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Lack of in Viva Binding to DNA of Piroctone olamine RPT1

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R 39 Lack of in Viva Binding to DNA of Piroctone-olamine P. Sagelsdorff, W.K. Lutz and Ch. Schlatter Institute Swiss F ederal Institute CH-8603 cf of Toxicology, and University Switzerland of Zzrich, Technology Schwerzenbach, Report prepared for HOiCHST PHARMA FORSCHUNG TOXIKOLOGIE Fostfach 80 03 2'0 am Maln 80 D-6320 Frankfurt Date Sept. of 16, isslre: 1983 DNA Binding Assay with Piroctone-olamine we 4 Materials and Methods Test compound. [6-14C)Piroctone-olamine monoethanolamine salt (I) (I-hydroxy-4-mlethylmonoethanolamine specific pyridone layer radioactivity ring. salt) 6-(2',4',4'-trimethylpentyl)-?(lH)-pyridone was of prepared 33.4 by the Hoechst radiolabel shown to (Merck) company with a the by thin mCi/mmol. purity The was was in be 98.5% with The radiochemical on polyamid vol.) chromatography 11 F,54 rats were between plates methanol/ethanolamine Animals. Kissleg, .held (No. libitum 4 per Young male (99+1 SPF Uistar weights cage obtained 150 were and from 170 Ivanovas, g. They were chow ad for FRG, ,with macrolone ranging on saw dust. Mijhle access They fed laboratory 71-343-7, and they Klingenthal had free AG, Kaiseraugst, to tap water for Switzerland) one week acclimatisation. Treatment. 50 % aqueous by The subcutaneous animais of 0.4 were 35 mg/kg b.w, (3.5 mCi/kg) (12 in single order in the vol.) hours to after under a teflon was mg/ml), to glass Piroctone-olamine, was simulate metabolism air the to administered 100% dermal cages a trap dissolved to three in rats l,?-propanediol injection placed absorption. where with an air stream l/min transported (I+4 48 exhaled collect the ether ethanolamine/methanol Isolation were were -. bled excised of chromatin. heart expired ['4C]O?. the The animals livers administration, anaesthesia. by open puncture in and homogenized at 4'C. Crude detergent [SageTsdorff ?O-30 ~'$000 Potter-Elvehjem-type prepared (BDH by precipitation Ltd., Poole homogenizer with the chromatin Nonidet et mg protein dpm/ml. non-ionic England) P 40 al., per Chemicals This pellet, was BH12 4NN, about . 3-3 1983]; containing the mg DNA and contained g liver, washed until Suspension DNA Binding Assay with Piroctone-olamine we 5 Isolation homogenized Urea in of DNA and further chromatin in a Waring pH 6.8. protein. blender The chromatin in 1 % (w/v) was pellet SDS, was 10 m M EDTA, with by 8 M 0.24 M Nazp04, The homogenate (CIP) column, deproteinized chloroform/isoamyl adsorption precipitation [Sagelsdorff protein) The amount was of on alcohol/phenol a hydroxylapatite with et a?., ethanol to and the dialysis, specific purified DNA was purified and repetitive radioactivity DNA (less succinate, of was than constant I983 2. The highly in 8 m M CaCl?, O.? "6: dissolved ?D m M sodium pH 6.0. 30 at performed counter analysis 2'60 DNA was determined of I mg DNA/ml. by assuming Scintillatjon in a Packard an absorbance counting scintillation nm for after Tricarb v' of a solution addition 460 CD, labelled Chromatin of 10 m l Insta-Gel equipped with and calibrated for the acetone The automatic samples. protein in was 1X (w/v) precipitated SDS (five with times). for the the Folin from from the CIP extract was The and redissolved to of last solution diluted amount Control together ccxnoarison of the 0.1 5 SDS and protein 1 ml was used with scintillation reagent. an untreated total to count show that counting. was determined (1) treated historical experiments. with with the DNA was isolated ones. animal - upon the held The respective - was used without external controls work-up with DNA samples was performed contamination radiolabels. (?) The chromatin incubated the first for chromatin animal. was pellet isolated at from the the liver of an untreated suoernatant from this the main rat of a in was 15 minutes 4OC with step of the net radiolabelled of the precipitation radioactivity from DNA preparation after in DNA only treated incubation exDeriment isolation The the DNA isolated vitro deducted all was DNA radioactivity into so that procedure radiolabel accounted introduced for. during the LAM ;ino:ng Assay Wlin Plroctone-o;mine page 6 Results and Discussion The injection respectively. 4 percent At and excretion amounted of to radiolabel 6+? percent within and 24 hours ?9_tlO arL bier in after in subcutaneous urine and faeces, additional respectively. the liver DNA percent, the Between and 24 percent ?4 and 48 hours were excreted administration and isolated the faeces, from results. Under the was activity converted in were to urine was this time for DNA and chromatin [14C]-labelling. at that the protein Table limit minute counted were 1 compiles of detection. The samples preliminary DNA-bound samples units Table for the of radiolabelled assumption this DNA radioactivity the specific and due of the to the DNA Piroctone-olamine were the divided 'Covalent by the Binding metabolites, dote administered Index, CBI', O.O?? molar to . as defined and 0.013 a footnote calculated 1 [Lutz, three 1979 J. Values treated rats. of 0.016, Radioactivity treated interactions the test with on the a radiolabelled of the