Farmacologia Reprodução - Golan (3 Ed)
Farmacologia Reprodução - Golan (3 Ed)
Farmacologia Reprodução - Golan (3 Ed)
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Introdução e Caso
Fisiologia dos hormônios da reprodução
Síntese de progestágenos, andrógenos e estrógenos
Ação e metabolismo hormonais
Eixo hipotálamo-hipófise-gônadas
Integração do controle endócrino | Ciclo menstrual
Fisiopatologia
Ruptura do eixo hipotálamo-hipófise-gônadas
Crescimento inapropriado de tecidos hormônio-dependentes
Secreção diminuída de estrógenos ou andrógenos
Classes e agentes farmacológicos
Inibidores dos hormônios gonadais
Inibidores de síntese
Antagonistas de receptores
Hormônios e análogos hormonais | Contracepção
Contraceptivos combinados (associações de estrógeno-progestágeno)
Contracepção apenas com progestágenos
Contracepção de emergência (do dia seguinte)
Contracepção masculina
Hormônios e análogos hormonais | Reposição
Estrógenos e progestágenos
Andrógenos
Conclusão e perspectivas
Leiturasugerida
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CASO
Amy J percebeu que, pela primeira vez, seus cabelos estavam ficando mais finos durante sua adolescência. Apesar da ocorrência de certa queda dos cabelos,
Srta. J constatou, por outro lado, crescimento excessivo de pelos no rosto; algumas vezes, foi até mesmo obrigada a usar um barbeador para retirar pelos
inconvenientes. Aos 24 anos, procurou o médico e queixou-se do problema relacionado com o excesso de pelos, bem como de seu ciclo menstrual irregular. Na
anamnese, o médico descobriu que o maior intervalo de tempo entre os ciclos menstruais foi de 6 meses, enquanto o mais curto foi de 22 dias. Quando Srta. J
menstrua, o fluxo é intenso e dura mais que a média anterior de 5 dias. O crescimento anormal de pelos no rosto dela, nos membros, no abdome e nas
mamas começou por volta dos 15 anos de idade. Srta. J também relatou que estava acima do peso normal desde a faculdade, embora fosse muito ativa no
ensino médio, jogando futebol e nadando. O médico solicitou vários testes, cujos resultados revelaram níveis ligeiramente elevados de testosterona livre e
total e aumento da relação entre níveis plasmáticos de LH e FSH.
Com base nesses achados, o médico diagnosticou que a paciente provavelmente apresentava um distúrbio denominado síndrome do ovário policístico
(SOPC). Recomendou o uso de anticoncepcionais orais combinados para regularizar o ciclo menstrual e prescreveu também espironolactona para reduzir os
problemas relacionados com crescimento de pelos e calvície.
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1. Qual é a ligação fisiopatológica entre crescimento excessivo de pelos e infertilidade na síndrome do ovário policístico?
2. Por que foi prescrita espironolactona para o problema capilar de Srta. J?
3. Como agem os contraceptivos orais e como podem ajudar a regular os ciclos menstruais de Srta. J?
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FIGURA 29.1 Síntese de progestágenos, andrógenos e estrógenos. Progestágenos, andrógenos e estrógenos são hormônios
esteroides derivados do colesterol. Os principais progestágenos incluem progesterona e 17α-hidroxiprogesterona. Andrógenos incluem
desidroepiandrosterona (DHEA), androstenediona e testosterona. Estrógenos, que incluem estrona e estradiol, são formas aromatizadas
de seus andrógenos conjugados: androstenediona é aromatizada a estrona, enquanto testosterona é aromatizada a estradiol. Tanto
estradiol quanto estrona são metabolizados a estriol, estrógeno fraco (não ilustrado). Algumas das relações precursor-produto entre os
hormônios foram omitidas para maior clareza (ver também Figura 28.2). HSD = hidroxiesteroide desidrogenase.
FIGURA 29.2 Conversão intracelular de testosterona a di-hidrotestosterona. Testosterona circula no plasma ligada a
globulina de ligação de hormônios sexuais (SHBG) e albumina (não ilustrada). A testosterona livre difunde-se pela membrana plasmática
das células para o citosol. Em tecidos-alvo, a enzima 5α-redutase converte testosterona em di-hidrotestosterona, que apresenta
atividade androgênica aumentada em comparação com testosterona. Di-hidrotestosterona liga-se com alta afinidade ao receptor de
andrógeno, formando um complexo que é transportado até o núcleo. Homodímeros de di-hidrotestosterona e receptor de andrógeno
iniciam a transcrição de genes dependentes de andrógeno. Finasterida e dutasterida, fármacos utilizados no tratamento de hipertrofia
prostática benigna e queda de cabelo de padrão masculino, inibem a enzima 5α-redutase.
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FIGURA 29.4 Sistemas de duas células para a ação dos hormônios gonadais. No homem, a ligação de hormônio luteinizante
(LH) ao receptor de LH (LH-R) ativa a síntese de testosterona em células de Leydig. A seguir, testosterona difunde-se para as células de
Sertoli adjacentes, onde a ligação do hormônio foliculoestimulante (FSH) a seu receptor (FSH-R) aumenta os níveis da proteína de
ligação de andrógenos (ABP). ABP estabiliza as concentrações elevadas de testosterona que, juntamente com outras proteínas induzidas
por FSH e sintetizadas nas células de Sertoli, promovem a espermatogênese no epitélio germinativo adjacente (não ilustrado). Na
mulher, LH atua de modo análogo, promovendo a síntese de andrógeno (androstenediona) nas células da teca. A seguir, o andrógeno se
difunde para as células granulosas vizinhas, onde a aromatase converte androstenediona em estrona, que é, então, reduzida a estrógeno
biologicamente ativo, o estradiol. FSH aumenta a atividade da aromatase nas células granulosas, promovendo a conversão de
andrógeno em estrógeno. Observe que a di-hidrotestosterona não é substrato da aromatase.
