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Nathan Goodyear

Long-term effect of ciprofloxacin on tes... [Int J Fertil Steril. 2013] - PubMed - NCBI - 0 views

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    mouse study finds that long-term cipro can lead to biochemical disruption of the testicles resulting in infertility, effected sperm counts, and decreased Testosterone.
Nathan Goodyear

Implications of adiponectin in linking metabolism ... [Endocrine. 2013] - PubMed - NCBI - 0 views

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    Adiponectin is negatively associated with LH, FSH production at the level of the pituitary and Testosterone at the level of the testicle.  Meaning: a risking adiponectin, as found in obesity, is associated with a down regulated HPA stimulation and Testosterone production.  This study, however, found a local autocrine/paracrine effect on sperm that was quite the opposite.
Nathan Goodyear

Phthalate-Induced Pathology in the Foetal Testi... [Reproduction. 2013] - PubMed - NCBI - 0 views

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    This study found a 2 fold increased in estradiol levels in rats exposed to phthalates in-utero.  This could have been due to increased aromatase activity and/or xenoestrogenic effect.  This study proposes a link between phthalate exposure in-uteruo, increased estrogen production and testicular dysgenesis syndrome.  Take home: in this model male testicles were altered prior to birth by phthalate exposure.
Nathan Goodyear

PLOS ONE: The Gut Microbiota and Developmental Programming of the Testis in Mice - 0 views

  • The intra-testicular level of testosterone in GF mice was found to be significantly lower than in SPF and CBUT mice
  • This study establishes a novel role for the commensal gut microbiota in the regulation of testicular development and function
  • Absence of the normal microbiota influences the formation and the integrity of the BTB as well as the intra-testicular levels of testosterone and serum levels of LH and FSH.
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  • Nutritional, socioeconomic, lifestyle and environmental factors (among others) are involved in the regulation of normal spermatogenesis.
  • he gut microbiota is one such potential source of environmental factors/products that has developed an intimate symbiotic relationship with host's physiology.
  • Manipulation of the gut microbiotia through dietary modification, pre- and probiotics can therefore be beneficial for the host's reproductive health.
  • In the current study, colonizing GF mice with CBUT resulted in an increased sperm production, suggesting that bacterial products, e.g. of fermentation, directly or indirectly, can affect the testis.
  • the absence of gut microbiota influenced testosterone levels
  • A recent study demonstrated that dietary supplementation of the probiotics Lactobacillus reuteri increased and restored testosterone levels in aging mice
  • bacterial metabolites such as butyrate have been shown to increase the levels of LH [43] and FSH
  • This suggests that butyrate most likely regulates testosterone production at the testicular level by stimulation of gene expression in Leydig cells and with little or no effect at the pituitary- hypothalamic levels.
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    gut micro biome effects spermatogenesis, Testosterone production, and the brain-testicle-barrier.
Nathan Goodyear

Sexual dysfunction in males with chronic hepatitis C and antiviral therapy: interferon-... - 0 views

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    Study of men with hepatitis C and interferon therapy found decrease in free and total Testosterone levels in men.  The study results suggest a non-HPA effect, which suggests more of a peripheral effect at the level of the TEsticles.
Nathan Goodyear

Testosterone for the aging male; current evidence and recommended practice - 0 views

  • Total serum testosterone consists of free testosterone (2%–3%), testosterone bound to sex hormone binding globulin (SHBG) (45%) and testosterone bound to other proteins (mainly albumin −50%)
  • Testosterone binds only loosely to albumin and so this testosterone as well as free testosterone is available to tissues and is termed bioavailable testosterone
  • Testosterone bound to SHBG is tightly bound and is biologically inactive
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  • Bioavailable and free testosterone are known to correlate better than total testosterone with clinical sequelae of androgenization such as bone mineral density and muscle strength
  • peak levels seen in the morning following sleep, which can be maintained into the seventh decade
  • Samples should always be taken in the morning before 11 am
  • The reliable measurement of serum free testosterone requires equilibrium dialysis. This is not appropriate for clinical use as it is very time consuming and therefore expensive.
  • With increasing age, a greater number of men have total testosterone levels just below the normal range or in the low-normal range. In these patients total testosterone can be an unreliable indicator of hypogonadal status.
  • It is advised that at least two serum testosterone measurements, taken before 11 am on different mornings, are necessary to confirm the diagnosis.
  • Patients with serum total testosterone consistently below 8 nmol/l invariably demonstrate the clinical syndrome of hypogonadism and are likely to benefit from treatment. Patients with serum total testosterone in the range 8–12 nmol/l often have symptoms attributable to hypogonadism and it may be decided to offer either a clinical trial of testosterone treatment or to make further efforts to define serum bioavailable or free testosterone and then reconsider treatment. Patients with serum total testosterone persistently above 12 nmol/l do not have hypogonadism and symptoms are likely to be due to other disease states or ageing per se so testosterone treatment is not indicated.
  • Total testosterone levels fall at an average of 1.6% per year whilst free and bioavailable levels fall by 2%–3% per year.
  • With advancing age there is also a reduction in androgen receptor concentration in some target tissues and this may contribute to the clinical syndrome of LOH
  • Metabolic clearance declines with age
  • Gonadotrophin levels rise during aging (Feldman et al 2002) and testicular secretory responses to recombinant human chorionic gonadotrophin (hCG) are reduced
  • There are changes in the lutenising hormone (LH) production which consist of decreased LH pulse frequency and amplitude, (Veldhuis et al 1992; Pincus et al 1997) although pituitary production of LH in response to pharmacological stimulation with exogenous GnRH analogues is preserved
  • the decreases in testosterone levels with aging seem to reflect changes at all levels of the hypothalamic-pituitary-testicular axis
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    Leptin inhibits male Testosterone production at the level of the hypothalamus and at the testicle level.
Nathan Goodyear

Direct Inhibitory Effect of Glucocorticoids upon Testicular Luteinizing Hormone Recepto... - 0 views

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    glucocorticoids inhibit Testosterone production via down regulation of LH receptors at the level of the testicles.
Nathan Goodyear

Induction of Testicular Aromatization by Luteinizing Hormone in Mature Rats - 0 views

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    very interesting study in rats.  LH induced a dose-dependent increase in testicular estrogen production through aromatase activity.  Yes, LH stimulates the leydig cells to produce testosterone, but there is a point at which LH will actually increase aromatase activity and thus estrogen production at the testicular level.
Nathan Goodyear

Aging and Luteinizing Hormone Effects on Reactive Oxygen Species Production and DNA Dam... - 0 views

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    Interesting rat model finds that stimulation of the leydig cells of the testis by LH induces ROS.  May be one of the mechanisms by which androgen therapy will induce long-term requirement for replacement.
Nathan Goodyear

Functional Importance of 1α,25(OH)2-Vitamin D3 and the Identification of Its ... - 0 views

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    Vitamin D plays role in healthy Testes function.  This signaling occurs through genomic and non-genomic signaling pathways.  Testosterone production is influenced, sperm motility and spermatogenesis is influenced.  
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