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Mehanizmi delovanja atrazina na steroidogenu aktivnost Leydig-ovih ćelija peripubertalnih pacova / The mechanism of atrazine action on steroidogenesis in peripubertal rat Leydig cells

<p>Rezultati prikazani u ovom radu opisuju efekte in vivo primene atrazina (2-hloro-4-<br />etilamino-6-izopropilamino-s-triazin) na ex vivo steroidogenezu u Leydig-ovim ćelijama<br />peripubertalnih pacova (tretiranih sa 50 mg/kg i 200 mg/kg telesne mase od 23. do 50.<br />dana starosti). Dobijeni rezultati jasno ukazuju da 28-dnevna in vivo primena atrazina<br />snažno inhibira testikularnu steroidogenezu, smanjujući ekspresiju gena za steroidogene<br />enzime i druge regulatorne proteine uključene u kontrolu testikularne steroidogeneze u<br />Leydig-ovim ćelijama peripubertalnih pacova. Rezultati in vivo primene atrazina<br />pokazuju da atrazin snažno inhibira ekspresiju gena za luteinizirajući hormon receptor<br />(LHR), skevendžer receptor-B1 (SR-B1), steroidogeni faktor-1 (SF-1), steroidogeni<br />akutni regulatorni protein (StAR), translokator protein (TSPO), fosfodiesterazu 4B,<br />3&beta;&minus;hidroksisteroid dehidrogenazu (&Eta;SD), CYP17A1 i 17&beta;HSD. Rezultati u okviru ovih<br />istraživanja pokazuju da primena atrazina tokom prepubertalnog perioda razvoja mužjaka<br />pacova dovodi do dozno-zavisnog smanjenja nivoa cAMP i snažne inhibicije androgeneze<br />u prisustvu hCG. Obzirom na blokadu ekspresije LHR, prvog elementa u aktivaciji<br />cAMP-signalnog puta, moglo bi se predpostaviti da je to uzrok blokade androgeneze kod<br />atrazinom-tretiranih životinja. Takođe, rezultati ukazuju na inhibiciju supstrat-stimulisane<br />produkcije androgena paralelno sa redukcijom ekspresije steroidogenih enzima CYP17A1<br />i 17&beta;HSD. U drugom delu ove doktorske disertacije, ispitivan je efekat direktne in vitro<br />primene različitih doza atrazina (1 nM, 1 &mu;M, 20 &mu;M, 50 &mu;M) na ekspresiju i aktivnost<br />steroidogenih enzima u kulturi preči&scaron;ćenih Leydig-ovih ćelija testisa peripubertalnih<br />pacova, pri čemu je zabeleženo stimulatorno dejstvo pomenutog herbicida. Naime,<br />zabeleženo je povećanje bazalne i hCG-stimulisane produkcije testosterona praćeno<br />povećanim nivoom cAMP u medijumu tretiranih ćelija. Pri ispitivanju ekspresije gena za<br />steroidogene enzime i regulatorne proteine, zabeleženo je povećanje ekspresije gena za<br />SF-1, StAR, CYP17A1 i 17&beta;HSD u hCG-stimulisanim uslovima. Takođe, povećana je i<br />produkcija testosterona nakon dodavanja progesterona i androstendiona kao supstrata,<br />kod Leydig-ovih ćelija tretiranih sa atrazinom. Da bi poku&scaron;ali da objasnimo za&scaron;to postoje<br />razlike u efektu atrazina u zavisnosti od načina primene, postavili smo jednokratni in vivo<br />eksperiment sa atrazinom (tretman sa 50 mg/kg i 200 mg/kg telesne mase, životinje<br />tretirane 50. dana starosti). Rezultati ovih eksperimenata ukazali su na up-regulaciju<br />testikularne steroidogeneze, kao i na povećan nivo cAMP kod životinja tretiranih sa<br />atrazinom Stoga, nivo cAMP se pojavljuje kao karika koja povezuje sva tri kori&scaron;ćena<br />eksperimentalna pristupa. Međutim, ostaje otvoreno pitanje na koji način atrazin utiče na<br />modulaciju nivoa cAMP i to pitanje predstavlja motiv za dalja istraživanja. Sumarno,<br />dobijeni rezultati ukazuju da 24-časovni tretman atrazinom izaziva povećanje, a<br />prolongirani tretman snažno smanjenje steroidogenog kapaciteta Leydig-ovih ćelija<br />peripubertalnih pacova.