tract infection (UTI). The magnitude of the association of diaphragm use with UTI was reduced when urination habits around sexual intercourse were considered.
PIP: 468 women using the University of Michigan Health Service because of urinary symptoms, completed questionnaires regarding medical history, stress, clothing, diet, sexual activity, and birth control method during the previous 4 weeks. 1484 potential Health Service controls without urinary symptoms were selected as well as 115 student-population -based controls. Urinary tract infection (UTI) criteria were 100,000 colonies of bacteria/ml urine and 10,000 colonies of a single bacteria/ml urine. After exclusions, the sample numbered 1641 women: 237 UTI cases, 1296 Health Service controls, and 108 student-population controls with an average age of 21.9 years. 63.2% of cases, 36.4% of Health Service controls, and 25.2% of population controls reported previous UTIs. UTIs significantly increased with the frequency of sexual intercourse. There was a weak link between a new sexual relationship in the prior 4 weeks and UTI and no association between multiple partners and UTI. Women without UTI used a diaphragm with spermicides (DIS) 8 times more often than oral contraceptives (OCs) compared to controls. Women who had had 1 or 2 UTIs used the DIS twice as often as OCs. Cases were more likely never of rarely to urinate after intercourse than controls. Always urinating before or after intercourse tended to protect against UTI. The odds ratio (OR) among women without UTI using a D/S urinating only before was 3.4, less than the OR of 9.5 associated with constant urination habits. The OR with D/S use before and after. Vitamin C appeared to protect against UTI, and the stress scale was somewhat linked to UTI. Sexual intercourse, D/S use, and urinating after sex (among women without previous UTI incidence) were associated with UTI.
