| Preface |
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xi | |
| Acknowledgements |
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xiv | |
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xviii | |
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Mammalian ovaries, Graafian follicles and oocytes: selected historical landmarks |
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1 | (23) |
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1 | (1) |
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Steps in classical antiquity |
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1 | (2) |
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Sixteenth and seventeenth century contributions |
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3 | (11) |
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Eighteenth and nineteenth century views |
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14 | (2) |
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Twentieth century highlights |
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16 | (3) |
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Prospects for the current century |
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19 | (1) |
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20 | (4) |
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Formation and structure of ovaries: elaboration of follicular compartments |
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24 | (36) |
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24 | (1) |
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24 | (3) |
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Differentiation of an ovary; primordial germ cells |
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27 | (6) |
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Oogenesis, meiosis, growth of oocyte |
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33 | (5) |
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Formation and function of zona pellucida |
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38 | (4) |
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Follicular growth and formation of a Graafian follicle |
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42 | (6) |
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Follicular development, acquisition of follicle stimulating hormone dependence |
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48 | (2) |
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Transcription factors in folliculogenesis |
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50 | (1) |
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Oocyte macromolecules and maternal RNA programme |
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51 | (1) |
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51 | (1) |
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52 | (8) |
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Physiology of the ovaries and maturing Graafian follicles |
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60 | (46) |
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60 | (1) |
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61 | (8) |
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Ovarian and neighbouring lymphatic pathways |
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69 | (8) |
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Ovarian innervation, especially of follicles |
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77 | (6) |
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83 | (7) |
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Temperature gradients within the ovaries |
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90 | (6) |
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Why do Graafian follicles grow so large? |
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96 | (2) |
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98 | (1) |
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99 | (7) |
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Ovarian follicular-antral fluid |
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106 | (32) |
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106 | (1) |
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Formation of follicular fluid |
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107 | (3) |
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Physical condition of follicular fluid |
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110 | (2) |
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Composition of follicular fluid |
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112 | (10) |
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Intra-follicular pressure, PO2, PCO2, pH |
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122 | (2) |
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Contribution to Fallopian tube and peritoneal fluids |
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124 | (3) |
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Involvement of follicular fluid in events of fertilisation |
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127 | (3) |
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130 | (1) |
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131 | (7) |
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Endocrine potential and function of a Graafian follicle |
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138 | (48) |
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138 | (1) |
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Steroids and gonadotrophins: `two-cell' theory of oestradiol synthesis |
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139 | (8) |
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Steroid acute regulatory protein |
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147 | (3) |
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Ovarian proteins - inhibin, activin and follistatin |
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150 | (8) |
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158 | (5) |
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Cytokines and eicosanoids |
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163 | (6) |
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Endorphins and enkephalins |
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169 | (1) |
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Involvement of nitric oxide |
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170 | (2) |
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172 | (1) |
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172 | (14) |
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Follicular recruitment, growth and development: selection - or atresia |
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186 | (38) |
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186 | (1) |
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Recruitment of follicles, selection, dominance |
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187 | (1) |
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Waves of follicular development |
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188 | (9) |
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Endocrine activity associated with dominance |
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197 | (1) |
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Models for follicular selection and dominance |
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198 | (6) |
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Follicle growth inhibitory factors |
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204 | (1) |
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Atresia of follicles and germ cells |
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204 | (5) |
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Apoptosis within ovarian follicles |
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209 | (6) |
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215 | (1) |
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216 | (8) |
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Follicular responses to the pre-ovulatory surge of gonadotrophic hormones |
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224 | (38) |
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224 | (2) |
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Events underlying the pre-ovulatory surge |
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226 | (3) |
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Gonadotrophin surge attenuating factor |
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229 | (1) |
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230 | (14) |
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Expansion and mucification of cumulus oophorus |
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244 | (4) |
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Extracellular matrix of follicle |
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248 | (2) |
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Remodelling of basement membrane |
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250 | (1) |
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251 | (1) |
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252 | (10) |
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The process of ovulation and shedding of an oocyte |
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262 | (33) |
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262 | (1) |
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Spontaneous versus induced ovulation |
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263 | (3) |
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Timing of ovulation and dimensions of follicle |
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266 | (2) |
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Process of ovulation - general features |
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268 | (2) |
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Process of ovulation - morphological highlights |
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270 | (4) |
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Process of ovulation - biochemical events |
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274 | (2) |
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Contribution of leucocytes and cytokines |
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276 | (5) |
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Role of fimbriated extremity of Fallopian tube |
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281 | (1) |
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Ischaemic model for studying ovulation |
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282 | (1) |
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Genes involved in the ovulatory cascade |
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283 | (1) |
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284 | (2) |
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286 | (9) |
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Post-ovulatory fate of follicle and oocyte: contributions of somatic cells and follicular fluid |
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295 | (30) |
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295 | (1) |
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Collapsed follicle evolves into corpus luteum |
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296 | (1) |
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Role of fimbriated infundibulum, cilia and myosalpinx |
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297 | (4) |
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Liberated follicular cells as paracrine tissue |
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301 | (3) |
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Contribution and fate of follicular fluid |
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304 | (2) |
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Regional fluid environments within the Fallopian tube(s) |
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306 | (1) |
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Local ovarian influences on tubal physiology |
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307 | (3) |
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Increasing progesterone secretion modifies tubal physiology |
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310 | (1) |
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Progression of fertilised versus unfertilised eggs |
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311 | (2) |
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Post-ovulatory ageing of oocytes |
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313 | (3) |
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316 | (1) |
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317 | (8) |
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Failure of ovulation: status of the gonads |
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325 | (20) |
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325 | (1) |
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Cystic follicles in animals |
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326 | (2) |
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Polycystic ovarian disease in women |
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328 | (3) |
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331 | (2) |
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333 | (1) |
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Ovotestis and ovulation failure |
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334 | (2) |
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Ovulation failure as a response to stress |
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336 | (1) |
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Leptin involvement in ovulation failure |
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337 | (1) |
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338 | (1) |
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339 | (6) |
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Induction of ovulation in women and domestic animals |
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345 | (21) |
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345 | (1) |
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Treatments for overcoming anovulation in women |
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346 | (4) |
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Induction of multiple ovulation in women |
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350 | (5) |
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Maintenance of a functional corpus luteum |
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355 | (1) |
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Control of ovulation time in animals |
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356 | (1) |
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Induction of superovulation in animals |
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357 | (3) |
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Manipulation of prepuberal animals |
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360 | (1) |
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361 | (1) |
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362 | (4) |
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Concluding thoughts and a current perspective |
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366 | (13) |
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366 | (1) |
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366 | (2) |
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Formation of ovarian follicles |
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368 | (1) |
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Blood vessels, lymphatics, innervation and temperature |
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369 | (1) |
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Contribution of antral fluid |
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370 | (1) |
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Endocrine potential of Graafian follicle |
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371 | (1) |
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Follicular selection, dominance, atresia |
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372 | (1) |
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Responses to the gonadotrophin surge |
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373 | (1) |
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Components of ovulation and shedding of the oocyte |
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374 | (1) |
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Post-ovulatory fate of follicle and contents |
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375 | (1) |
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Ovulatory failure and ovarian anomalies |
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376 | (1) |
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Induction of ovulation and control of ovulation time |
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377 | (2) |
| Index |
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379 | |