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FIGURA 29.5 O ciclo menstrual. O ciclo menstrual é dividido em fase folicular e fase lútea. A ovulação define a transição entre essas
duas fases. Durante a fase folicular, as células gonadotróficas da adeno-hipófise secretam LH e FSH em resposta à estimulação pulsátil de
GnRH. LH e FSH circulantes promovem crescimento e maturação dos folículos ovarianos. Folículos em desenvolvimento secretam
quantidades crescentes de estrógeno. A princípio, o estrógeno exerce efeito inibidor sobre a liberação de gonadotrofinas. Entretanto,
imediatamente antes da metade do ciclo menstrual, o estrógeno exerce breve efeito de retroalimentação positiva sobre a liberação de
LH e FSH. Isso é seguido de ruptura do folículo e liberação de um óvulo na tuba uterina. Durante a segunda metade do ciclo, o corpo
lúteo secreta tanto estrógeno
s rógeno quanto progesterona.
est s erona. Progesterona induz alteração de endométrio, que passa de tipo proliferativo para
progest
secretor. Se não houver fertilização nem implantação de um blastocisto dentro de 14 dias após a ovulação, corpo lúteo involui, secreção
de estrógeno e progesterona declina, ocorre menstruação e começa um novo ciclo.
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TABELA 29.1 Mecanismos gerais dos distúrbios do trato reprodutor para os quais são utilizados agentes farmacológicos.
Mecanismo Exemplos
Câncer de mama
Hipogonadismo
Secreção diminuída de estrógeno ou andrógeno
Menopausa
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FIGURA 29.6 Modulação farmacológica da ação de hormônios gonadais. A modulação farmacológica da ação de hormônios
gonadais pode ser dividida em inibidores da síntese hormonal e antagonistas dos receptores hormonais. A administração contínua de
GnRH suprime a liberação de LH e FSH pela adeno-hipófise, impedindo, assim, a síntese de hormônios gonadais. Antagonistas do receptor
de GnRH (cetrorrelix, ganirrelix) também são utilizados para esse propósito. Finasterida e dutasterida inibem a enzima 5α-redutase,
impedindo, portanto, a conversão da testosterona em di-hidrotestosterona mais ativa. Inibidores da aromatase (exemestano,
formestano, anastrozol, letrozol) inibem a produção de estrógenos a partir de andrógenos. Diversos antagonistas dos receptores
hormonais e moduladores impedem a ação de estrógenos endógenos (alguns MSRE), andrógenos (flutamida, espironolactona) e
progesterona (mifepristona).
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TABELA 29.2 Atividade agonista e antagonista tecidual específica de moduladores seletivos dos receptores de estrógeno (MSRE).
Tamoxifeno – + +
Raloxifeno – – ++
Estrógeno, o hormônio fisiológico, apresenta efeitos estimuladores em mama, endométrio e osso. Tamoxifeno é antagonista no tecido mamário e, por conseguinte, é utilizado no
tratamento do câncer de mama positivo para receptor de estrógeno. Raloxifeno, o MSRE mais recente, atua como agonista no osso, porém como antagonista em mama e
endométrio. Raloxifeno foi aprovado para prevenção e tratamento de osteoporose em mulheres pós-menopáusicas. Clomifeno (não consta da tabela) é MSRE que atua como
antagonista dos receptores de estrógeno em hipotálamo e adeno-hipófise; é utilizado clinicamente para aumentar a secreção de FSH e induzir, portanto, a ovulação.
FIGURA 29.7 Modelo para a especificidade tecidual de ação dos MSRE. Os MSRE exibem atividade antagonista ou agonista
parcial nos receptores de estrógeno, que é específica do tecido. Essa especificidade de ação em nível tecidual parece ser explicada pelas
seguintes observações: (1) coativadores e/ou correpressores da transcrição são expressos de modo específico em nível tecidual; (2) o
complexo MSRE-receptor de estrógeno (RE) pode associar-se a alguns coativadores ou correpressores, mas não a outros; e (3) pode haver
ativação ou inibição de genes por diferentes combinações de MSRE-RE e coativadores ou correpressores. No exemplo apresentado, supõe-
se que as células ósseas expressem coativadores (cofatores) X e Y, enquanto as células mamárias só expressem o coativador Y. O complexo
estrógeno–RE pode associar-se a X e Y, enquanto o complexo MSRE-RE pode associar-se apenas a X. A. Nas células ósseas, a ligação de
estrógeno a RE e o recrutamento de coativadores X e Y induzem a expressão dos genes 1, 2 e 3. O complexo MSRE-RE não pode ligar-se ao
coativador Y, e o complexo MSRE-RE-cofator X induz apenas a expressão do gene 1. No osso, portanto, estrógeno é agonista pleno,
enquanto MSRE é agonista parcial. B. Nas células mamárias, a ligação de estrógeno a RE e o recrutamento do coativador Y induz a
expressão do gene 2, porém MSRE é incapaz de promover a expressão de qualquer gene. Na mama, portanto, MSRE atua como
antagonista. Para maior simplicidade, esse modelo só mostra coativadores, embora correpressores também estejam envolvidos na ação
dos MSRE.
