Testosterone is anti-inflammatory

The effect of testosterone replacement on endogenous inflammatory cytokines and lipid profiles in hypogonadal men

J Clin Endocrinol Metab. 2004 Jul;89(7):3313-8

Malkin CJ, Pugh PJ, Jones RD, Kapoor D, Channer KS, Jones TH.

Abstract

Testosterone has immune-modulating properties, and current in vitro evidence suggests that testosterone may suppress the expression of the proinflammatory cytokines TNF-alpha, IL-1beta, and IL-6 and potentiate the expression of the antiinflammatory cytokine IL-10.

We report a randomized, single-blind, placebo-controlled, crossover study of testosterone replacement (Sustanon 100) vs. placebo in 27 men (age, 62 +/- 9 yr) with symptomatic androgen deficiency (total testosterone, 4.4 +/- 1.2 nmol/liter; bioavailable testosterone, 2.4 +/- 1.1 nmol/liter).

Compared with placebo, testosterone induced reductions in TNFalpha (-3.1 +/- 8.3 vs. 1.3 +/- 5.2 pg/ml; P = 0.01) and IL-1beta (-0.14 +/- 0.32 vs. 0.18 +/- 0.55 pg/ml; P = 0.08) and an increase in IL-10 (0.33 +/- 1.8 vs. -1.1 +/- 3.0 pg/ml; P = 0.01); the reductions of TNFalpha and IL-1beta were positively correlated (r(S) = 0.588; P = 0.003).

In addition, a significant reduction in total cholesterol was recorded with testosterone therapy (-0.25 +/- 0.4 vs. -0.004 +/- 0.4 mmol/liter; P = 0.04).

In conclusion, testosterone replacement shifts the cytokine balance to a state of reduced inflammation and lowers total cholesterol. Twenty of these men had established coronary disease, and because total cholesterol is a cardiovascular risk factor, and proinflammatory cytokines mediate the development and complications associated with atheromatous plaque, these properties may have particular relevance in men with overt vascular disease.

PMID: 15240608

 

Testosterone optimization has multiple mechanisms for improving depression, including:

• Suppressing pro-inflammatory cytokines TNF-alpha, IL-1-beta, and iL-6

• Increasing Anti-inflammatory cytokine IL-10

• Improving dopamine signaling

• Improving activation of thyroid hormone (from T4 to T3)

• Improving estradiol (which when optimal, increases BDNF, improves ability to form synapses, improves norepinephrine, dopamine, and serotonin signaling)

• Increasing IGF-1 (which provides most of the effects of growth hormone)

• Suppressing excessive norepinephrine signaling

• Helping reduce visceral fat

• Reducing insulin resistance

• Improving coronary artery blood flow

• etc.

Once the foundation is set to negate potential negative effects, Testosterone is a viable option for treating depression in men with hypogonadism.  

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