1. Red blood cell cholinesterase activity was decreased an average of
-31 +/- 9%, -41 +/- 8%, -35 +/- 7% and -41 +/- 13% after 2, 26, 50 and
74 h of pyridostigmine treatment (30 mg, t.i.d.). 2. Pyridostigmine d
ecreased resting heart rate at sea level (SL) by 7 +/- 10 b.min-1 afte
r 74 h (P < 0.05). Resting esophageal temperature (T(es)) was -0.28 +/
- 0.16-degrees-C at 10,000 ft and -0.10 +/- 0.22-degrees-C after 74 h
(SL) compared to SL control; and was +0.20 +/- 0.10-degrees-C after 2
h and +0.20 +/- 0.13-degrees-C after 26 h at 10,000 ft compared to alt
itude control (P < 0.05). 3. The thermosensitivity of forearm sweating
to increasing T(es) was 26 +/- 3% lower at altitude compared to sea l
evel (P < 0.05). This depression in thermosensitivity was not observed
at altitude with pyridostigmine. The T(es) threshold for onset of for
earm sweating was increased 0.2-degrees-C after 26 h of pyridostigmine
compared to control altitude experiments (P < 0.05). 4. The depressin
g effect of acute hypobaric hypoxia on thermosensitivity of sweating w
as confirmed by this study. Pyridostigmine administration did not affe
ct skin blood flow responses during acute altitude exposure.