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GHPDPD7DPR[LIHQRYHPVHQGRXWLOL]DGRQRWUDWDPHQWRSDOLDWLYRGRFkQFHUGHPDPDPHWDVWiWLFRH
FRPRWHUDSLDDGMXYDQWHDSyVQRGXOHFWRPLD2WDPR[LIHQRpDQWDJRQLVWDGRVUHFHSWRUHVGHHVWUyJHQR
QRWHFLGRPDPiULRSRUpPDJRQLVWDSDUFLDOHPHQGRPpWULRHRVVR(VVHVHIHLWRVIDUPDFRGLQkPLFRV
UHVXOWDP HP LQLELomR GR FUHVFLPHQWR GR FkQFHU GH PDPD GHSHQGHQWH GH HVWUyJHQR PDV WDPEpP QD
HVWLPXODomR GR FUHVFLPHQWR HQGRPHWULDO (P FRQVHTXrQFLD GHVWH ~OWLPR HIHLWR D DGPLQLVWUDomR GH
WDPR[LIHQRHVWiDVVRFLDGDDDXPHQWRGHTXDWURDVHLVYH]HVQDLQFLGrQFLDGHFkQFHUHQGRPHWULDO3RU
FRQVHJXLQWH SDUD PLQLPL]DU R ULVFR GH FkQFHU HQGRPHWULDO LDWURJrQLFR WDPR[LIHQR p JHUDOPHQWH
DGPLQLVWUDGR SRU SHUtRGR TXH QmR GHYH XOWUDSDVVDU DQRV
5DOR[LIHQRp065(PDLVUHFHQWHTXHDSUHVHQWDDWLYLGDGHDJRQLVWDQRUHFHSWRUGHHVWUyJHQRQR
RVVR SRUpP DWLYLGDGH DQWDJRQLVWD HP WHFLGRV PDPiULR H HQGRPHWULDO 6HX PHFDQLVPR GH DomR p
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LPSHGH D SURJUHVVmR GD RVWHRSRURVH HP PXOKHUHV SyVPHQRSiXVLFDV GLVFXWLGD GH PRGR PDLV
2 UDOR[L
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DJHQWHV UHVXOWDUDP HP UHGXomR GH QR GHVHQYROYLPHQWR GH FkQFHU GH PDPD LQYDVLYR 2
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FDVRVGHFkQFHUGHPDPDQmRLQYDVLYRTXHUDOR[LIHQR
FIGURA 29.8 Comparação estrutural de estrógeno (ligante natural) e raloxifeno (MSRE) ligados ao receptor de
estrógeno. O domínio de ligação com o ligante do receptor alfa de estrógeno humano é mostrado em formato de fita, desde o N-
terminal amarelo-amarronzado até o C-terminal azul-escuro. O ligante natural 17β-estradiol (estrógeno) e o modulador seletivo do
receptor de estrógeno (MSRE) raloxifeno são mostrados no formato de preenchedores de espaço. A. Na estrutura ligada ao estrógeno, a
posição da hélice laranja (H12) define a conformação agonista do receptor que recruta coativadores e, assim, regula a transcrição de
genes regulados por estrógeno (ver Figura 29.7). B. Na estrutura ligada ao raloxifeno, a volumosa cadeia lateral do raloxifeno altera a
conformação agonista do receptor (observe que a hélice H12 é substancialmente deslocada). Nessa conformação, o receptor consegue
recrutar alguns coativadores, mas não outros (ver Figura 29.7).
LIHQR p 065(
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I UPDFR DWXD FRPR DQWDJRQLVWD
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)6+ H[yJHQR YHU &DStWXOR R XVR GR FORPLIHQR UDUDPHQWH VH DVVRFLD j VtQGURPH GH
KLSHUHVWLPXODomRRYDULDQD
0XLWRV QRYRV 065( VH HQFRQWUDP HP IDVH ILQDO GH HQVDLRV FOtQLFRV %D]HGR[LIHQR HVWi VHQGR
GHVHQYROYLGRSDUDWUDWDPHQWRGHRVWHRSRURVH2VSHPLIHQRHVWiVHQGRGHVHQYROYLGRSDUDWUDWDPHQWR
GHDWURILDYXOYRYDJLQDOHUHVVHFDPHQWRYDJLQDOHPPXOKHUHVQDPHQRSDXVD
(U[HNVUPZ[HZKVZYLJLW[VYLZKLHUKY}NLUVZ
$QWDJRQLVWDV GRV UHFHSWRUHV GH DQGUyJHQRV LQLEHP FRPSHWLWLYDPHQWH D OLJDomR GH DQGUyJHQRV
HQGyJHQRVDRUHFHSWRUGHDQGUyJHQR3RUHVVHPHFDQLVPRRVDQWDJRQLVWDVGRVUHFHSWRUHVEORTXHLDP
DVDo}HVGHWHVWRVWHURQDHGLKLGURWHVWRVWHURQDVREUHVHXVWHFLGRVDOYR$QWDJRQLVWDVGRVUHFHSWRUHV
GHDQGUyJHQRVLQFOXHPIOXWDPLGDHHVSLURQRODFWRQD)OXWDPLGDIRLDSURYDGDDSHQDVSDUDWUDWDPHQWR
GH FkQFHU GH SUyVWDWD PHWDVWiWLFR SRUpP R IiUPDFR WDPEpP p XWLOL]DGR WHUDSHXWLFDPHQWH QR
WUDWDPHQWR GH KLSHUSODVLD SURVWiWLFD EHQLJQD (VSLURQRODFWRQD RULJLQDOPHQWH DSURYDGD FRPR
DQWDJRQLVWDGRVUHFHSWRUHVGHDOGRVWHURQDYHU&DStWXORWDPEpPDSUHVHQWDDWLYLGDGHDQWDJRQLVWD
VLJQLILFDWLYD QR UHFHSWRU GH DQGUyJHQRV ¬ VHPHOKDQoD GH IOXWDPLGD HVSLURQRODFWRQD SRGH VHU
