Examples of using Gnrh in English and their translations into German
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They are called GnRh analogues.
Directed at working against the GnRH.
What is GnRH(gonadotropin-releasing hormone)?
This increases the levels of GnRH, LH and FSH.
GnRH agonists are first-choice drugs in endocrine therapy.
People also translate
These include the hormones GnRH, GHRH, TRH and CRH.
GnRH is released in a pulsatile fashion in the postpubertal adult.
Gonadorelin is another name for gonadotropin-releasing hormone GnRH.
GnRH(Gonadotrope Releasing Hormone) is strongly reduced or stopped.
Some data suggest that the decreased release of hypothalamic GnRH into the pituitary is responsible for the suppressed level of LH.
Another GnRH analogue has been shown to be foetotoxic in laboratory animals.
Spontaneous ovulation during the cycle is typically prevented by the use of GnRH agonists or GnRH antagonists, which block the natural surge of luteinising hormone LH.
GnRH Antagonist Medicaton, that suppresses own production of FSH and LH.
Long- term administration results in pituitary desensitisation to the effects of GnRH resulting in a suppression of LH and FSH secretion by the pituitary.
Excretion of GnRH(Gonadotrope releasing hormone) is strongly reduced or stopped.
The active substance in Firmagon, degarelix, is a gonadotrophin-releasing hormone antagonist, which means thatit blocks the effects of a natural hormone called gonadotrophin-releasing hormone GnRH.
GnRH sends a signal to the second level of the axis, the pituitary, which releases Luteinizing Hormone in response.
Orgalutran was compared with buserelin, leuprorelin, and triptorelin these medicines are GnRH agonists: they act on the secretion of LH by stimulating the production of GnRH to such an extent that the body stops making LH.
GnRH, acting on the anterior pituitary, stimulates the synthesis and secretion of follicle-stimulating and luteinizing hormone in the same intermittent mode.
According to scientific study that has been conducted on animal testsubjects, it has been determined that GnRH(Triptorelin)'s chief function is to lower the expression of luteinizing hormone and follicle-stimulating hormone.
The reason is that if GnRH from the hypothalamus does not episodically affect the pituitary gland, the activity of the latter will be down-regulated.
Combined forms of hormonal contraception contain ethinyl estradiol and a progestin,which both contribute to the inhibition of GnRH, LH, and FSH, which accounts for the ability of these birth control methods to prevent ovulation and thus prevent pregnancy.
At the pituitary, GnRH stimulates the synthesis and secretion of the gonadotropins, follicle-stimulating hormone(FSH), and luteinizing hormone LH.
Orgalutran should not be used in people who may be hypersensitive(allergic) to ganirelix, to any of the other ingredients, to GnRH or to other GnRH analogues medicines that have a similar structure to GnRH and modify the activity of GnRH in the body.
Thus a single hormone, GnRH, controls a complex process of follicular growth, ovulation, and corpus luteum maintenance in the female, and spermatogenesis in the male.
The Committee also noted that treatment with Firmagon does not trigger the temporary sharp rise in testosterone levels seen with‘ GnRH agonists' other medicines for prostate cancer that stimulate the production of GnRH.
Studies found that GnRH agonists given for endometriosis patients undergoing in-vitro fertilization cycles improves significantly their fertility and decreases preclinical abortions.
Orgalutran was compared with buserelin, leuprorelin, and triptorelin GnRH agonists: another group of medicines used to prevent premature ovulation, which work by stimulating the receptor for GnRH to such an extent that the body stops making LH.
GnRH analogues are substances which are derived from natural gonatropine-releasing hormone(GnRH) Natural GnRH is transmitted from the brain to the pituitary gland, where it stimulates formation and secretion of the gonatropines and, ultimately, the ovaries.
Because of the way in which GnRH(Triptorelin) can function in conjunction with hormone-related secretions, scientific study based on animal test subjects has determined that its presence can theoretically make it useful in the treatment of specific kinds of hormone responsive cancers, such as prostate and breast cancers.
