TY - JOUR
T1 - The effect of pyridostigmine on respiratory function in healthy and asthmatic volunteers
AU - Rami, Z.
AU - Molcho, M.
AU - Danon, Y. L.
AU - Almog, S.
AU - Baniel, J.
AU - Karni, A.
AU - Shemer, J.
PY - 1991
Y1 - 1991
N2 - Respiratory function was evaluated in 12 healthy and 13 asthmatic volunteers following a single oral dose of pyridostigmine in a double-blind, placebo-controlled cross-over study. Respiratory function tests were performed at rest and after submaximal exercise at the time corresponding to the expected peak cholinesterase inhibition by pyridostigmine. A single dose of 60 mg pyridostigmine given to nonasthmatic subjects led to a decrease of 28.4% in cholinesterase activity when compared to the baseline and a statistically (but not physiologically) significant decrease in FEV1 (forced expiratory volume in 1 sec) both at rest (P<0.015) and after exercise (P<0.05). This effect showed a strong correlation to the degree of cholinesterase inhibition (r = -0.936, P<0.0001). According to these findings, a smaller dose of pyridostigmine (30 mg) was given to subjects with mild bronchial asthma. At that dose, pyridostigmine resulted in a similar inhibition of cholinesterase activity to a mean of 76.7% of the baseline. A significant decrease in the pulse rate was also found (P<0.005). However, no changes in respiratory function were observed when compared with the effects of placebo. The effect of post-exertion atropine inhalation on respiratory function was also unchanged with pyridostigmine at that dose. We conclude that, in general, at this dose pyridostigmine is a safe drug for asthmatics; however, the distribution of individual results in this group cannot preclude the existence of a subpopulation of asthmatic patients who are more vulnerable to the effects of pyridostigmine.
AB - Respiratory function was evaluated in 12 healthy and 13 asthmatic volunteers following a single oral dose of pyridostigmine in a double-blind, placebo-controlled cross-over study. Respiratory function tests were performed at rest and after submaximal exercise at the time corresponding to the expected peak cholinesterase inhibition by pyridostigmine. A single dose of 60 mg pyridostigmine given to nonasthmatic subjects led to a decrease of 28.4% in cholinesterase activity when compared to the baseline and a statistically (but not physiologically) significant decrease in FEV1 (forced expiratory volume in 1 sec) both at rest (P<0.015) and after exercise (P<0.05). This effect showed a strong correlation to the degree of cholinesterase inhibition (r = -0.936, P<0.0001). According to these findings, a smaller dose of pyridostigmine (30 mg) was given to subjects with mild bronchial asthma. At that dose, pyridostigmine resulted in a similar inhibition of cholinesterase activity to a mean of 76.7% of the baseline. A significant decrease in the pulse rate was also found (P<0.005). However, no changes in respiratory function were observed when compared with the effects of placebo. The effect of post-exertion atropine inhalation on respiratory function was also unchanged with pyridostigmine at that dose. We conclude that, in general, at this dose pyridostigmine is a safe drug for asthmatics; however, the distribution of individual results in this group cannot preclude the existence of a subpopulation of asthmatic patients who are more vulnerable to the effects of pyridostigmine.
KW - Bronchial asthma
KW - Carbamates
KW - Persian gulf war
KW - Pulmonary function tests
KW - Pyridostigmine
UR - http://www.scopus.com/inward/record.url?scp=0026316189&partnerID=8YFLogxK
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AN - SCOPUS:0026316189
SN - 0021-2180
VL - 27
SP - 664
EP - 668
JO - Israel Journal of Medical Sciences
JF - Israel Journal of Medical Sciences
IS - 11-12
ER -