XWLOL]DGD FRPR LQLELGRU FRPSHWLWLYR GD DomR GD WHVWRVWHURQD 6UWD - IRL WUDWDGD FRP
HVSLURQRODFWRQDSDUDDQWDJRQL]DUDH[FHVVLYDHVWLPXODomRDQGURJrQLFDGHVHXVIROtFXORVSLORVRV
PHOKRUDQGR DVVLP R KLUVXWLVPR 8P FRPSRVWR GHULYDGR GD HVSLURQRODFWRQD GURVSLUHQRQD WHP
HIHLWRV WDQWR SURJHVWDFLRQDLV TXDQWR DQWLDQGURJrQLFRV e XWLOL]DGD FRPR SURJHVWiJHQR HP DOJXQV
FRQWUDFHSWLYRVFRPELQDGRVHVWUyJHQRSURJHVWiJHQR
(U[HNVUPZ[HZKVZYLJLW[VYLZKLWYVNLZ[LYVUH
0LIHSULVWRQD WDPEpP FRQKHFLGD FRPR 58 p DQWDJRQLVWD GRV UHFHSWRUHV GH SURJHVWHURQD
XWLOL]DGDSDUDLQGXomRGHDERUWRDSDUWLUGRGLDGHJUDYLGH]&RQIRUPHDVVLQDODGRSURJHVWHURQDp
GHVXPDLPSRUWkQFLDSDUDDPDQXWHQomRGRHQGRPpWULRGXUDQWHDJUDYLGH]RKRUP{QLRHVWDELOL]DR
UHYHVWLPHQWR XWHULQR H SURPRYH R FUHVFLPHQWR GRV YDVRV H DV DWLYLGDGHV VHFUHWRUDV GD GHFtGXD
0LIHSULVWRQD LQLEH D DomR GD SURJHVWHURQD SRU PHLR GH OLJDomR FRPSHWLWLYD QR UHFHSWRU GH
SURJHVWHURQD2EORTXHLRGDDomRGDSURJHVWHURQDUHVXOWDHPGHWHULRUDomRHPRUWHGDGHFtGXDHD
IDOWD GH QXWULomR SURYHQLHQWH GD GHFtGXD OHYD j PRUWH GR EODVWRFLVWR TXH VH GHVSUHQGH GR ~WHUR
&RPRREODVWRFLVWRQmRHVWiPDLVVHFUHWDQGRK&*RFRUSRO~WHRLQYROXLHHVVDLQYROXomRGHWHUPLQD
UHGXomRHPVtQWHVHHVHFUHomRGHSURJHVWHURQD
0LIHSULVWRQD p FRPXPHQWH DGPLQLVWUDGD HP DVVRFLDomR FRP PLVRSURVWRO DQiORJR GH
SURVWDJODQGLQD YHU &DStWXOR 0LVRSURVWRO HVWLPXOD DV FRQWUDo}HV XWHULQDV H RV HIHLWRV
FRPELQDGRVGRDQWDJRQLVPRGHSURJHVWHURQDHGDVFRQWUDo}HVXWHULQDVVmRPDLVGHHIHWLYRVQR
WpUPLQRGDJUDYLGH]GHSULPHLURWULPHVWUH
&RPR PLIHSULVWRQD p DGPLQLVWUDGD HP GRVH ~QLFD RV HIHLWRV DGYHUVRV UHODFLRQDGRV FRP R
DQWDJRQLVPR GD SURJHVWHURQD VmR UDURV &RP HIHLWR R SULQFLSDO ULVFR GH FRPSOLFDo}HV HVWi
UHODFLRQDGR FRP DERUWR VXEVHTXHQWH TXH SRGH UHVXOWDU HP VDQJUDPHQWR YDJLQDO H[FHVVLYR $OpP
GLVVRDFRDGPLQLVWUDomRGHPLVRSURVWROSRGHFDXVDUQiXVHDVHY{PLWRV
$VRSULVQLO p XP QRYR DQWDJRQLVWD GR UHFHSWRU GH SURJHVWHURQD TXH QmR FDXVD DERUWR PDV TXH
LQLEHRFUHVFLPHQWRGRVWHFLGRVGHULYDGRVGHHQGRPpWULRHPLRPpWULR(VWXGRVSUHOLPLQDUHVLQGLFDP
TXHDVRSULVQLOSRGHVHUHIHWLYRQRWUDWDPHQWRGHHQGRPHWULRVHHOLRPLRPDVXWHULQRVILEURLGHV$V
GLIHUHQoDV QD HVSHFLILFLGDGH WHFLGXDO GH PLIHSULVWRQD H DVRSULVQLO GHYHPVH SURYDYHOPHQWH jV
GLIHUHQoDVHPVXDDomRGHLQIOXHQFLDUDOLJDomRGHFRIDWRUHVGHWUDQVFULomRDRFRPSOH[RGRUHFHSWRU
GHSURJHVWHURQD
/VYTUPVZLHUmSVNVZOVYTVUHPZc*VU[YHJLWsqV
2 GHVHQYROYLPHQWR GH FRQWUDFHSWLYRV VHJXURV H HILFD]HV SDUD PXOKHUHV UHYROXFLRQRX DV SUiWLFDV
VH[XDLV $V GXDV FODVVHV GH FRQWUDFHSWLYRV RUDLV DPSODPHQWH XWLOL]DGDV VmR FRPELQDo}HV GH
HVWUyJHQRSURJHVWiJHQR H FRQWUDFHSomR FRP SURJHVWiJHQR DSHQDV 2 GHVHQYROYLPHQWR GH
FRQWUDFHSomR PDVFXOLQD FRQVWLWXL XPD iUHD DWLYD GH SHVTXLVD H DV DERUGDJHQV DWXDLV SDUD HVVD
WHUDSLDVmRGLVFXWLGDVGHPRGRVXFLQWRQRILQDOGDVHomR
*VU[YHJLW[P]VZJVTIPUHKVZHZZVJPHsLZKLLZ[Y}NLUVWYVNLZ[mNLUV
&RPELQDo}HV GH HVWUyJHQRSURJHVWiJHQR VXSULPHP D VHFUHomR GH *Q5+ /+ H )6+ H R
GHVHQYROYLPHQWR IROLFXODU LQLELQGR D RYXODomR $ FRPELQDomR GH XP HVWUyJHQR H XP
SURJHVWiJHQRFRQVWLWXLRPpWRGRPDLVSRWHQWHFRQKHFLGRGHVXSULPLUDVHFUHomRGH*Q5+/+H
)6+ $ FRDGPLQLVWUDomR GH HVWUyJHQR H SURJHVWiJHQR WDPEpP SRGH LQLELU D JUDYLGH] SRU YiULRV
PHFDQLVPRVVHFXQGiULRVLQFOXLQGRDOWHUDo}HVHPSHULVWDOWLVPRWXEiULRUHFHSWLYLGDGHHQGRPHWULDOH
VHFUHo}HVGHPXFRFHUYLFDO(VVDV~OWLPDVDo}HVMXQWDVSRGHULDPLQLELURWUDQVSRUWHDSURSULDGRGH
yYXOR H HVSHUPDWR]RLGHV PHVPR VH WLYHVVH RFRUULGR RYXODomR (P FRQMXQWR HVVHV PHFDQLVPRV
H[SOLFDPDHILFiFLDGH!GRVFRQWUDFHSWLYRVRUDLVFRPELQDGRV