</p> / <p> In the present study, we investigated the effects of oral dosing of atrazine (2-chloro-4-<br /> ethylamino-6-isopropylamino-s-triazine) to peripubertal male rats (50 mg/kg and 200<br /> mg/kg body weight daily from postnatal day 23 to 50) on ex vivo Leydig cell<br /> steroidogenesis. Leydig cells from treated rats were characterised by significant decline in<br /> mRNA transcripts of several genes responsible for steroidogenesis: luteinizing hormone<br /> receptor (LHR), scavenger receptor-B1, steroidogenic acute regulatory protein (StAR),<br /> translocator protein, steroidogenic factor-1 (SF-1), phosphodiesterase 4B,<br /> 3&beta;&minus;hydroxysteroid dehydrogenase (&Eta;SD), CYP17A1 and 17&beta;HSD. In the presence of<br /> human chorion gonadotropin, the dose-dependent decrease in extra cellular cAMP level<br /> and accordingly strong inhibition of androgenesis were obtained. The transcription of<br /> LHR gene in Leydig cells of atrazine-treated rats was down-regulated in a dose-dependent<br /> manner, which could be the reason for reduction in cAMP level and expression of cAMPdependent<br /> genes. The results also indicated inhibition of substrate-stimulated androgen<br /> production in parallel with reduced expression of steroidogenih enzymes CYP17A1 and<br /> 17&beta;HSD. In the second part of this study we examined direct 24 h in vitro effect of<br /> different doses of atrazine (1 nM, 1 &mu;M, 20 &mu;M, 50 &mu;M) on expression and activity of<br /> steroidogenic enzymes in purified Leydig cells obtained from peripubertal rats. Obtained<br /> results indicated that 24 h-incubation of peripubertal Leydig cells in the presence of<br /> atrazine increased steroidogenic capacity of that cells. Increased basal and hCGstimulated<br /> testosterone production were accompanied by increasing levels of cAMP in the<br /> medium of treated cells. Also, in comparison to controls, gene expression revealed<br /> increased expression of SF-1, StAR, CYP17A1 and 17&beta;-HSD. When Leydig cells were<br /> challenged with progesterone and &Delta;4&ndash;androstenedione, testosterone production was<br /> increased in atrazine chalenged Leydig cells. To address these two opposite effects of<br /> atrazine we performed 24 h in vivo experiment in which peripubertal male rats (on<br /> postnatal day 50) were exposed to single atrazine treatment (50 mg/kg- and 200 mg/kgbody<br /> weight by gavage), and 24 h later, Leydig cells were isolated and testosterone levels<br /> in medium determined in basal and in hCG-stimulated conditions after 2 h-incubation<br /> period. Obtained results indicated that single in vivo exposure to atrazine was also<br /> accompanied 24 h later by up-regulation of Leydig cell androgenesis and increased cAMP<br /> level. According to the results obtained in this study, it seems that modulation of cAMP<br /> levels appear as a link that connects all three experimental approaches. However, the<br /> question of how atrazine affects the modulation of cAMP levels remains open, and<br /> present a motive for further research. In concluson, obtained results indicated that 24 h<br /> treatment with atrazine caused an increase, while prolonged treatment strongly reduce<br /> steroidogenic capacity of peripubertal Leydig cells.</p>

Identiferoai:union.ndltd.org:uns.ac.rs/oai:CRISUNS:(BISIS)81970
Date08 April 2010
CreatorsPogrmić Kristina
ContributorsKovačević Radmila, Kuhajda Ksenija, Kostić Tatjana, Cvijić Gordana
PublisherUniverzitet u Novom Sadu, Prirodno-matematički fakultet u Novom Sadu, University of Novi Sad, Faculty of Sciences at Novi Sad
Source SetsUniversity of Novi Sad
LanguageSerbian
Detected LanguageEnglish
TypePhD thesis
Formatapplication/pdf

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