Akihiro Ogata

Effects of body posture on local sweating and sudomotor outflow as estimated using sweat expulsion

To estimate the effects of changes in body posture on sudomotor function, sweat rates on the forearm, chest and thigh, tympanic temperature (Tty), and skin temperatures were recorded in an upright sitting and a supine position under a hot environment of 40 degrees C Ta and 40% relative humidity for 60 min. Sweat expulsions were identified on sweat rate curves and their rates (Fsw) were calculated. Tty was higher, and its initial fall was greater, in the supine position than in the sitting position. On the forearm and the chest, the regression line relating sweat rate to mean body temperature (Tmb) had a gentler slope in the supine position, whereas on the thigh, it showed a steeper slope. The regression line relating Fsw to Tmb had a steeper slope in the supine position than in the sitting position, suggesting that the gain in the mechanisms for central integration and rhythm-generation was enhanced in the supine position. The parameter of sweat rate divided by Fsw was lower on the forearm and the chest, whereas it was higher on the thigh in the supine position than in the sitting position, suggesting that sudomotor outflow was modified at the spinal cord in association with skin pressure. It was concluded that body posture affects sudomotor functions through both brain and spinal mechanisms.

Effect of body posture on central sudomotor mechanism estimated by the frequency of sweat expulsion

in the CG in comparison with the SCG. The percentage of SOM-positive cells in the SCG significantly decreased from birth onwards and we observed only single cells in 10-day-old and older animals. Meanwhile, the proportion of SOM-immunoreactive cells in the CG was not change during the development. SP was found in single neurons in the CG and SCG. NADPH-diaphorase positive cells were absent in the SCG and CG. In conclusion, the neurotransmitter composition in the SCG,CGand IG is present even in newborn animals. However, these ganglia develop heterochronously. Finally, the neurotransmitter set becomes complete by the second month of life. This work was supported by RFBR grants.