2V HVWUyJHQRV XWLOL]DGRV QRV FRQWUDFHSWLYRV FRPELQDGRV FRQVLVWHP HP HWLQLOHVWUDGLRO H
PHVWUDQRO)LJXUD2XVRGHHVWUyJHQRV³VHPRSRVLomR´SURPRYHFUHVFLPHQWRHQGRPHWULDOH
HVWXGRVLQLFLDLVGHDQWLFRQFHSFLRQDLVFRPSUHGRPtQLRHVWURJrQLFRHVWDEHOHFHUDPTXHHVVHVDJHQWHV
DXPHQWDP R ULVFR GH FkQFHU HQGRPHWULDO (P GHFRUUrQFLD GHVVH DFKDGR HVWUyJHQR p VHPSUH
DGPLQLVWUDGR FRQFRPLWDQWHPHQWH FRP SURJHVWiJHQR SDUD OLPLWDU D H[WHQVmR GR FUHVFLPHQWR
HQGRPHWULDO
6mRXWLOL]DGRVQXPHURVRVSURJHVWiJHQRV)LJXUDVHQRVFRQWUDFHSWLYRVFRPELQDGRV
H WRGRV VmR SRWHQWHV DJRQLVWDV GRV UHFHSWRUHV GH SURJHVWHURQD 2 SURJHVWiJHQR LGHDO GHYHULD
DSUHVHQWDUDSHQDVDWLYLGDGHQRVUHFHSWRUHVGHSURJHVWHURQDHQWUHWDQWRTXDVHWRGRVRVSURJHVWiJHQRV
DWXDOPHQWH GLVSRQtYHLV WDPEpP H[LEHP DOJXPD UHDWLYLGDGH FUX]DGD DQGURJrQLFD 3URJHVWiJHQRV
YDULDPTXDQWRjVXDDWLYLGDGHDQGURJrQLFD(PEDVHPRODUQRUJHVWUHOHOHYRQRUJHVWUHOVmR RVTXH
DSUHVHQWDPPDLRUDWLYLGDGHDQGURJrQLFDHQTXDQWRQRUHWLQGURQDHDFHWDWRGHQRUHWLQGURQD)LJXUD
DSUHVHQWDPDWLYLGDGHDQGURJrQLFDPDLVEDL[D3URJHVWiJHQRVGHWHUFHLUDJHUDomR±HWLQRGLRO
QRUJHVWLPDWR JHVWRGHQR H GHVRJHVWUHO )LJXUD ± H[LEHP UHDWLYLGDGH FUX]DGD DLQGD PHQRU
FRP UHFHSWRUHV GH DQGUyJHQR 'URVSLUHQRQD p SURJHVWiJHQR VLQWpWLFR TXH WDPEpP H[LEH DWLYLGDGH
DQWLDQGURJrQLFD
&RQWUDFHSWLYRV FRPELQDGRV HVWmR GLVSRQtYHLV HP WUrV VLVWHPDV GH OLEHUDomR DQHO YDJLQDO
DGHVLYRV WUDQVGpUPLFRV H FRPSULPLGRV RUDLV 2 DQHO YDJLQDO FRQVLVWH HP FLOLQGUR GH VLOLFRQH
FRQWHQGRHWLQLOHVWUDGLROHSURJHVWiJHQRRHWRQRJHVWUHO2VHVWHURLGHVVmROLEHUDGRVFRPFLQpWLFDGH
RUGHP]HURYHU&DStWXOR2DQHOpDSOLFDGRQDYDJLQDRQGHSHUPDQHFHSRUGLDV(PVHJXLGD
pUHPRYLGRHGLDVGHSRLVFRORFDVHQRYRDQHO'XUDQWHRVGLDVDSyVDUHPRomRGRDQHOYDJLQDO
SRGH RFRUUHU PHQVWUXDomR YHU DGLDQWH 2 DQWLFRQFHSFLRQDO WUDQVGpUPLFR FRQVLVWH HP PDWUL] TXH
OLEHUDFRQWLQXDPHQWHHWLQLOHVWUDGLROHSURJHVWiJHQRVLQWpWLFRDQRUHOJHVWURPLQD2DGHVLYRpWURFDGR
VHPDQDOPHQWH GXUDQWH VHPDQDV 1D TXDUWD VHPDQD R DGHVLYR QmR p XWLOL]DGR H SRGH RFRUUHU
PHQVWUXDomR
2V HVTXHPDV FOiVVLFRV GH DQWLFRQFHSFLRQDLV RUDLV FRPELQDGRV FRQVLVWHP QD DGPLQLVWUDomR GH
FRPSULPLGRVGXUDQWHGLDVVHJXLGRVGHGLDVGHStOXODSODFHER2SHUtRGRGHGLDVFRP
SODFHERUHPRYHDHVWLPXODomRKRUPRQDOH[yJHQDSURPRYHQGRDGHVFDPDomRGRHQGRPpWULRH
FRQVHTXHQWH VDQJUDPHQWR &RPR D DGPLQLVWUDomR GH SURJHVWiJHQR GXUDQWH WRGR R FLFOR LQLEH R
FUHVFLPHQWR SUROLIHUDWLYR GR HQGRPpWULR D PDLRULD GDV PXOKHUHV WHP SHUtRGRV PHQVWUXDLV PHQRV
LQWHQVRV TXDQGR ID]HP XVR GH DQWLFRQFHSFLRQDLV RUDLV FRPELQDGRV H FRP IUHTXrQFLD R FLFOR
PHQVWUXDOWRUQDVHPDLVUHJXODU$IRUPXODomRGRFLFORWHYHSRUREMHWLYRVLPXODUXPFLFORGH
GLDVWRGDYLDpUHODWLYDPHQWHDUELWUiULR([LVWHWDPEpPDSRVVLELOLGDGHGHFRPELQDUHPEDODJHQVGH
StOXODVREWHQGR³FLFORVORQJRV´GHStOXODVDWLYDVGLDVVHJXLGDVSRUGLDVVHPKRUP{QLRRX
GLDVGHStOXODVKRUPRQDLVDWLYDV VHJXLGRVSRUGLDVVHPKRUP{QLR2VHVTXHPDVFRP³FLFORV
ORQJRV´ UHGX]HP D IUHTXrQFLD GR VDQJUDPHQWR PHQVWUXDO PDV DXPHQWDP D IUHTXrQFLD GR FKDPDGR
VDQJUDPHQWR GH HVFDSH e SRVVtYHO LQVWLWXLU FLFOR DLQGD PDLV ORQJR FRP HWLQLOHVWUDGLRO H
OHYRQRUJHVWUHOQRTXDODDVVRFLDomRpDGPLQLVWUDGDGXUDQWHGLDVHVHJXLGDSRUGLDVGHSODFHER
(VVDIRUPXODomRTXHDSUHVHQWDHILFiFLDFRQWUDFHSWLYDLJXDOjGRHVTXHPDFOiVVLFRUHGX]SDUDR
Q~PHURWRWDOGHFLFORVPHQVWUXDLVSRUDQR'LVS}HVHWDPEpPGHIRUPXODo}HVTXHFRQWrPStOXODV
GHKRUP{QLRVGLiULRVFRPGLDVGHSODFHER8PDYDQWDJHPGHVVDIRUPXODomRpTXHDRYXODomRQmR
WHQGHDRFRUUHUVHDPXOKHUVHHVTXHFHUGHLQLFLDUVHXQRYRFLFORGHStOXODVSRURXGLDV
FIGURA 29.9 Estrutura dos estrógenos sintéticos. Etinilestradiol e mestranol são usados em contraceptivos combinados
(estrógeno e progestágeno).
