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Reactivity of human iris-sphincter to muscarinic drugs in vitro.

作者信息

Patil P N

机构信息

Ohio State University, Division of Pharmacology, College of Pharmacy, Columbus 43210.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1992 Dec;346(6):614-9. doi: 10.1007/BF00168733.

DOI:10.1007/BF00168733
PMID:1484562
Abstract

From tissue to tissue the contractile response of human irides to carbachol varied by 40 fold. The mean EC50 value of carbachol in tissues remaining in an in vitro environment for 24-37 h was equal, however, to that obtained from tissues examined during 79-161 h. The maximum response of the tissue to the highest concentration of carbachol increased up to 24 h, then a gradual decline in the maximum occurred. In 38 observations, the average decline after 72 h was approximately 30%. A plot of negative log EC50 values (n = 38) of carbachol exhibited normal Gaussian curve. The geometric mean EC50 value of carbachol was 0.38 mumol/l (0.28-0.51 mumol/l, 95% C.L.). Based on EC50 values, the rank order of potency of cholinergic agonists is as follows: Muscarine = carbachol, 1 > pilocarpine, 1/5 > methacholine, 1/23 > bethanechol, 1/29 > acetylcholine, 1/1310. The percent maximum contraction of irides to muscarine, carbachol, pilocarpine, methacholine and bethanechol were 100, 100, 80, 76 and 95, respectively. Acetylcholine at the highest concentration tested produced 71% of the maximum produced by carbachol. Within a concentration range of 1 to 100 mumol/l, physostigmine consistently contracted isolated irides. The mean EC50 value was 6.73 mumol/l. The effect was sensitive to blockade by atropine. When the temperature of the bathing medium was lowered from 37.5 degrees C to 27.5 degrees C or 17.5 degrees C the magnitude and the duration of the response of the iris to carbachol was increased, the EC50 value, however, was not changed significantly. The response to pilocarpine was similarly altered by the lower temperature.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

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本文引用的文献

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THE UPTAKE OF ATROPINE AND RELATED DRUGS BY INTESTINAL SMOOTH MUSCLE OF THE GUINEA-PIG IN RELATION TO ACETYLCHOLINE RECEPTORS.豚鼠肠道平滑肌对阿托品及相关药物的摄取与乙酰胆碱受体的关系
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Some quantitative uses of drug antagonists.
人类、白化兔和有色兔虹膜开大肌中节后α-肾上腺素能受体的比较。
Naunyn Schmiedebergs Arch Pharmacol. 1996 Dec;354(6):765-72. doi: 10.1007/BF00166903.
4
Cholinergic sensitivity of irides from donors with various pathological conditions and lens implants.患有各种病理状况及植入晶状体的供体虹膜的胆碱能敏感性。
Naunyn Schmiedebergs Arch Pharmacol. 1992 Dec;346(6):620-8. doi: 10.1007/BF00168734.
药物拮抗剂的一些定量应用。
Br J Pharmacol Chemother. 1959 Mar;14(1):48-58. doi: 10.1111/j.1476-5381.1959.tb00928.x.
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Muscarinic receptors of rabbit irides.兔虹膜的毒蕈碱受体
Naunyn Schmiedebergs Arch Pharmacol. 1983 Mar;322(2):104-10. doi: 10.1007/BF00512382.
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Interaction of melanin with oxygen.黑色素与氧气的相互作用。
Arch Biochem Biophys. 1980 Mar;200(1):140-8. doi: 10.1016/0003-9861(80)90340-9.
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Clinical pharmacokinetics of the eye. Proctor lecture.
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Adrenergic receptors of the bovine iris sphincter.牛虹膜括约肌的肾上腺素能受体。
J Pharmacol Exp Ther. 1969 Apr;166(2):299-307.
8
A study of the cholinergic and ganglionic-stimulant drugs on the isolated bovine iris sphincter.关于胆碱能和神经节兴奋剂对离体牛虹膜括约肌作用的研究。
Arch Int Pharmacodyn Ther. 1971 Apr;190(2):249-60.
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The pharmacological differentiation of adrenergic receptors.肾上腺素能受体的药理学分化
Ann N Y Acad Sci. 1967 Feb 10;139(3):553-70. doi: 10.1111/j.1749-6632.1967.tb41229.x.
10
Log-normal distribution of equiefective doses of norepinephrine and acetylcholine in several tissues.去甲肾上腺素和乙酰胆碱在多个组织中的等效剂量的对数正态分布。
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