Objective and design:
Astrocytes actively participate in the inactivation of neurotransmitters. In this work we elucidated the contribution of astrocytes in clearance of histamine, a process which has not yet been fully clarified.
The characteristics of [3H]-histamine uptake were determined in cultured neonatal rat type 1 astrocytes and histamine-N-methyl-transferase expression was determined using RT-PCR.
These cells transport [3H]-histamine in a time- and concentration-dependent manner. The histamine clearance by astrocytes was described by a mathematical model including two processes: electrodiffusion and active transport. A further analysis of kinetic parameters of a carrier-operated transport revealed a single transport system with Michaelis constant (Km) of 3.5 ± 0.8 μM and a maximal uptake rate (Vmax) of 7.9 ± 0.3 pmol/mg protein/min. From drugs tested amitriptyline, desipramine, mepyramine and cimetidine significantly decreased [3H]-histamine uptake. Taken-up histamine could be metabolically degraded in cultured astrocytes, since they express mRNA for enzyme histamine-N-methyltransferase.
Astrocytes participate in the clearance of extracellular histamine by electrodiffusion and active transport by a yet not identified carrier. Taken up histamine can be converted to tele-methylhistamine within astrocytes thus indicating the involvement of astrocytes not only in clearance but also in the inactivation of histamine.
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Received 24 November 2007; returned for revision 4 January 2008; received from final revision 22 May 2008; accepted by A. Falus 3 November 2008
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Osredkar, D., Burnik-Papler, T., Pečavar, B. et al. Kinetic and pharmacological properties of [3H]-histamine transport into cultured type 1 astrocytes from neonatal rats. Inflamm. Res. 58, 94–102 (2009). https://doi.org/10.1007/s00011-009-8103-4
- Histamine uptake
- Histamine electrodiffusion