FIGURA 29.10 Estrutura dos progestágenos sintéticos. Acetato de medroxiprogesterona é comumente associado a estrógeno
para terapia hormonal em mulheres pós-menopáusicas. Com frequência, acetato de megestrol é utilizado como terapia para câncer
endometrial. Noretindrona foi o primeiro progestágeno a ser sintetizado em quantidades suficientes para produção em massa de
contraceptivos combinados de estrógeno-progestágeno. Acetato de noretindrona é comumente utilizado em contraceptivos; é
metabolizado ao composto original, noretindrona.
$VIRUPXODo}HVGHDQWLFRQFHSFLRQDLVRUDLVFRPELQDGRVLQFOXHPHVTXHPDVKRUPRQDLVPRQRIiVLFR
H WULIiVLFR $ IRUPXODomR SDGUmR XWLOL]DGD SHOD PDLRULD GDV PXOKHUHV FRQVLVWH HP GRVH FRQVWDQWH
PRQRIiVLFD GH HVWUyJHQR H SURJHVWiJHQR GXUDQWH GLDV $V SUHSDUDo}HV WULIiVLFDV LQFRUSRUDP
GRVHFRQVWDQWHGHHVWUyJHQRFRPGRVHGHSURJHVWiJHQRTXHDXPHQWDDFDGDVHPDQDGXUDQWHRVGLDV
GR FLFOR $ SULQFLSDO YDQWDJHP GD DGPLQLVWUDomR WULIiVLFD p TXH D TXDQWLGDGH WRWDO GH
SURJHVWiJHQR DGPLQLVWUDGD D FDGD PrV p UHGX]LGD &RP HIHLWR D WHQGrQFLD JHUDO QHVVHV ~OWLPRV
DQRVWHPVLGRGLPLQXLUDVTXDQWLGDGHVGHHVWUyJHQRHSURJHVWiJHQRDRPHQRUQtYHOQHFHVViULRSDUD
LQLELU D RYXODomR (QWUHWDQWR QmR H[LVWH QHQKXPD GLIHUHQoD FODUDPHQWH HVWDEHOHFLGD HP HIHLWRV
DGYHUVRV RX HILFiFLD FOtQLFD GD WHUDSLD PRQRIiVLFD HP FRPSDUDomR FRP D WULIiVLFD (P JHUDO
SUHIHUHVHDPHQRUGRVHHIHWLYDGHHWLQLOHVWUDGLROXPDYH]TXHVHDFUHGLWDTXHRHVWUyJHQRHPEDL[D
GRVHWHPDFDSDFLGDGHGHUHGX]LURULVFRGHWURPERVHYHQRVDSURIXQGDYHUDGLDQWH
9iULRV HVWXGRV IRUDP FRQGX]LGRV SDUD DYDOLDU RV HIHLWRV DGYHUVRV GR XVR SURORQJDGR GH
FRQWUDFHSWLYRV(VVHVHVWXGRVPRVWUDUDPTXHDLQFLGrQFLDGHWURPERVHYHQRVDSURIXQGDHHPEROLD
SXOPRQDUDXPHQWDFRPDFRQWUDFHSomRRUDOFRPELQDGD(VVDVFRPSOLFDo}HVRFRUUHPUDUDPHQWHHR
Q~PHURDEVROXWRGHHYHQWRVDGYHUVRVpEDL[ReLQWHUHVVDQWHPHQFLRQDUTXHJUDYLGH]HVWiDVVRFLDGD
DULVFRPDLRUGHWURPERVHYHQRVDSURIXQGDHHPEROLDSXOPRQDUTXHRWUDWDPHQWRFRPFRQWUDFHSWLYRV
RUDLVFRPELQDGRV(VWXGRVQmRFRQVHJXLUDPGHPRQVWUDUQHQKXPDXPHQWRRXUHGXomRQDLQFLGrQFLD
GHFkQFHUGHPDPD2XVRGRVDQWLFRQFHSFLRQDLVRUDLVVHDVVRFLDDDXPHQWRQDLQFLGrQFLDGHGRHQoD
GD YHVtFXOD ELOLDU YLVWR TXH HVWUyJHQRV DXPHQWDP D FRQFHQWUDomR ELOLDU GH FROHVWHURO HP UHODomR
FRPDGRVVDLVELOLDUHVHDFRQVHTXHQWHUHGXomRQDVROXELOLGDGHGRFROHVWHUROSURPRYHDIRUPDomR
GH FiOFXORV YHVLFXODUHV $QWLFRQFHSFLRQDLV RUDLV QmR GHYHP VHU DGPLQLVWUDGRV D PXOKHUHV FRP
PDLV GH DQRV GH LGDGH TXH IXPDP YLVWR TXH D DGPLQLVWUDomR GH FRQWUDFHSWLYRV D HVVD
SRSXODomRHVWiDVVRFLDGDDDXPHQWRQDLQFLGrQFLDGHHYHQWRVFDUGLRYDVFXODUHVWURPEyWLFRV
(VWXGRV UHFHQWHV VH FRQFHQWUDUDP PDLV QRV EHQHItFLRV TXH QRV HIHLWRV DGYHUVRV GRV
DQWLFRQFHSFLRQDLV RUDLV 2V PRGHUQRV DQWLFRQFHSFLRQDLV RUDLV FRPELQDGRV UHGX]HP R ULVFR GH
FkQFHUHQGRPHWULDOSURYDYHOPHQWHSHORIDWRGHDDGPLQLVWUDomRFRQFRPLWDQWHGHSURJHVWiJHQRLQLELU
R FUHVFLPHQWR HQGRPHWULDO $OpP GLVVR D DGPLQLVWUDomR H[yJHQD GH XPD DVVRFLDomR GH
HVWUyJHQRSURJHVWiJHQR GLPLQXL R ULVFR GH FkQFHU RYDULDQR SURYDYHOPHQWH DR UHGX]LU RV QtYHLV
FLUFXODQWHV GH JRQDGRWURILQDV 'H PRGR JOREDO R FRQVHQVR p GH TXH DQWLFRQFHSFLRQDLV RUDLV
DSUHVHQWDPPDLVHIHLWRVFOtQLFRVEHQpILFRVTXHSUHMXGLFLDLV
FIGURA 29.11 Estrutura de progestágenos comumente utilizados em contraceptivos orais. Levonorgestrel é o mais
androgênico dos progestágenos mais comumente utilizados. Gestodeno, norgestimato e desogestrel são menos androgênicos que
levonorgestrel.
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GH SURJHVWiJHQRV RUDLV HP EDL[DV GRVHV 1RV (8$ RV GRLV DQWLFRQFHSFLRQDLV RUDLV Vy FRP
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VHIRUDGPLQLVWUDGRGHQWURGHKDSyVDH[SRVLomR/HYRQRUJHVWUHOpSRWHQWHSURJHVWiJHQRFDSD]
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HPSUHJDUDWHUDSLDKRUPRQDODSHQDVSDUDWUDWDPHQWRGHVLQWRPDVLQF{PRGRVFRPRRVYDVRPRWRUHV
RXUHVVHFDPHQWRYDJLQDOEHPFRPRHPXWLOL]DUDPHQRUGRVHSRVVtYHOGHWHUDSLDKRUPRQDOGXUDQWHR