test with DNA isolated substance compound DNA is in with from is an animal not necessarily Non-covalent the of that has due been to covalent of DNA. interaction of the compound experiments was unlikely th e third A more because column likely incorporation molecules the for is ['4CJ03 taken data Table respective that this control contribution given not is 1 show for the measurable. the biosynthetic to Such j14C;D,, reason of to observed if pool of that 6 of DNA radioactjvity the compound acid is radioactivity enter the degradable small is able case nucleic are the Table precursors. -lo yield obviously because, with the compounds caroon cegraoed purine.bases instance, from adenine the and guanine data on the a CO, molecule. after as exhaled amount not broken little within may as 0.01 48 2 surrunarizes of the exhalation On average, administration oercent . hours to inat in of the [14CJpiroctone-olamine. dose This radioactivity form of [14C JO?, administered extremely and was small does js be due mean during radiochemical the pyridone impurities moiety of administered ?iroctone-oiamine necessarily down metabolism. Due to the the fincing :hac the ;iLC,)Z, is formed in after the administration DNA must Control mignt in part of be with radiolabe?:ed samole, radioactivity due to biosynthetic incorporation 07 raaioiacel. Li4-? i,meIn2no; show :hzI this source of racioac:ivi:;/ experiments fui?y DNA Binding Asgay with Piroctone-olamine we 7 account biosynthetic for the DNA radioactivity: into liver Exhalation DNA were of ['4CJ0, and after oral incorporation iof 45 hIours ac'tivity 15 mg/kg after determined rats. administration from the liver specific b.w.['4Cjmethanol administration, to to male was clearly DNA isolated and radiolabelled of 4?B. The corresponded an apparent to 85% of CBI the corresponding radioactivity For and [:14CJexpiration dose, exhaied of the as accounted ['4C administered JO? within radioactivity 48 hours. [14C into expired an estimation relationship between JO, exhalation DNA, the ratio of was calculated liver DNA. biosynthetic DNA activity basis of of ratio range incorporation-of (CBI methanol the [14C]0, in units) data data specific on the , per to ('4CJ0, be 428:85% the = 503 for Multiplication with in the this obtained with Piroctone-olamine Index of about 0.05, in i.e. CBI resulted as the an apparent Binding same observed DNA radioactivities expressed units. Contamination observed the.protein that of DNA with but given protein in in protein could also contribute on the to the basis fact ci small of DNA radioactivity radioactivity of result the above a quantitative in the Table 1 is analysis conplicated of high by the activities precipitation must on presence molecules Based radioactivity is not due overestimations. it is highly probable of that the DNA results after but of detected to DNA binding ?rxursors protein. administration to biosynthetic [14CJPiroctone-olamine incorporation of ccntmination of radiclabelled the DNA with DNA synthesis and pernaps to If one disregards radioactivity as due . to on covalent low the above explanation hypothetically Piroctone-olamine with known for the the to origin values DNA, of given the The the in Table wculd 1 DNA and takes binding upon of figures strongest be extremely hepatocarcinogenic like :s >/inyl aflatoxjn ii0 comparison with carcinogens. initiating a CBI compounds 5:' or a genotoxi.c, exhibit mode of in the action, of dimethylnitrosamine, heparocarcinogens a CBI of a few order and i0'. chioride .!+? .fSerate s;‘ ~w such :-'I?. as The li ke l-acetyiaminofluorene nundrea, ana weak genotoxic to of carcinogens ieve? cf N,N-dimethyl-4-aminoazobenzene maximum possible is :oo DNA-binding low action. to consider bind zb'lity DNA on CgI ?irXzone-oizzl activity S.D.a Net activityS.D.b [dpmpl Specific [dpm/mg$! [CBI units? tl S.D. Control Cruae protein activity S.D. 0.4 kO.1 0 .C!S +0.005 Data chromatin [dpm/mgj 157 133 113 a The total variability (statistical counting error and fluctuations due to vial, scintillation cocktail, counter, external radiation) for a DNA sample containing little radioactivity was assumed tc be equal to the variability of DNA samples isolated from untreated animals held together with the treated ones. On the basis of 36 background a respective standard deviarion of 3.73 s:alues compiled for 12 years, cpm was calculated. The standard deviation for a net radioactivity in a vial therefore was taken as: 7 . : ~0.;3T+(().73,‘ \,,~ )? = 0.76 cpm - r.cl.n =‘ 5 The 'imit 2 ;evei The ,-?T zf of de:ect'cn 7 s-2 . The kindin ior radioactivity counting efficienfy Index Sauna appliE0 in a vial was 75% as: was calculate:! on c Ccvaient : $3:) is defined VI. piy] cnemicz iii;l? c I cnernlct; ?i$ / ma1 D!lA nuc?ecr:de ; Kg soay wslgnr 3.2-108 l CBI = dpm / mg DNA / kg booy neight DNA Binding A&say with Piroctone-olamine page 10 Table 7. Exhalation administration of ['4CJlabelled of CO;, after subcutaneous to 3 male rats [14CJPiroctone-olamine Period [h after of collection application] Cumulative Fraction Rat 1 of exhalation dose ? [10e5_! Rat 3 .o 4.6 a.4 11.0 13.0 3 Rat 2.8 3.6 6.1 8.0 9.7 o- 4 2.4 3.0 4.6 5.6 6.5 4 - 10 10 - 20 30 - 30 30 - 48

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