Literature DB >> 1330188

Lack of effect of the antimigraine drugs, sumatriptan, ergotamine and dihydroergotamine on arteriovenous anastomotic shunting in the dura mater of the pig.

M O den Boer1, J A Somers, P R Saxena.   

Abstract

1. In anaesthetized animals, the antimigraine drugs, sumatriptan, ergotamine and dihydroergotamine, reduce carotid arteriovenous anastomotic shunting. Within the carotid vascular bed arteriovenous anastomoses are located, amongst other places in the dura mater, which is a putative site of the pain during a migraine attack. 2. In this investigation, we have localized and measured the arteriovenous shunting within the carotid vascular bed of the pig by using simultaneous intracarotid injections of radiolabelled microspheres of three different sizes (10, 15 and 50 microns), which provides an index of blood flow via arteriovenous anastomoses larger than approximately 14, 27 and 90 microns diameter, respectively. The effects of sumatriptan (0.3 mg kg-1), ergotamine (0.02 mg kg-1), dihydroergotamine (0.1 mg kg-1) and saline were studied by repeating the injections of 15 and 50 microns spheres after the treatments. 3. There was no difference in shunting or entrapment between the 10 and 15 microns microsphere, indicating the absence of arteriovenous anastomoses with a diameter between 14 and 27 microns. 4. Arteriovenous anastomoses with a diameter between 27 and 90 microns, as indicated by the difference in blood flow measured by 15 and 50 microns spheres, were located in the dura mater, ears, skin, fat and, to a lesser extent, in the skeletal muscles and eyes. 5. Sumatriptan, ergotamine and dihydroergotamine reduced the overall flow in the smaller arteriovenous anastomoses (diameter between 27 and 90 microns), and even more in larger shunts (wider than 90 microns). 6. Locally, blood flow in the smaller arteriovenous shunts was reduced in the skin and fat, but not in the dura mater, ears, eyes and muscles.It is not possible to determine in which tissues blood flow in the larger arteriovenous anastomoses was reduced.7. Tissue blood flow measured with 15 gm microspheres remained unchanged after the three antimigraine drugs, implying a lack of effect on capillary flow.8. It is concluded that in the anaesthetized pigs the only evident effect of these antimigraine drugs on carotid haemodynamics is a decrease in blood flow in both smaller and larger arteriovenous anastomoses;the smaller arteriovenous anastomoses were affected in the skin and fat, but not in other tissues.

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Year:  1992        PMID: 1330188      PMCID: PMC1907860          DOI: 10.1111/j.1476-5381.1992.tb12786.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  28 in total

1.  Carotid vascular effects of ergotamine and dihydroergotamine in the pig: no exclusive mediation via 5-HT1-like receptors.

Authors:  M O den Boer; J P Heiligers; P R Saxena
Journal:  Br J Pharmacol       Date:  1991-09       Impact factor: 8.739

2.  Vascular responses of dura mater.

Authors:  F M Faraci; K A Kadel; D D Heistad
Journal:  Am J Physiol       Date:  1989-07

3.  Neurogenically mediated plasma extravasation in dura mater: effect of ergot alkaloids. A possible mechanism of action in vascular headache.

Authors:  S Markowitz; K Saito; M A Moskowitz
Journal:  Cephalalgia       Date:  1988-06       Impact factor: 6.292

4.  The macro and microvasculature of the dura mater.

Authors:  C W Kerber; T H Newton
Journal:  Neuroradiology       Date:  1973-12       Impact factor: 2.804

5.  Diameter of arterial microvessels trapping 8--10 micron, 15 micron and 25 micron microspheres as determined by vital microscopy of the hamster cheek pouch.

Authors:  W H Dickhoner; B R Bradley; G S Harell
Journal:  Invest Radiol       Date:  1978 Jul-Aug       Impact factor: 6.016

6.  Computer programs for the radioactive microsphere technique. Determination of regional blood flows and other haemodynamic variables in different experimental circumstances.

Authors:  P R Saxena; H C Schamhardt; R P Forsyth; J Hoeve
Journal:  Comput Programs Biomed       Date:  1980-12

7.  The antimigraine drug, sumatriptan (GR43175), selectively blocks neurogenic plasma extravasation from blood vessels in dura mater.

Authors:  M G Buzzi; M A Moskowitz
Journal:  Br J Pharmacol       Date:  1990-01       Impact factor: 8.739

8.  Timing and topography of cerebral blood flow, aura, and headache during migraine attacks.

Authors:  J Olesen; L Friberg; T S Olsen; H K Iversen; N A Lassen; A R Andersen; A Karle
Journal:  Ann Neurol       Date:  1990-12       Impact factor: 10.422

9.  Reduction of cephalic arteriovenous shunting by ergotamine is not mediated by 5-HT1-like or 5-HT2 receptors.

Authors:  A H Bom; J P Heiligers; P R Saxena; P D Verdouw
Journal:  Br J Pharmacol       Date:  1989-06       Impact factor: 8.739

10.  Ergotamine-induced constriction of cranial arteriovenous anastomoses in dogs pretreated with phentolamine and pizotifen.

Authors:  P R Saxena; N A Koedam; J Heiligers; R P Hof
Journal:  Cephalalgia       Date:  1983-06       Impact factor: 6.292

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  4 in total

1.  Effects of current and prospective antimigraine drugs on the porcine isolated meningeal artery.

Authors:  Suneet Mehrotra; Saurabh Gupta; Ingrid M Garrelds; Carlos M Villalón; Pramod R Saxena; Ad J J C Bogers; Antoinette Maassenvandenbrink
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2006-11-14       Impact factor: 3.000

2.  NG-nitro L-arginine methyl ester: systemic and pulmonary haemodynamics, tissue blood flow and arteriovenous shunting in the pig.

Authors:  E M van Gelderen; M O Den Boer; P R Saxena
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1993-10       Impact factor: 3.000

3.  Inhibition of nitric oxide biosynthesis and carotid arteriovenous anastomotic shunting in the pig.

Authors:  E M van Gelderen; P R Saxena
Journal:  Br J Pharmacol       Date:  1994-03       Impact factor: 8.739

4.  The effect of nitric oxide donors on haemodynamics and blood flow distribution in the porcine carotid circulation.

Authors:  E M van Gelderen; E L De Bruijne; H J Agteresch; P R Saxena
Journal:  Br J Pharmacol       Date:  1995-03       Impact factor: 8.739

  4 in total

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