PDLV FXUWR SHUtRGR $SyV D SXEOLFDomR GRV UHVXOWDGRV GR HVWXGR :+, HP KRXYH UHGXomR
DFHQWXDGDGRQ~PHURGHPXOKHUHVQDPHQRSDXVDTXHUHFHEHUDPWHUDSLDGHUHSRVLomRFRPHVWUyJHQR
SURJHVWiJHQRHTXHGDSDUDOHODGRQ~PHURGHFDVRVGHFkQFHUGHPDPDGLDJQRVWLFDGRV
TABELA 29.3 Resumo dos achados do Women’s Health Initiative (WHI).
Os dados representam as relações de risco (intervalos de confiança de 95%) de vários eventos durante tratamento com terapia hormonal ou placebo. Os intervalos de confiança que
cruzam o valor de 1,00 não são estatisticamente significativos (p > 0,05).
+i PXLWRV SURJHVWiJHQRV VLQWpWLFRV GLVSRQtYHLV SDUD XVR QD WHUDSLD KRUPRQDO GH PXOKHUHV QD
PHQRSDXVD(VWXGRVHSLGHPLROyJLFRVUHFHQWHVGHVFUHYHPTXHSURJHVWHURQDPLFURQL]DGDVHDVVRFLDD
PHQRU ULVFR GH FkQFHU GH PDPD TXH RXWURV SURJHVWiJHQRV VLQWpWLFRV FRPXPHQWH SUHVFULWRV FRPR
DFHWDWRGHPHGUR[LSURJHVWHURQD$PLFURQL]DomRpXPSURFHVVRQRTXDORVFULVWDLVGHSURJHVWHURQD
VmRVLQWHWL]DGRVFRPGLkPHWURQDIDL[DGHQDQ{PHWURVIDFLOLWDQGRVXDDEVRUomRSRUYLDRUDO
$ H[HPSOR GRV FRQWUDFHSWLYRV D WHUDSLD KRUPRQDO HVWi GLVSRQtYHO QD IRUPD GH FRPSULPLGRV
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WUDQVGpUPLFRV GH WHVWRVWHURQD HVVH VLVWHPD GH OLEHUDomR GR IiUPDFR WHP DV YDQWDJHQV GH WRUQDU
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GHSULPHLUDSDVVDJHP7HVWRVWHURQDWDPEpPHVWiGLVSRQtYHOHPIRUPXODomRGHJHOWySLFRFRPRXVR
GHVVD SUHSDUDomR HP HVTXHPD GH DSOLFDomR YH]GLD RV QtYHLV SODVPiWLFRV GH WHVWRVWHURQD
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Gonadorrelina
Gosserrelina
Leuprolida
Nafarrelina
Cetrorrelix
Ver Resumo farmacológico: Capítulo 26
Ganirrelix
Mecanismo – Inibem a 5α-redutase, enzima que converte testosterona em di-hidrotestosterona em próstata, fígado e pele. Finasterida é inibidor seletivo de 5α-redutase de tipo II,
enquanto dutasterida inibe 5α-redutases de tipos I e II
Inibidores da aromatase
Mecanismo – Anastrozol e letrozol são inibidores competitivos da aromatase, enzima que catalisa a formação de estrógenos a partir de precursores androgênicos. Exemestano e
formestano são inibidores irreversíveis (covalentes) da aromatase
Mecanismo – Antagonista do estrógeno em alguns tecidos e agonista do estrógeno em outros tecidos. A base da seletividade tecidual pode estar relacionada com a expressão tecidual
específica de subtipos de receptores de estrógeno e à capacidade diferencial do complexo ligante-receptor de recrutar coativadores e correpressores da transcrição
História de trombose
venosa profunda ou
embolia pulmonar
quando utilizado Antagonista do receptor de estrógeno no tecido
para prevenção do mamário e agonista parcial em endométrio e osso
Prevenção de câncer de mama
Neoplasia maligna do câncer de mama ou
endométrio, acidente vascular carcinoma ductal in Como o tamoxifeno estimula o crescimento
Tratamento paliativo de câncer
cerebral, catarata, embolia situ; em pacientes endometrial, sua administração associa-se a
de mama metastático
Tamoxifeno pulmonar com câncer de mama aumento de quatro a seis vezes na incidência de
invasivo, os câncer endometrial
Terapia adjuvante de câncer de
Ondas de calor, menstruação benefícios de
mama após excisão primária do
anormal, secreção vaginal tamoxifeno superam Habitualmente administrado por período não
tumor (nodulectomia)
os riscos de doença maior que 5 anos, a fim de minimizar o risco de
tromboembólica câncer endometrial iatrogênico
recorrente
Gravidez
Gravidez
Antagonista do receptor de estrógeno em
Disfunção não hipotálamo e adeno-hipófise e agonista parcial
controlada de nos ovários; desinibe a liberação de GnRH,
Tromboembolia tireoide ou adrenal resultando em níveis elevados de LH e FSH; o
Infertilidade feminina, aumento do FSH estimula o crescimento folicular,
Cistos ovarianos, hipertrofia Doença hepática
