***NOTE: I CREATED A NEW THREAD FOR THIS DISCUSSION
https://raypeatforum.com/community/threads/methylene-blue-and-androgen-synthesis.13457/***
In reference to the sentence in the below abstract that reads:
'This is further supported by c-PTIO countering the inhibitory action of methylene blue on androgen synthesis.'
I couldn't find any studies that discussed the inhibitory action of Methylene Blue on androgen synthesis. Any insight would be appreciated...Thanks
http://www.sciencedirect.com.proxy1.athensams.net/science/article/pii/S0041008X00990793
Decreased Steroid Hormone Synthesis from Inorganic Nitrite and Nitrate: Studies in Vitro and in Vivo
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Nirmal S. Panesar 1, Kam W. Chan
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doi:10.1006/taap.2000.9079
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Abstract
Nitrites and nitrates are consumed nonchalantly in diet. Organic nitrates are also used as vasodilators in angina pectoris, but the therapy is associated with tolerance whose mechanism remains elusive. Previously, we found inorganic nitrate inhibited steroidogenesis in vitro. Because adrenocorticoids regulate water and electrolyte metabolism, tolerance may ensue from steroid deficiency. We have studied the effects of nitrite and nitrate on in vitro synthesis and in vivo blood levels of steroid hormones. In vitro, nitrite was more potent than nitrate in inhibiting human chorionic gonadotropin (hCG)-stimulated androgen synthesis by Mouse Leydig Tumor cells. At concentrations above 42 mM, nitrite completely inhibited androgen synthesis, and, unlike nitrate, the inhibition was irreversible by increasing hCG concentration. The cAMP production remained intact but reduced with both ions. The nitric oxide (NO) scavenger, 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxy-3-oxide (c-PTIO) significantly increased hCG- or cAMP-stimulated androgen synthesis in all buffers, suggesting that NO is a chemical species directly involved in the nitrite/nitrate-induced inhibition. This is further supported by c-PTIO countering the inhibitory action of methylene blue on androgen synthesis. Rats given distilled water containing 50 mg/L NaNO2 or NaNO3 for 4 weeks drank significantly less daily. At the end, their blood corticosterone and testosterone levels were significantly decreased. The adrenocortical histology showed bigger lipid droplets, which are pathogonomic of impaired steroidogenesis. Nitrite and nitrate are metabolized to NO, which binds heme in cytochrome P450 enzymes, thereby inhibiting steroidogenesis. Therapeutic nitrates likewise may decrease adrenal (and gonadal) steroidogenesis. Cortisol deficiency would impair water excretion causing volume expansion, and aldosterone deficiency would cause sodium loss and raised renin. Paradoxically, volume expansion without sodium retention and raised renin has all been reported in tolerance.
https://raypeatforum.com/community/threads/methylene-blue-and-androgen-synthesis.13457/***
In reference to the sentence in the below abstract that reads:
'This is further supported by c-PTIO countering the inhibitory action of methylene blue on androgen synthesis.'
I couldn't find any studies that discussed the inhibitory action of Methylene Blue on androgen synthesis. Any insight would be appreciated...Thanks
http://www.sciencedirect.com.proxy1.athensams.net/science/article/pii/S0041008X00990793
Decreased Steroid Hormone Synthesis from Inorganic Nitrite and Nitrate: Studies in Vitro and in Vivo
Author links open the overlay panel. Numbers correspond to the affiliation list which can be exposed by using the show more link.
Nirmal S. Panesar 1, Kam W. Chan
Show more
doi:10.1006/taap.2000.9079
Get rights and content
Abstract
Nitrites and nitrates are consumed nonchalantly in diet. Organic nitrates are also used as vasodilators in angina pectoris, but the therapy is associated with tolerance whose mechanism remains elusive. Previously, we found inorganic nitrate inhibited steroidogenesis in vitro. Because adrenocorticoids regulate water and electrolyte metabolism, tolerance may ensue from steroid deficiency. We have studied the effects of nitrite and nitrate on in vitro synthesis and in vivo blood levels of steroid hormones. In vitro, nitrite was more potent than nitrate in inhibiting human chorionic gonadotropin (hCG)-stimulated androgen synthesis by Mouse Leydig Tumor cells. At concentrations above 42 mM, nitrite completely inhibited androgen synthesis, and, unlike nitrate, the inhibition was irreversible by increasing hCG concentration. The cAMP production remained intact but reduced with both ions. The nitric oxide (NO) scavenger, 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxy-3-oxide (c-PTIO) significantly increased hCG- or cAMP-stimulated androgen synthesis in all buffers, suggesting that NO is a chemical species directly involved in the nitrite/nitrate-induced inhibition. This is further supported by c-PTIO countering the inhibitory action of methylene blue on androgen synthesis. Rats given distilled water containing 50 mg/L NaNO2 or NaNO3 for 4 weeks drank significantly less daily. At the end, their blood corticosterone and testosterone levels were significantly decreased. The adrenocortical histology showed bigger lipid droplets, which are pathogonomic of impaired steroidogenesis. Nitrite and nitrate are metabolized to NO, which binds heme in cytochrome P450 enzymes, thereby inhibiting steroidogenesis. Therapeutic nitrates likewise may decrease adrenal (and gonadal) steroidogenesis. Cortisol deficiency would impair water excretion causing volume expansion, and aldosterone deficiency would cause sodium loss and raised renin. Paradoxically, volume expansion without sodium retention and raised renin has all been reported in tolerance.
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