Treatment | Mechanism tested | Concentration range tested | Brain region tested1-a | CNS neuron survival1-b | PC12 cell survival1-c | Referenced |
---|---|---|---|---|---|---|
Zaprinast | Type V PDE inhibitor | 1–300 μm | hpc | n | n | Maurice and Haslam, 1990 |
IBMX | General PDE inhibitor | 10–100 μm | hpc | n | y | Hartell, 1996 |
Milrinone | Type III PDE inhibitor | 10–100 μm | hpc | n | y | Marcoz et al., 1993 |
Trequinsin | General PDE inhibitor | 10 nm–10 μm | hpc | n | y | Sparwasser et al., 1994 |
8-CPT-cAMP | cAMP analog | 1–100 μm | str, hpc | n | y | Rydel and Greene, 1988 |
8-Br-cGMP | cGMP analog | 10 μm–10 mm | hpc | n | y | Farinelli et al., 1996a |
Adenosine | Ado receptor agonist | 1–300 μm | hpc | n | y | Zhang and Fredholm, 1994 |
Nitrobenzylthioinosine | Ado uptake blocker | 300 nm–100 μm | hpc | n | ? | Thorn and Jarvis, 1996 |
Propentofylline | Ado uptake blocker | 1–300 μm | hpc | n | ? | Zhang and Fredholm, 1994 |
Dilazep | Ado uptake blocker | 10 nm–100 μm | hpc | n | ? | Thorn and Jarvis, 1996 |
Verapamil | MDR inhibitor, Ca2+ channel blocker | 30 nm–300 μm | hpc | n | n | Ayesh et al., 1996 |
Cyclosporin A | MDR inhibitor, immunophilin | 3 nm–30 μm | ctx, hpc | n | n | Ayesh et al., 1996 |
Iloprost | Prostacyclin analog | 100 nm–10 μm | hpc | n | ? | Jackson et al., 1982 |
Indomethacin | Cyclooxygenase inhibitor | 3–300 μm | hpc | n | ? | Jackson et al., 1982 |
DIDS | Chloride transport inhibitor | 300 nm–100 μm | hpc | n | ? | Garcia and Lodish, 1989 |
Dideoxyforskolin | Chloride transport inhibitor | 30 nm–20 μm | hpc | n | ? | Sanchez-Olea et al., 1996 |
Flavopiridol | Cell cycle inhibitor, cdk inhibitor | 100–3 μm | hpc | n | y | Park et al., 1996 |
Ciclopirox olamine | Cell cycle inhibitor | 10 nm–3 μm | str, hpc | n | y | Farinelli and Greene, 1996 |
Actinomycin D | RNA synthesis inhibitor | 1–10 μm | hpc | n | y | Mesner et al., 1992 |
Cycloheximide | Protein synthesis inhibitor | 1 nm–10 μm | hpc | n | y/n | Furukawa et al., 1997 |
SNAP | Nitric oxide generator | 1–100 μm | ctx, hpc, str | n | y | Farinelli et al., 1996a |
DETA-NO | Nitric oxide generator | 1–100 μm | ctx, hpc, str | n | y | Farinelli et al., 1996a |
l-NAME | General NOS inhibitor | 10 μm–10 mm | hpc | n | n | Dawson et al., 1991 |
7-Nitroindazole | Neuronal NOS inhibitor | 100 nm–200 μm | hpc | n | n | O’Neill et al., 1996 |
Kynurenic acid | Glutamate receptor antagonist | 1 μm–10 mm | hpc | n | Zeevalk and Nicklas, 1989 | |
MK-801 | NMDA receptor antagonist | 100 nm–10 μm | hpc | n | n | Zeevalk and Nicklas, 1989 |
Insulin | Component of complete SFM | 25 μg/ml | hpc | n | y | di Porzio et al., 1980 |
Progesterone | Component of complete SFM | 20 nm | hpc | n | ? | di Porzio et al., 1980 |
Putrecine | Component of complete SFM | 60 μm | hpc | n | ? | di Porzio et al., 1980 |
Selenium | Component of complete SFM | 30 nm | hpc | n | ? | di Porzio et al., 1980 |
Transferrin | Component of complete SFM | 0.01–1 mg/ml | hpc | y | n | di Porzio et al., 1980 |
Dipyridamole | all | y | n |
8-Br-cGMP, 8-Bromo-cGMP; cdk, cyclin-dependent kinase; ctx, cortex; DIDS, 4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid; hpc, hippocampus; IBMX, 3-isobutyl-l-methylxanthine; n, no;l-NAME, Nω-nitro-l-arginine methyl ester; str, striatum; y, yes.
↵F1-a Brain regions from which the neurons were cultured and tested for this report.
↵F1-b Survival in MEM/F12 basal medium with indicated drug observed this study.
↵F1-c Survival of trophic factor-deprived PC12 cells as observed or reported by our laboratory; ? indicates not tested by us in PC12 cells.
F1-d Deontes either action of drug or action on PC12 cells.