Clomifeno decorrente de distúrbio resultando em sinal deflagrador estrogênico,
ovariana, rubor, sintomas
ovulatório surto de LH e ovulação
vasomotores, desconforto Carcinoma endometrial
abdominal
Ao contrário do FSH exógeno, o uso do clomifeno
Cistos ovarianos
raramente está associado à síndrome de
Lesão intracraniana hiperestimulação ovariana
orgânica
Bazedoxifeno (em
Osteoporose Em estudos clínicos
investigação)
Mecanismo – Inibem competitivamente a ligação do estrógeno ao receptor, bloqueando a ação do estrógeno nos tecidos-alvo
Mecanismo – Inibem competitivamente a ligação de di-hidrotestosterona e testosterona ao receptor, bloqueando suas ações nos tecidos-alvo
Mecanismo – Inibem a ligação de progesterona ao receptor; as diferenças na especificidade tecidual de mifepristona e asoprisnil devem-se, provavelmente, às suas diferenças na
influência da ligação de coativadores e correpressores da transcrição ao complexo do receptor de progesterona
Mecanismo – Supressão da secreção de GnRH, LH e FSH e do desenvolvimento folicular, com consequente inibição da ovulação; mecanismos secundários da prevenção da gravidez incluem
alterações em peristaltismo da tuba uterina, receptividade do endométrio e secreções mucosas cervicais, que, em seu conjunto, impedem o transporte apropriado do ovo e dos
espermatozoides
Câncer de mama
Como o estrógeno sem oposição aumenta o risco de
Câncer endometrial ou câncer endometrial, o estrógeno é sempre
outras neoplasias coadministrado com progestágeno em mulheres
dependentes de com útero
Estrógenos:
estrógeno
Progestágenos variam em sua atividade
Etinilestradiol
Doença vascular androgênica
Mestranol cerebral ou
coronariopatia Norgestrel e levonorgestrel são os que apresentam
Progestágenos: maior atividade androgênica; noretindrona e
Tromboembolia arterial e venosa,
Icterícia colestática da acetato de noretindrona exibem atividade
embolia pulmonar, trombose
Norgestrel gravidez ou icterícia androgênica média; etinodiol, norgestimato,
cerebral, doença da vesícula
com uso prévio de gestodeno e desogestrel apresentam baixa
biliar, hipertensão, neoplasia
Levonorgestrel contraceptivos reatividade cruzada com receptores de estrógeno;
hepática
hormonais drospirenona é progestágeno sintético que
Noretindrona Contracepção também apresenta atividade antiandrogênica
Menstruação anormal,
sangramento inesperado, Tumores hepáticos
Acetato de noretindrona benignos ou Contraceptivos com associações de estrógeno-
hipersensibilidade das
malignos progestágeno estão disponíveis em comprimidos
Etinodiol mamas, sintomas de
orais, anel vaginal e adesivos transdérmicos
distensão, enxaqueca,
Hipertensão grave
Norgestimato alteração do peso
Formulações orais bifásicas ou trifásicas apresentam
Imobilização menores quantidades totais de progestágeno a
Gestodeno
prolongada cada mês
Desogestrel Gravidez Prefere-se a dose efetiva mais baixa de
etinilestradiol para reduzir o risco de trombose
Drospirenona Mulheres fumantes venosa profunda
com mais de 35 anos
de idade Levonorgestrel também é utilizado para
contracepção de emergência (do dia seguinte)
Distúrbios trombóticos
Mecanismo – Alteram a frequência dos pulsos de GnRH e diminuem a responsividade da adeno-hipófise ao GnRH. Mecanismos secundários de prevenção da gravidez incluem alterações
em peristaltismo da tuba uterina, receptividade do endométrio e secreções mucosas cervicais que, em seu conjunto, impedem o transporte apropriado do ovo e dos espermatozoides
Mecanismo – Reposição de testosterona para produzir efeitos androgênicos, incluindo crescimento e maturação da próstata, das glândulas seminais, do pênis e do escroto;
desenvolvimento da distribuição masculina dos pelos; aumento da laringe; espessamento das cordas vocais; e alterações em musculatura e distribuição da gordura do corpo