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一些关于贝那普嗪(BRL 1288)的初步动物和人体药理学研究。

Some initial animal and human pharmacological studies with benapryzine (BRL 1288).

作者信息

Brown D M, Hughes B O, Marsden C D, Meadows J C, Spicer B

出版信息

Br J Pharmacol. 1973 Mar;47(3):476-86. doi: 10.1111/j.1476-5381.1973.tb08179.x.

Abstract
  1. The pA2 anti-acetylcholine activity in vitro for benapryzine was 6.55 compared with 9.02 for benzhexol.2. In vivo, the anti-acetylcholine activity of benapryzine relative to benzhexol was 0.038 as assessed by the mydriatic response of mice after subcutaneous administration. The relative activity assessed by the inhibition of pilocarpine-induced salivation was 0.13 after oral administration and 0.056 following subcutaneous administration of the drugs.3. Benapryzine had the same order of activity as benzhexol in inhibiting oxotremorine-induced tremors in mice.4. Benapryzine had anticonvulsant properties but no analgesic activity, whilst in high doses it antagonized the extrapyramidal symptoms induced by perphenazine in rats.5. In patients benapryzine was effective in reducing the symptoms of Parkinson's disease without overt anti-cholinergic effects or central hallucinogenic actions.6. Benapryzine abolished the excess tremor and reduced the rigidity and akinesia induced by physostigmine in Parkinsonian subjects.
摘要
  1. 贝那替秦体外抗乙酰胆碱活性的pA2值为6.55,而苯海索为9.02。

  2. 在体内,通过皮下给药后小鼠的散瞳反应评估,贝那替秦相对于苯海索的抗乙酰胆碱活性为0.038。口服给药后,通过抑制毛果芸香碱诱导的唾液分泌评估的相对活性为0.13,皮下给药后为0.056。

  3. 贝那替秦在抑制小鼠氧化震颤素诱导的震颤方面与苯海索具有相同的活性顺序。

  4. 贝那替秦具有抗惊厥特性但无镇痛活性,而高剂量时它可拮抗大鼠中奋乃静诱导的锥体外系症状。

  5. 在患者中,贝那替秦可有效减轻帕金森病症状,而无明显的抗胆碱能作用或中枢致幻作用。

  6. 贝那替秦消除了帕金森病患者由毒扁豆碱诱发的过度震颤,并减轻了僵硬和运动不能。

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本文引用的文献

1
The management of Parkinson's disease.帕金森病的管理
Arch Intern Med. 1959 Sep;104:439-68. doi: 10.1001/archinte.1959.00270090093017.
3
The metabolism and distribution of benapryzine.
Xenobiotica. 1971 Mar;1(2):169-77. doi: 10.3109/00498257109044388.
5
Objective measurement of parkinsonian tremor.
Lancet. 1965 Dec 18;2(7425):1278-9. doi: 10.1016/s0140-6736(65)92290-7.

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