Excitatory amino acids, monoamine, and nitric oxide synthase systems in organotypic cultures: biochemical and immunohistochemical analysis

• Published in: Amino acids Vol. 19; no. 1; pp. 33 - 43
• Main Authors: Herrera-Marschitz, M, Kohlhauser, C, Gomez-Urquijo, S, Ubink, R, Goiny, M, Hökfelt, T
• Format: Journal Article Conference Proceeding
• Language: English
• Published: Austria Springer Nature B.V 01.01.2000
• Subjects: Amino acids; Animals; Biochemical analysis; Biogenic Monoamines - metabolism; Brain; Brain - enzymology; Brain - metabolism; Caudate-putamen; Cell culture; Cortex (cingulate); Dendrites; Dopamine; Excitatory amino acids; Excitatory Amino Acids - metabolism; Glutamine; High-performance liquid chromatography; Hydroxylase; Immunohistochemistry; Medicin och hälsovetenskap; Mesolimbic system; Neonates; Neostriatum; Nerve endings; Neurons; Nitric oxide; Nitric Oxide Synthase - metabolism; Nitric-oxide synthase; Organ Culture Techniques; Rats; Rats, Sprague-Dawley; Substantia nigra; Tyrosine; Tyrosine 3-monooxygenase; Ventral tegmentum
• ISSN: 0939-4451; 1438-2199
• DOI: 10.1007/s007260070031

The nigrostriatal and mesolimbic systems of the rat have been re-constructed using the organotypic culture model, whereby neonatal brain tissue is grown in vitro for approximately one month. The nigrostriatal cultures consisted of tissue from the substantia nigra, dorsal striatum and frontoparietal cortex; while the mesolimbic cultures included the ventral tegmental area, ventral striatum and cingulate cortex. The cultures were grown at 35 degrees C in normal atmosphere, using a tuberoller device placed in a cell incubator and changing the medium every 3-4 days. The in vitro development was evaluated with an inverted microscope equipped with a variable relief contrast function. Samples were taken directly from the medium in the culture tube and analysed for several amino acids with HPLC. After a month the cultures were fixed and processed for immunohistochemistry. High levels of glutamate and aspartate were observed every time the medium was changed, but the levels rapidly decreased reaching a steady state after approximately 24h. A decrease in the levels was also observed along development, reaching stable values (approximately 2 microM and approximately 0.12 microM for glutamate and aspartate, respectively) at approximately two weeks, but only when the cultures showed an apparently healthy development. The levels were approximately 10 times higher in deteriorating or apparently damaged cultures. Glutamine levels were in the mM range and remained stable along the entire experiment. No differences were observed among nigrostriatal and mesolimbic cultures. Immunohistochemistry confirmed the impressions obtained from microscopic and biochemical analysis along the in vitro development, revealing apparently healthy neuronal systems with characteristics similar to those observed in vivo, when tyrosine hydroxylase and nitric oxide synthase, markers for dopamine and nitric oxide containing neurons, respectively, were analysed. In the substantia nigra, nitric oxide synthase-positive networks surrounded tyrosine hydroxylase-positive neurons, while in the striatum nitric oxide synthase dendrites were surrounded by tyrosine hydroxylase-positive nerve terminals, suggesting a reciprocal interaction among dopamine and nitric oxide containing neurons. Thus, the organotypic model appears to capture many of the neurochemical and morphological features seen in vivo, providing a valuable model for studying in detail the neurocircuitries of the brain.