Adenosine modulates methylmercuric chloride (MeHgCl)-inducedd-aspartate release from neonatal rat primary astrocyte cultures

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Title: Adenosine modulates methylmercuric chloride (MeHgCl)-inducedd-aspartate release from neonatal rat primary astrocyte cultures
Authors: Aschner, M., Mullaney, K.J., Wagoner, D.E., Lash, L.H., Kimelberg, H.K.
Source: Brain Research; August 1995, Vol. 689 Issue: 1 p1-8, 8p
Abstract: The effects of adenosine, and selective adenosine receptor agonists and antagonists on methylmercury (MeHg)-induced aspartate release were studied in neonatal rat primary astrocyte cultures. Whereas basal levels ofd-[3H]aspartate release were unchanged upon treatment with adenosine or selective A1 receptor agonists, N6-cyclopentyladenosine (CPA), cyclohexyladenosine (CHA), and R-phenylisopropyladenosine (R-PIA), all partially reversed the MeHg-induced release ofd-aspartate. Treatment of astrocytes with the xanthine derivative, theophylline, an adenosine antagonist, reversed the inhibitory effect of adenosine on MeHg-inducedd-[3H]aspartate release. Since the effect of MeHg ond-[3H]aspartate release is known to be associated with sulfhydryl (-SH) groups which are controlled by intracellular glutathione concentrations [GSH]i, we also evaluated the effects of adenosine, the A1 agonists CPA and CHP, and the adenosine antagonist, theophylline, on astrocytic [GSH]i. Attenuation of the stimulatory effect of MeHg ond-[3H]aspartate release by adenosine and its agonists occurred in the presence of reduced astrocytic [GSH]i, suggesting that other mechanisms must be invoked for this protective effect. Whilst the mechanism of MeHg-inducedd-[3H]aspartate release is not known, the data suggest a role for adenosine in its regulation.
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  Data: Adenosine modulates methylmercuric chloride (MeHgCl)-inducedd-aspartate release from neonatal rat primary astrocyte cultures
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  Data: <searchLink fieldCode="AR" term="%22Aschner%2C+M%2E%22">Aschner, M.</searchLink><br /><searchLink fieldCode="AR" term="%22Mullaney%2C+K%2EJ%2E%22">Mullaney, K.J.</searchLink><br /><searchLink fieldCode="AR" term="%22Wagoner%2C+D%2EE%2E%22">Wagoner, D.E.</searchLink><br /><searchLink fieldCode="AR" term="%22Lash%2C+L%2EH%2E%22">Lash, L.H.</searchLink><br /><searchLink fieldCode="AR" term="%22Kimelberg%2C+H%2EK%2E%22">Kimelberg, H.K.</searchLink>
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  Data: Brain Research; August 1995, Vol. 689 Issue: 1 p1-8, 8p
– Name: Abstract
  Label: Abstract
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  Data: The effects of adenosine, and selective adenosine receptor agonists and antagonists on methylmercury (MeHg)-induced aspartate release were studied in neonatal rat primary astrocyte cultures. Whereas basal levels ofd-[3H]aspartate release were unchanged upon treatment with adenosine or selective A1 receptor agonists, N6-cyclopentyladenosine (CPA), cyclohexyladenosine (CHA), and R-phenylisopropyladenosine (R-PIA), all partially reversed the MeHg-induced release ofd-aspartate. Treatment of astrocytes with the xanthine derivative, theophylline, an adenosine antagonist, reversed the inhibitory effect of adenosine on MeHg-inducedd-[3H]aspartate release. Since the effect of MeHg ond-[3H]aspartate release is known to be associated with sulfhydryl (-SH) groups which are controlled by intracellular glutathione concentrations [GSH]i, we also evaluated the effects of adenosine, the A1 agonists CPA and CHP, and the adenosine antagonist, theophylline, on astrocytic [GSH]i. Attenuation of the stimulatory effect of MeHg ond-[3H]aspartate release by adenosine and its agonists occurred in the presence of reduced astrocytic [GSH]i, suggesting that other mechanisms must be invoked for this protective effect. Whilst the mechanism of MeHg-inducedd-[3H]aspartate release is not known, the data suggest a role for adenosine in its regulation.
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        Value: 10.1016/0006-8993(95)00496-D
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        Text: English
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              Text: August 1995
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