THE PROBLEM OF SPECIFICITY IN SEROLOGIC DETERMINATION OF HUMAN CHORIONIC GONADOTROPHIN

1963 ◽  
Vol 42 (4) ◽  
pp. 485-497 ◽  
Author(s):  
Sam Brody ◽  
Gun Carlström

ABSTRACT Rabbit antisera, prepared against a commercial, highly purified preparation of human chorionic gonadotrophin, have been examined with regard to their serologic specificity. Analyses were carried out using procedures of immunodiffusion and complement fixation. Heterogeneity of the immune system is confirmed, and the distribution and serological relationship of unspecific antigens in urine and serum examined. The effect of various methods on the elimination of unspecific antibodies is shown. The implications of these findings on the immunoassay of human chorionic gonadotrophin in body fluids are discussed.

1975 ◽  
Vol 65 (1) ◽  
pp. 73-82 ◽  
Author(s):  
A. K. GOFF ◽  
PATRICIA W. MAJOR

SUMMARY Concentrations of cyclic AMP were measured in rabbit ovaries at various times after injection of an ovulatory dose of human chorionic gonadotrophin (HCG). A biphasic increase in cyclic AMP concentration occurred during the preovulatory period, with peaks 30 min and 3–4 h after HCG injection. Concentrations of cyclic AMP had returned to those observed in ovaries of control oestrous animals before the onset of ovulation 10–12 h after administration of HCG, and remained low throughout the period of pseudopregnancy. Concentrations of cyclic AMP in the newly formed and developing corpora lutea were similar to the concentrations observed in the remainder of the tissue during this period. No significant increase in cyclic AMP concentration was observed 7–9 days after initiation of ovulation. Concentrations of ATP were also investigated during the preovulatory period. The dose– response relationship of HCG to cyclic AMP production in oestrous rabbit ovaries was investigated.


1962 ◽  
Vol 39 (4) ◽  
pp. 539-546 ◽  
Author(s):  
Leif Wide ◽  
Carl Gemzell

ABSTRACT An immunological method to assay human pituitary luteinizing hormone (HPLH) in urine is described. It is based on the fact that HPLH crossreacts with human chorionic gonadotrophin (HCG) in an haemagglutination inhibition reaction between HCG-coated blood cells and rabbit HCG-antisera. During the menstrual cycle the excretion of HPLH reached a peak of 200–400 U per liter at the time of ovulation. In the urine of post-menopausal women the concentration of HPLH was between 100 and 400 U per liter. In the urine of adult men the concentration of HPLH was between 50 and 160 U per liter.


1968 ◽  
Vol 59 (1) ◽  
pp. 105-119 ◽  
Author(s):  
B. C. Goverde ◽  
F. J. N. Veenkamp ◽  
J. D. H. Homan

ABSTRACT Six preparations of Human Chorionic Gonadotrophin (HCG), differing in purity and biological potency, were analysed for their carbohydrate and amino acid composition. The results of the determinations indicated a certain relation between the biological potency on the one hand, and the content of certain substances, particularly sialic acid and fucose (both carbohydrate terminal groups of glycoproteins), on the other. As the sialic acid fraction contained only N-acetyl-neuraminic acid (NANA), a true quantitative determination could be made. Two methods used for the release of NANA were compared and it was found that neuraminidase from Vibrio cholerae released 96% of the amount of NANA which could be released by 0.01 n hydrochloric acid hydrolysis. Based on the results of biological and NANA assays of 16 preparations, a mathematical relation between the biological potency and the NANA content, as an independent variable, was calculated. Membrane electrophoresis in Veronal-formamide buffer revealed a sharp band pattern, which could be explained by assuming a polymorphous HCG molecule, differing mainly in the number of terminal NANA groups. The prospects of a chemical assay of HCG based on the determination of NANA are, however, not at all encouraging.


