ABSTRACT
Objective: Sleep apnea has been associated with anxiety, but the mechanisms of the sleep apnea-anxiety relationship are unresolved. Sleep apnea causes oxidative stress, which might enhance anxiety-like behavior in rodents. To clarify the apnea-anxiety connection, we tested the effect of intermittent hypoxia, a model of sleep apnea, on the anxiety behavior of mice. Methods: The rodents were exposed daily to 480 one-minute cycles of intermittent hypoxia to a nadir of 7±1% inspiratory oxygen fraction or to a sham procedure with room air. After 7 days, the mice from both groups were placed in an elevated plus maze and were video recorded for 10 min to allow analysis of latency, frequency, and duration in open and closed arms. Glyoxalase-1 (Glo1) and glutathione reductase-1 (GR1) were measured in the cerebral cortex, hippocampus, and striatum by Western blotting. Results: Compared to controls, the intermittent hypoxia group displayed less anxiety-like behavior, perceived by a statistically significant increase in the number of entries and total time spent in open arms. A higher expression of GR1 in the cortex was also observed. Conclusion: The lack of a clear anxiety response as an outcome of intermittent hypoxia exposure suggests the existence of additional layers in the anxiety mechanism in sleep apnea, possibly represented by sleepiness and irreversible neuronal damage.
Subject(s)
Animals , Male , Anxiety/etiology , Sleep Apnea Syndromes/complications , Glutathione Reductase/analysis , Lactoylglutathione Lyase/analysis , Hypoxia/complications , Anxiety/diagnosis , Anxiety/physiopathology , Sleep Apnea Syndromes/enzymology , Sleep Apnea Syndromes/physiopathology , Sleep Apnea Syndromes/psychology , Cerebral Cortex/enzymology , Oxidative Stress/physiology , Corpus Striatum/enzymology , Disease Models, Animal , Glutathione Reductase/metabolism , Lactoylglutathione Lyase/metabolism , Hypoxia/enzymology , Hypoxia/psychology , Mice, Inbred BALB CABSTRACT
Cashew nut shell oil has been reported to possess tumour promoting property. Therefore an attempt has been made to study the modulatory effect of cashew nut (Anlacardium occidentale) kernel oil on antioxidant potential in liver of Swiss albino mice and also to see whether it has tumour promoting ability like the shell oil. The animals were treated orally with two doses (50 and 100 microl/animal/day) of kernel oil of cashew nut for 10 days. The kernel oil was found to enhance the specific activities of SOD, catalase, GST, methylglyoxalase I and levels of GSH. These results suggested that cashew nut kernel oil had an ability to increase the antioxidant status of animals. The decreased level of lipid peroxidation supported this possibility. The tumour promoting property of the kernel oil was also examined and found that cashew nut kernel oil did not exhibit any solitary carcinogenic activity.
Subject(s)
9,10-Dimethyl-1,2-benzanthracene/toxicity , Anacardium/chemistry , Animals , Antioxidants/metabolism , Carcinogens/toxicity , Catalase/metabolism , Female , Glutathione/metabolism , Glutathione Transferase/metabolism , Lactoylglutathione Lyase/metabolism , Liver/drug effects , Mice , Microsomes, Liver/drug effects , Nuts/chemistry , Papilloma/chemically induced , Plant Oils/pharmacology , Skin Neoplasms/chemically induced , Superoxide Dismutase/metabolismABSTRACT
The activity of glyoxalase I from the soluble fraction of diabetic rat liver was found to decrease as compared to the control. Sodium orthovanadate in drinking water and Trigonella foenum graecum seed powder when administered to these diabetic animals were found to reverse the activity of glyoxalase I to control values. A combination of the above two antidiabetic compounds showed a better reversal. Vanadate and Trigonella seed powder treatment separately to diabetic rats also normalized hyperglycemia together with glyoxalase I activity. A combination of vanadate and Trigonella seed powder also restored the other general parameters of the diabetic animals.
Subject(s)
Animals , Diabetes Mellitus, Experimental/drug therapy , Female , Hypoglycemic Agents/pharmacology , Lactoylglutathione Lyase/metabolism , Liver/enzymology , Plant Extracts/pharmacology , Plants, Medicinal , Rats , Rats, Wistar , Trigonella , Vanadates/pharmacologyABSTRACT
Formaldehyde is a compound which is believed to have had a role in evolutionary processes. On the other hand, the (methyl)glyoxalase pathway is a route being present in all biological organisms whereas its function has not yet been recognized in the biochemical machinery. In this article it is raised that (methyl)glyoxalase path might have functioned as a bridge between formose and archaic reductive citric acid cycles in surface metabolists at the early stage of evolution. According to the theory, formaldehyde was essential for the mentioned system as a raw molecule. Based on thermodynamic calculations a simple way of regulation is also shown. The simplicity of the theory may be in a good agreement with and an explanation of why the (methyl)glyoxalase system is of ubiquitous nature.