By Chris Hughes

ISBN-10: 8090377831

ISBN-13: 9788090377837

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6, left), albeit contrast with results of Bachoo and Polosa [1]. Nevertheless, it is obvious from our studies that there is a close coupling between the RRG and SRGS in neonates. In conclusion, while the outputs of the neonatal RRG and SRGS resemble those of adult mammals, there are response patterns occurring in neonates that are not present in adult mammals. Furthermore, the absence of some responses in the developing mammal implies considerable postnatal maturation of the interactions between these two systems.

To the best of our knowledge, this has not been observed in adult mammals. A spontaneous change in output from the RRG (Fig. 5) was seen as an increase in PHR burst. Since the animal was on the cycle-triggered pump, the lung inflation was greater than normal. The effects on the output of the SRGS were quite interesting: initially an increase in the integrated signal, followed by a greater than normal decrease in activity that paralleled the augmented lung inflation. Thus, this figure demonstrates both central and peripheral RESP modulation of SYMP activity.

Am J PhysioI231:1601-1607 Barman SM, Gebber GL (1980) Sympathetic nerve rhythm of brain stem origin. Am J PhysioI239:R42-R47 Barman SM, Gebber GL (1981) Brain stem neuronal types with activity patterns related to sympathetic nerve discharge. Am J Physiol 240:R335-R347 Christakos CN, Cohen MI, See WR, Barnhardt R (1988) Fast rhythms in the discharges of medullary inspiratory neurons. Brain Res 463:362-367 Christakos CN, Cohen MI, See WR, Barnhardt R (1989) Changes in frequency content of inspiratory neuron and nerve activities in the course of inspiration.

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BAC TSR.2 The White Ghost #1004 Photo Hobby Manual by Chris Hughes


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