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The mechanism of human thermal comfort is important for building a comfortable and healthy indoor environment. This paper analyzes human heart rate variability (HRV) at different thermal comfort levels and discusses the mechanism of human thermal comfort. A total of 33 subjects were divided in 3 groups. Under air temperatures of 21, 24, 26, 28, 29, and 30 degrees C, the subjects' electrocardiogram was recorded for 5 min. HRV (the ratio of absolute powers in low- and high-frequency bands, LF/HF ratio) was analyzed. LF/HF at discomfort level were significantly higher than that at comfort level (P < 0.05), despite the same thermal sensation. The results indicate that sympathetic activity plays an important role in subjects' thermal discomfort and the LF/HF ratio may be used as an indicator for human thermal comfort.

Gender difference in thermal comfort for Chinese people was investigated through two laboratory experiments. Both subjective assessment and objective measurement were taken during the experiment. Skin temperature (17 points) and heart rate variability (HRV) were measured in one of the experiment. Our results show that there are gender differences in thermal comfort for Chinese people. Correlation of thermal sensation votes and air temperature and vapor pressure shows that females are more sensitive to temperature and less sensitive to humidity than males. Subjective assessment, skin temperature and HRV analysis suggest that females prefer neutral or slightly warmer condition, due to their constantly lower skin temperature and the fact that mean skin temperature is a good predictor of sensation and discomfort below neutrality. Female comfortable operative temperature (26.3 degrees C) is higher than male comfortable operative temperature (25.3 degrees C), although males and females have almost the same neutral temperature and that there is no gender difference in thermal sensation near neutral conditions.

1. The serotoninergic system is known to be involved in the control of multiple behavioural and physiological functions. The serotonin (5-hydroxtryptamine; 5-HT) transporter (SERT), which controls the synaptic 5-HT concentration through re-uptake of this neurotransmitter into presynaptic terminals, has been a primary therapeutic target for various psychiatric and peripheral disorders. The aim of the present study was to identify the regulatory mechanism(s) of the human SERT (hSERT) in heterologously expressed oocytes. 2. The hSERT cRNA was transcribed in vitro and injected into Xenopus oocytes. The 5-HT-induced transporter currents were measured by voltage clamp. The effects of extracellular sodium or chloride were studied by replacement perfusion with tetramethylammonium-chloride (96 mmol/L) or sodium acetate (96 mmol/L). In addition, to alter the internal calcium concentration, CaCl2 (50 micromol/L) and inositol triphosphate (IP3; 50 micromol/L), with or without EGTA (2.5 mmol/L), were injected into oocytes. The specificity of 5-HT-sensitive currents was determined by the use of the SERT antagonist desipramine and niflumic acid to block background chloride currents. 3. The hSERT-expressing oocytes displayed voltage-dependent, 5-HT-induced currents that increased at negative potentials. Replacing extracellular sodium or chloride significantly decreased the hSERT currents by 89 and 45%, respectively (P < 0.05, n = 7 each). Injection of IP3 or CaCl2 increased the hSERT currents by approximately 65% (P < 0.05; n = 10 each) and the effect of IP3 was abolished by preinjection of EGTA. 4. These results demonstrate that hSERT activity is not only voltage dependent, but is also affected by intracellular calcium and extracellular sodium and chloride.

Introduction: The slow component of the delayed rectifier K+ current IKs modulates repolarization of the cardiac action potential (AP), and the loss of IKs is known to cause long QT1 (LQT1) syndrome by prolonging action potential duration (APD). In this study, we generated a guinea pig LQT1 syndrome model using the IKs blocker chromanol 293B and then assayed the electrophysiologic effects of the ATP-sensitive potassium channel IK,ATP opener nicorandil on this model., Methods and Results: Transmembrane action potentials of perfused right ventricular papillary muscle preparations and both in vitro and in vivo ECGs of guinea pigs were recorded. Blockade of IKs by chromanol 293B (30 microM) prolonged the action potential duration at 90% repolarization (APD90) by 8.5% and QT interval by 16.5% of control values. In addition, proarrhythmic early afterdepolarizations (EADs) and ventricular fibrillation were observed. Venoinjection of chromanol 293B (1 mg/kg) revealed 10.9% QT prolongation. Nicorandil (5-30 microM) dose-dependently shortened APD90 under the control condition, whereas it reversed the AP prolongation effect of chromanol 293B by 7.4% at the 30 microM concentration. Moreover, nicorandil shortened QT intervals both in vitro and in vivo and displayed an inhibitory effect on EADs and ventricular fibrillation., Conclusion: The ATP-sensitive potassium channel opener nicorandil may be an effective drug in the therapy of LQT1 syndrome by shortening APD and the QT interval.