Formation, Function, and Persistence of the Corpora Lutea of the African Elephant (Loxodonta africana)

1975 ◽  
Vol 56 (1) ◽  
pp. 30-43 ◽  
Author(s):  
N. S. Smith ◽  
I. O. Buss
2006 ◽  
Vol 361 (1469) ◽  
pp. 821-834 ◽  
Author(s):  
W.R Allen

The African elephant reproduces so efficiently in the wild that overpopulation is now a serious problem in some game parks in Zimbabwe, Botswana and South Africa. The female reaches puberty between 10 and 12 years of age in the wild and, when in captivity, shows oestrous cycles of 14–15 weeks duration. She readily conceives a singleton in the wild yet her uterus has the capacity for twins. She shows a gestation length of 22 months and, in the wild, shows a population density and feed dependent intercalving interval of 4–8 years. The trophoblast erodes the lumenal epithelium of the endometrium and stimulates upgrowths of blood vessel-containing stromal villi, which develop eventually into the broad, tightly folded lamellae of the zonary, endotheliochorial placenta. Significant quantities of leaked maternal erythrocytes and ferric iron are phagocytosed by specialized trophoblast cells in the haemophagous zones at the lateral edges of the placental band. Although the placenta itself is endocrinologically inert, the foetal gonads, which enlarge greatly during the second half of pregnancy can synthesize 5α-dihydryoprogesterone and other 5α pregnane derivatives from cholesterol and pregnenolone. These products may synergize with progestagens secreted by the 2–8 large corpora lutea which are always present in the maternal ovaries throughout gestation to maintain the pregnancy state.


2017 ◽  
Vol 52 (6) ◽  
pp. 1138-1141 ◽  
Author(s):  
Y Yamamoto ◽  
K Nagaoka ◽  
Y Kamite ◽  
G Watanabe ◽  
T Allen ◽  
...  

Reproduction ◽  
1969 ◽  
Vol 20 (1) ◽  
pp. 111-117 ◽  
Author(s):  
J. G. SMITH ◽  
J. HANKS ◽  
R. V. SHORT

Reproduction ◽  
2012 ◽  
Vol 143 (6) ◽  
pp. 845-854 ◽  
Author(s):  
F J Stansfield ◽  
W R Allen

The ovaries of eight African elephant foetuses and their mothers between 2 and 22 months of gestation, and those of two cycling and two lactating elephants, were examined grossly, histologically and immunocytochemically, with emphasis on the development and regression of accessory corpora lutea (CL) of pregnancy and the steroidogenic capacities of the accessory CL and the foetal ovaries. The results supported recent findings that the accessory CL form as a result of luteinisation, with and without ovulation, of medium-sized follicles during the 3-week inter-luteal period of the oestrous cycle. They enlarge significantly and become steroidogenically active around 5 weeks of gestation, probably in response to the placental lactogen which is secreted by the implanting trophoblast of the conceptus. The large luteal cells stained strongly for 3β hydroxysteroid dehydrogenase (3βHSD) activity throughout the 22-month gestation period although they showed vacuolation and other degenerative changes in the final months of gestation coincident with hypertrophy and hyperplasia of 3βHSD-positive interstitial cells in the foetal gonads. It is proposed that the progestagens secreted by the enlarged gonads of the elephant foetus may function both to assist the maternal ovaries in supporting the pregnancy state and to induce torpor and intrauterine immobility of the rapidly growing foetus.


Reproduction ◽  
2005 ◽  
Vol 130 (5) ◽  
pp. 713-720 ◽  
Author(s):  
W R Allen ◽  
S Mathias ◽  
M Ford

The gonads, both ovaries and testes, of 44 elephant fetuses weighing 0.09–112 kg (6.1–21.3 months gestation) were examined grossly and histologically. As in equids, elephant fetal gonads undergo a phase of marked growth and enlargement during the second half of gestation, which is more pronounced in ovaries than testes due to growth and antrum formation of numerous follicles in the former. Stromal cells undergo hypertrophy and transformation to form zones of interstitial cells that are associated with the enlarged follicles in the ovaries and in which the primitive seminiferous tubules are embedded in the testes. The interstitial cells have the capacity to synthesize 5α-dihydroprogesterone and other 5α-reduced progestagens from cholesterol and pregnenelone and the hypothesis is raised that these fetal gonadal progestagens may supplement significantly the progestagens secreted by the multiple large corpora lutea of pregnancy in the elephant.


2007 ◽  
Vol 269 (1) ◽  
pp. 118-127 ◽  
Author(s):  
Gunter F. Egger ◽  
Kirsti Witter ◽  
Gerald Weissengruber ◽  
Gerhard Forstenpointner

Bothalia ◽  
2018 ◽  
Vol 48 (1) ◽  
Author(s):  
Judith T. Webber ◽  
Michelle D. Henley ◽  
Yolanda Pretorius ◽  
Michael J. Somers ◽  
Andre Ganswindt

Background: Faecal hormone metabolite measurement is a widely used tool for monitoring reproductive function and response to stressors in wildlife. Despite many advantages of this technique, the delay between defaecation, sample collection and processing may influence steroid concentrations, as faecal bacterial enzymes can alter steroid composition post-defaecation.Objectives: This study investigated changes in faecal glucocorticoid (fGCM), androgen (fAM) and progestagen (fPM) metabolite concentrations in faeces of a male and female African elephant (Loxodonta africana) post-defaecation and the influence of different faeces-drying regimes.Method: Subsamples of fresh faeces were frozen after being dried in direct sun or shade for 6, 20, 24, 48 and 72 h and 7 and 34 days. A subset of samples for each sex was immediately frozen as controls. Faecal hormone metabolite concentrations were determined using enzyme immunoassays established for fGCM, fAM and fPM monitoring in male and female African elephants.Results: Hormone metabolite concentrations of all three steroid classes were stable at first, but changed distinctively after 20 h post-defaecation, with fGCM concentrations decreasing over time and fPM and fAM concentrations steadily increasing. In freeze-dried faeces fGCM concentrations were significantly higher than respective concentrations in sun-dried material, which were in turn significantly higher than fGCM concentrations in shade-dried material. In contrast, fAM concentrations were significantly higher in sun- and shade-dried faeces compared to freeze-dried faeces. Higher fPM concentrations were also found in air-dried samples compared to lyophilised faeces, but the effect was only significant for sun-dried material.Conclusion: The revealed time restriction for collecting faecal material for hormone monitoring from elephants in the wild should be taken into account to assure reliable and comparable results. However, if logistics allow a timely collection, non-invasive hormone measurement remains a powerful and reliable approach to provide information about an elephant’s endocrine status.


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