TY - JOUR
T1 - Neurotoxic effect of cisplatin and the cisplatin-procaine complex DPR studied in organotypic cultures of chick embryonic dorsal root ganglia
AU - Mandys, Vaclav
AU - Viale, Maurizio
AU - Vrana, Jiri
AU - Cafaggi, Sergio
AU - Esposito, Mauro
PY - 1998
Y1 - 1998
N2 - Neurotoxic effects of cisplatin and the cisplatin-procaine complex cis-diaminechloro-[2-(diethylamino)ethyl 4-amino-benzoate, N4]-chlorideplatinum(II) monohydrochloride monohydrate (DPR) were compared in organotypic cultures of chick embryonic dorsal root ganglia maintained in a semi-solid (soft agar) culture medium. The changes of two characteristics of the neurite outgrowth, the mean radial length of neuritic processes growing out from the ganglia and the area of neurite outgrowth around the ganglion, were used as parameters to evaluate the toxic effect of both compounds. The drugs were administered to the cultures at concentrations ranging from 13 to 120 μM. The half-maximum inhibition concentration (IC50) was determined from the concentration-response curves for both the mean radial length of neurites and the area of neurite outgrowth. An analysis of these parameters revealed that DPR was significantly less neurotoxic than cisplatin. In fact, considering the mean radial length of neurite processes, the IC50 of cisplatin were 56, 65 and 66 μM after 24, 48 and 72 h of exposure, respectively. By contrast, for DPR the IC50s were 116 μM after 24 h, and greater than 120 μM after 48 end 72 h of exposure. When we considered the area index (i.e. the area of neurite outgrowth normalized for the area of the ganglia), the IC50s for cisplatin were 41, 52 and 55 μM after 24, 48 and 72 h of exposure, respectively, whereas for DPR the IC50s were 59 μM after 24 h, and greater than 120 μM after 48 and 72 h of exposure. Our results support previous findings of lower toxicity of DPR to non-neoplastic tissues, as compared to cisplatin.
AB - Neurotoxic effects of cisplatin and the cisplatin-procaine complex cis-diaminechloro-[2-(diethylamino)ethyl 4-amino-benzoate, N4]-chlorideplatinum(II) monohydrochloride monohydrate (DPR) were compared in organotypic cultures of chick embryonic dorsal root ganglia maintained in a semi-solid (soft agar) culture medium. The changes of two characteristics of the neurite outgrowth, the mean radial length of neuritic processes growing out from the ganglia and the area of neurite outgrowth around the ganglion, were used as parameters to evaluate the toxic effect of both compounds. The drugs were administered to the cultures at concentrations ranging from 13 to 120 μM. The half-maximum inhibition concentration (IC50) was determined from the concentration-response curves for both the mean radial length of neurites and the area of neurite outgrowth. An analysis of these parameters revealed that DPR was significantly less neurotoxic than cisplatin. In fact, considering the mean radial length of neurite processes, the IC50 of cisplatin were 56, 65 and 66 μM after 24, 48 and 72 h of exposure, respectively. By contrast, for DPR the IC50s were 116 μM after 24 h, and greater than 120 μM after 48 end 72 h of exposure. When we considered the area index (i.e. the area of neurite outgrowth normalized for the area of the ganglia), the IC50s for cisplatin were 41, 52 and 55 μM after 24, 48 and 72 h of exposure, respectively, whereas for DPR the IC50s were 59 μM after 24 h, and greater than 120 μM after 48 and 72 h of exposure. Our results support previous findings of lower toxicity of DPR to non-neoplastic tissues, as compared to cisplatin.
KW - Cisplatin
KW - DPR
KW - Neurotoxicity
KW - Spinal ganglia
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U2 - 10.1097/00001813-199808000-00012
DO - 10.1097/00001813-199808000-00012
M3 - Article
C2 - 9773811
AN - SCOPUS:0031716321
VL - 9
SP - 659
EP - 663
JO - Anti-Cancer Drugs
JF - Anti-Cancer Drugs
SN - 0959-4973
IS - 7
ER -