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Do local vasomotor effects elicit the motor deficits induced by intrathecally applied substance P antagonists in the rat?

作者信息

Barber A, Wild A, Wedel R

机构信息

Department of Pharmacology, Biological Research, E. Merck Darmstadt, F.R.G.

出版信息

Neurosci Lett. 1987 Sep 23;80(2):219-23. doi: 10.1016/0304-3940(87)90657-4.

Abstract

The intrathecal application of the substance P (SP) antagonists [D-Pro2,D-Trp7,9]SP (DPDT) and [D-Arg1, D-Pro2, D-Trp7,9, Leu11]SP (DAPTL) to the lumbar region of intact, freely moving rats produced laming of the hindlimbs at doses of 0.375 nmol and above, and 1.5 nmol and above, respectively. In addition, the administration of DPDT (doses of 25 and 0.18 nmol) and DAPTL (25 and 0.6 nmol) produced a powerful constriction of the dorsal median spinal vein (DMSV) in decerebrated, unanaesthetised rats. Intrathecal SP (25 or 1.0 nmol) had a similar action on the spinal circulation to DPDT and DAPTL, though laming was first observed at doses of 30 nmol and higher. This suggests that intrathecally applied SP antagonists do not elicit laming by causing an obstruction of the venous drainage of the spinal cord. Disturbances of the spinal circulation could, however, influence the results of behavioural or physiological experiments in which SP or its analogues are administered intrathecally.

摘要

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