A Combination of Fast-Clearance Nandrolone Plus Low-intensity Aerobic Exercise Improves RBC Indices in Anemic Aging Mice.

Abstract

Anemia is a common health disorder in the aging population. Conventional therapy to treat anemia with recombinant erythropoietin (rhEpo) has limitations for elderly patients in part because endogenous Epo increases with age even before, and rises further after, anemia becomes apparent [1]. Androgen therapy, the mainstay for anemia treatments before the advent of rhEpo, thus deserves a reevaluation. Low testosterone is not only a marker, but also can be a cause, of anemia in the elderly [2-4]. Androgen-induced erythropoiesis is a long-standing clinical observation recently recapitulated in rodent models. A main disadvantage of androgen therapy is the concern for cardiovascular risk [5]. Noticeably, most clinical and animal studies use esterified androgen to prolong the drug half-life, sustaining tissue exposure to supraphysiological androgen stimulation. This may contribute to cardiac hypertrophy, at least in animal models [6]. We thus tested the effect of intermittent injection of a fast-clearance androgen (unesterified nandrolone) on RBC indices in older mice which developed anemia as a consequence of aging. We also tested whether adding a routine low-intensity aerobic exercise may enhance the effect of this intervention. The study was conducted on male C57BL/6 mice of 26 28 months, corresponding to the 50-40% strain survival window. Twenty-four anemic mice (hematocrit 29-37%) were evenly divided into four groups as control (c), nandrolone (n), exercise (ex) and exercise plus nandrolone (nex). Nandrolone or vehicle (sesame oil) was injected twice per week (100 mg/kg, 100 ul, sc). Body composition, grip-strength and blood were measured before and after the experiment. Animals were trained twice per week as described [6]. Serum nandrolone concentration was measured three days after injection using MASS and estimated to be 250 1,000 ng/ dl within hours post injection but drop to 3 5 ng/dL after 48 h. The steady-state concentration was substantially lower than serum testosterone propionate injected at half the dose [6]. To confirm that the nandrolone was functional, we performed Western analysis for splenic nuclear androgen receptor (AR). In the absence of androgenic ligands, AR is targeted to degradation without nuclear accumulation. As shown in Figure 1A, nuclear AR was undetected in control animals. At 24 h post injection, nandrolone increased nuclear AR but to a lesser extent compared to that induced by testosterone propionate, suggesting that nandrolone is sufficient to activate AR without sustaining high androgen concentrations in circulation. Treatment with nandrolone for two months did not change skeletal and cardiac muscle mass (not shown), compared to 30% historic increase of each after treatment with testosterone propionate following otherwise identical experimental protocols [6]. Changes in RBC indices for each animal were obtained by subtracting the baseline data from the final measurements. A numerical increase in hemoglobin (HgB) was induced by exercise and more by nandrolone; but each did not reach statistical significance. A combination of exercise and nandrolone, however, induced a significant increase in HgB (Fig. 1B). Similar effect was observed for RBC and hematocrit (Fig. 1C, D). Serum iron was not different among the four groups (Fig. 1E) but transferrin saturation (TSAT) was similarly increased by each intervention (Fig. 1F). TSAT is a measure of transferrin-bound iron, the major source of hemoglobin iron. Finally, we assessed the effect of each intervention on grip-strength for functional assessment. As shown in Figure 1G, grip-strength at baseline was somewhat higher in the control group. Two months later, all animals showed age-related loss in grip-strength, but this loss was attenuated by about 50% in animals that went through exercise or nanManuscript accepted for publication October 11, 2013