2013 ◽  
Vol 680 ◽  
pp. 141-144 ◽  
Author(s):  
Qing Ye Liu ◽  
Gui Qing Wen ◽  
Kun Li ◽  
Ai Hui Liang

In pH 6.6 Na2HPO4- citric acid buffer solution and in the presence of KCl, the immunoreaction between hCG and nanosilver-labeled anti-hCG took place, the immunonanosilver-complex was formed and deposited, caused the resonance Rayleigh scattering (RRS) intensity at 510 nm decreased. In the optimal condition, the decreased RRS intensity responds linearly with the concentration of hCG over 0.125-1.75 µg/mL. Based on this, a new and simple RRS method has been proposed for the determination of hCG in serum samples, with satisfactory results.


2020 ◽  
Vol 32 (2) ◽  
pp. 177
Author(s):  
K. Hazano ◽  
S. Haneda ◽  
M. Matsui

In cattle, human chorionic gonadotrophin (hCG) is administered at Day 5 post-ovulation to improve fertility. This treatment can induce ovulation of the first-wave dominant follicle (W1DF), from which an accessory corpus luteum (CL) is generated. In addition, hCG has the effect of promoting CL development. It is possible that the locational relationship between the original and accessary CLs influences the effect of hCG on CL development, because the locational relationship of the CLs affects intraovarian blood flow. The present study aimed to clarify whether the locational relationship between the original and accessory CLs influences the effect of hCG on their development. Cross-bred beef heifers (Holstein×Japanese Black, n=56) were used for the present study. The oestrus cycle was synchronized using oestradiol benzoate (EB) and a controlled internal drug release (CIDR)-based program. Briefly, an administration of EB (2mg) with 9-day CIDR insertion was followed by administration of prostaglandin F2a analogue (PGF2a) on the day of CIDR removal, EB (1mg) 1 day after a PGF2a injection, and GnRH 12h after the second EB injection. At Day 5 post-ovulation, the locational relationship between the original CL and the W1DF was confirmed using transrectal ultrasonography (USG), and two groups were defined: ipsilateral group (IG; n=30), in which the CL and the W1DF are in the same ovary, and contralateral group (CG; n=26), in which the CL and the W1DF are in separate ovaries. Moreover, IG and CG were respectively subdivided into two groups, with or without hCG (1500IU) treatment (IG/hCG, n=15; IG without hCG, n=15, and CG/hCG, n=14; CG without hCG, n=12). The diameter and luteal tissue area (i.e. minus the cavity area) of the original CL and the accessory CL were examined at Days 5, 7, and 14, using USG. Two-way repeated-measures ANOVA was used to compare the diameter and luteal tissue area between IG/hCG and IG without hCG, and between CG/hCG and CG without hCG. In CG, the diameter (P<0.01) and luteal tissue area of the original CL (P<0.001) at Day 7 was increased by receiving hCG, while it did not change in IG. The diameter and luteal tissue area of the original CL at Day 14 were not affected by the administration of hCG in either CG or IG. Moreover, for the accessory CL, no difference of the diameter and luteal tissue area was observed between CG and IG. The present study showed that hCG treatment at Day 5 post-ovulation stimulate the growth of the original CL at Day 7, when the original CL and accessory CL are on contralateral sides. Our results suggest that the effect of administration of the hCG at Day 5 post-ovulation on the original CL development depends on the locational relationship between the original and accessory CL (IG or CG). The function of the CL affects the intrauterine environment for embryonic development. Therefore, it is necessary to investigate the effect of the hCG injection at Day 5 on the function of CL (i.e. plasma P4 concentration) in IG and CG, respectively.


1975 ◽  
Vol 64 (1) ◽  
pp. 117-123 ◽  
Author(s):  
BRUCE HOBSON ◽  
LEIF WIDE

SUMMARY Human chorionic gonadotrophin (HCG) was assayed by biological and radioimmunological methods in placentae from 16 women with a normal twin pregnancy. When the concentration and total amount of HCG in placentae was related to the sex of the twin foetus, no significant difference between 'male' and 'female' placentae was found. This is contrary to findings that there is a significant (P < 0·005) difference in the concentration of HCG per g and per placenta of singletons at term. A comparison between the grouped geometric mean data from bioassays shows that the amount of HCG per g and per placenta falls between the geometric mean values for 'male' and 'female' singleton placentae.


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