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since its a temp boost u know?
What I have always thought is that getting your natural Endogenous hormones back to balance was a very slow process. IMO HCG's role is to increase natural test allowing your body to come down from high levels instead of making your body fight its way up from low levels. Shock thos testes back to life
since its a temp boost u know?
I think if those herbs raised test they would suppress parts of the HPTA as well, to some degree. The body seeks homeostasis. HCG hasn't been shown to be suppressive in itself. It's the testosterone and estrogen it stimulates that is suppressive.hCG isn't a test booster like you are thinking...Test boosters are (ex.) trib,longjack, etc...They will not surpess you HPTA like hCG will...
I think if those herbs raised test they would suppress parts of the HPTA as well, to some degree. The body seeks homeostasis. HCG hasn't been shown to be suppressive in itself. It's the testosterone and estrogen it stimulates that is suppressive.
My understanding was that it suppresses LH,
J Clin Endocrinol Metab. 1989 Jul;69(1):170-6.
Inability to demonstrate an ultrashort loop feedback mechanism for luteinizing hormone in humans.
Kyle CV, Griffin J, Jarrett A, Odell WD.
Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City 84132.
hCG has biological properties similar to those of LH, but can be measured separately from LH by current radioimmunometric assays. To investigate the possible existence of an autoregulatory mechanism for LH in humans, we compared the basal LH concentrations and the LH response to a GnRH stimulus with and without prior administration of hCG. On two separate occasions, at least 1 week apart, six normal (eugonadal) males and six normal postmenopausal females were given, in random order, either 10,000 IU hCG or saline followed by iv injection of a 200-micrograms bolus of GnRH. Blood samples were then taken 30, 60, 90, 120, 180, 240, and 300 min after GnRH. Serum concentrations of LH and hCG were measured at each time by two monoclonal antibody sandwich assays developed in our laboratory. After exogenous hCG, serum hCG concentrations rose rapidly to 200-500 IU/L (15,000-35,000 pg/mL) in both the men and women, remaining at this high level throughout the study. In the men, sex steroid concentrations did not change in response to the hCG during the 9 study hours. Compared to saline-treated controls, hCG had no significant effect in either men or postmenopausal women on the basal LH concentration or the response to a GnRH bolus, as determined by peak response and area under the LH/time curve between 0-300 min after GnRH. We conclude that an ultrashort loop feedback mechanism for LH on its own secretion does not exist in humans, as assessed by the present protocol.
J Assist Reprod Genet. 1992 Apr;9(2):124-7.
Endogenous luteinizing hormone surges following administration of human chorionic gonadotropin: further evidence for lack of loop feedback in humans.
Nader S, Berkowitz AS.
Department of Obstetrics, Gynecology and Reproductive Sciences, University of Texas Medical School, Houston 77030.
The existence of inhibitory short- and ultrashort-loop feedback mechanisms for luteinizing hormone (LH), while documented in animals, has been questioned in humans. Since human chorionic gonadotropin (hCG) binds to LH receptors but can be distinguished from LH in immunoassays, it is possible to identify LH surges in the face of exogenously administered hCG. The present study demonstrates LH surges at midcycle in normal volunteers and in women undergoing controlled ovarian hyperstimulation, given hCG. This provides further evidence for lack of loop feedback control of LH secretion in humans.
I would run the hCG thruout the cycle to keep my testes in check DURING the cycle...This makes it easeir for the HPTA to get back to norm...
My understanding is that it doesn't seem to.
J Clin Endocrinol Metab. 1989 Jul;69(1):170-6.
Inability to demonstrate an ultrashort loop feedback mechanism for luteinizing hormone in humans.
Kyle CV, Griffin J, Jarrett A, Odell WD.
Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City 84132.
hCG has biological properties similar to those of LH, but can be measured separately from LH by current radioimmunometric assays. To investigate the possible existence of an autoregulatory mechanism for LH in humans, we compared the basal LH concentrations and the LH response to a GnRH stimulus with and without prior administration of hCG. On two separate occasions, at least 1 week apart, six normal (eugonadal) males and six normal postmenopausal females were given, in random order, either 10,000 IU hCG or saline followed by iv injection of a 200-micrograms bolus of GnRH. Blood samples were then taken 30, 60, 90, 120, 180, 240, and 300 min after GnRH. Serum concentrations of LH and hCG were measured at each time by two monoclonal antibody sandwich assays developed in our laboratory. After exogenous hCG, serum hCG concentrations rose rapidly to 200-500 IU/L (15,000-35,000 pg/mL) in both the men and women, remaining at this high level throughout the study. In the men, sex steroid concentrations did not change in response to the hCG during the 9 study hours. Compared to saline-treated controls, hCG had no significant effect in either men or postmenopausal women on the basal LH concentration or the response to a GnRH bolus, as determined by peak response and area under the LH/time curve between 0-300 min after GnRH. We conclude that an ultrashort loop feedback mechanism for LH on its own secretion does not exist in humans, as assessed by the present protocol.
Quote:
J Assist Reprod Genet. 1992 Apr;9(2):124-7.
Endogenous luteinizing hormone surges following administration of human chorionic gonadotropin: further evidence for lack of loop feedback in humans.
Nader S, Berkowitz AS.
Department of Obstetrics, Gynecology and Reproductive Sciences, University of Texas Medical School, Houston 77030.
The existence of inhibitory short- and ultrashort-loop feedback mechanisms for luteinizing hormone (LH), while documented in animals, has been questioned in humans. Since human chorionic gonadotropin (hCG) binds to LH receptors but can be distinguished from LH in immunoassays, it is possible to identify LH surges in the face of exogenously administered hCG. The present study demonstrates LH surges at midcycle in normal volunteers and in women undergoing controlled ovarian hyperstimulation, given hCG. This provides further evidence for lack of loop feedback control of LH secretion in humans.
There might be more to the story. In that case someone who knows please comment.
I agreeI would run the hCG thruout the cycle to keep my testes in check DURING the cycle...This makes it easeir for the HPTA to get back to norm...
LIPS
you are in correct here, here is my supportIf you take hCG as a PCT, in my opinon you are just pissing in the wind...Why?...Becasue you are still keeping your pituitary and hypothalamus supressed, even tho you still are making your balls produce the test...Keep you balls thruout the WHOLE cycle and you will find that when you do PCT it's a more effeicent way of comming back...Again, hCG will supress the HPTA just like steroids...In my opioon you don't want to do hCG as a post cycle thearpy or as a "test booster"!...It's not going to help your HPTA recover, it will supress just like steroids...
LIPS
Good post. If this is correct, wouldn't it be wise to just use hCG for PCT alone? Instead of taking PCT ancillaries, which have side effects, just use the hCG. Especially if it's not suppressive whatsoever. Any ideas on this?
.
i agree
a protocol i have read while on is 250iu every other day - also goes well with HMG 15iu EOD
My understanding is that it doesn't seem to.
Good post. If this is correct, wouldn't it be wise to just use hCG for PCT alone? Instead of taking PCT ancillaries, which have side effects, just use the hCG. Especially if it's not suppressive whatsoever. Any ideas on this?
.