Treatment of Aplastic Anemia with Nandrolone DecanoateGenerates cardiac autonomic dysfunction, not reversible after the interruption of treatment. Anabolic androgenic steroids are a class of synthetic compounds derived from testosterone, eventually used by athletes, to nandrolone treatment physical performance. However, anabolic steroids can also modify normal cardiovascular function. Thus, we investigated cardiac electrophysiological and autonomic abnormalities in rats, through a electrocardiographic variability protocol during and nandrolone treatment interruption of administration of nandrolone decanoate DECA stanozolol tabletten 10 mg steroid. Body mass was lower in treated rats compared to control after 4th and 8th weeks, but not at the end of 14th nandrolone treatment. Cardiac autonomic dysfunction vagal attenuation was present on DECA group after 4th week and did not normalize nandrolone treatment interruption of treatment.
Nandrolone - Wikipedia
Shehzad Basaria, Justin T. The purpose of this study was to review the preclinical and clinical literature relevant to the efficacy and safety of anabolic androgen steroid therapy for palliative treatment of severe weight loss associated with chronic diseases. Data sources were published literature identified from the Medline database from January to December , bibliographic references, and textbooks.
Reports from preclinical and clinical trials were selected. Study designs and results were extracted from trial reports. Statistical evaluation or meta-analysis of combined results was not attempted.
Androgenic anabolic steroids AAS are widely prescribed for the treatment of male hypogonadism; however, they may play a significant role in the treatment of other conditions as well, such as cachexia associated with human immunodeficiency virus, cancer, burns, renal and hepatic failure, and anemia associated with leukemia or kidney failure. A review of the anabolic effects of androgens and their efficacy in the treatment of these conditions is provided.
In addition, the numerous and sometimes serious side effects that have been known to occur with androgen use are reviewed. Although the threat of various side effects is present, AAS therapy appears to have a favorable anabolic effect on patients with chronic diseases and muscle catabolism. We recommend that AAS can be used for the treatment of patients with acquired immunodeficiency syndrome wasting and in severely catabolic patients with severe burns.
Preliminary data in renal failure-associated wasting are also positive. Advantages and disadvantages should be weighed carefully when comparing AAS therapy to other weight-gaining measures. Although a conservative approach to the use of AAS in patients with chronic diseases is still recommended, the utility of AAS therapy in the attenuation of severe weight loss associated with disease states such as cancer, postoperative recovery, and wasting due to pulmonary and hepatic disease should be more thoroughly investigated.
In , French physiologist Charles Edouard Brown-Sequard announced that an extract of dog and guinea pig testicles given iv results in an increase in physical strength, improvement in intellectual energy, relief of constipation, and lengthening of the arc of his urine. In the late s the anabolic agent responsible for these effects, the androgens, were isolated.
Although initially used by body builders, the positive results encouraged AAS use in other strength-intensive sports, including football, track and field, hockey, swimming, soccer, cycling, volleyball, and wrestling.
Anabolic-androgenic steroids AAS have also been used in clinical practice since the s in the treatment of chronic debilitating illnesses, trauma, burns, surgery, and radiation therapy 1 — 4.
The effects on hematological parameters were recognized as early as , and before bone marrow transplantation and the use of synthetic erythropoietin became common, AAS were often used to treat various types of anemias 5.
Norethandrolone and methandrostenolone [Dianabol discontinued in ; CIBA, New Jersey] also became available on the market during the s.
The psychoactive effects of AAS broadened its use to treat depression and melancholia. However, cachexia is prevalent in a wide spectrum of chronic diseases, including chronic renal failure, hepatic cirrhosis, cancer, and pulmonary disease. Although increased caloric intake and an exercise regimen are of paramount importance in the maintenance of body weight, treatment with anabolic agents may enhance the effects of these measures.
AAS therapy does have several clinical uses other than androgen replacement. These applications are not discussed in this review. Instead, we focus primarily on the anabolic properties of these agents in patients with debilitating conditions. T is a steroid hormone synthesized primarily in the Leydig cells of the testes in men; however, it is also present in women, in whom it is synthesized in the ovaries and adrenal glands.
Its synthesis is stimulated by the action of LH, which in men, targets testicular Leydig cells resulting in an increase in cAMP production. This, in turn, enhances the activity of the enzymes needed for T synthesis and increases the availability of their primary substrate, cholesterol.
This is followed by a cascade of enzymatic reactions that yields T as the final product. Healthy adult men produce between 2. DHT has a relatively higher receptor binding affinity of 0. Estimates of the relative potency of DHT to T have ranged from 2: Likewise, the dissociation constant for DHT is 0.
In women, T is secreted by the ovaries and adrenal glands. The majority of T produced in women is converted to E2 in adipocytes by the enzyme aromatase. Since T in its native form is rapidly absorbed and degraded regardless of the route used, the use of modified analogs has become a favored method of androgen administration. There are three main classes of androgen analogs. Longer carbon chains in these groups yield androgen derivatives that are more soluble in lipid vehicles, such as those used for im injection.
T, when injected as a solution in oil, is rapidly absorbed, metabolized, and excreted. T esters are less polar and are absorbed slowly when injected im in oil.
Different esters have variable durations of action, and therefore the frequency of T administration depends on the type of ester being used. T propionate is given two or three times weekly, T cypionate and enanthate are effective when given at 2- to 4-wk intervals, and T buciclate can be administered at wk intervals 6.
Class C analogs are those that are produced via modification of the A, B, or C rings, such as mesterolone. These analogs often exist in conjunction with those of class A as AC analogs Table 1. T is inactivated primarily by the cytochrome P family of hepatic isoenzymes. Therapeutic preparations of T have been developed to circumvent this immediate metabolism.
Class A derivatives have long alkyl side-chains, rendering them less polar than T and hence retarding their hepatic metabolism and increasing their half-life in the peripheral tissues. They are, however, eventually hydrolyzed and metabolized by the same pathway as endogenous T. The modification in the class B and C derivatives alters their metabolic pathway, yielding a longer half-life. They are variably excreted either unaltered or as metabolites and conjugates in the urine or feces 5.
For decades researchers have known the anabolic potential of androgens. This made the use of androgens popular among athletes.
However, it was soon noted that these agents along with being anabolic, also result in androgenic side effects such as acne and increased sebum production in men and hirsutism and even virilization in women. For years, scientists have labored to dissociate anabolic from androgenic effects with the hope of producing a purely anabolic agent that is free from any androgenic side effects.
Unfortunately, to date no such compound exists. Androgens are a group of biologically diverse compounds with a variety of effects anabolic and androgenic in different body tissues 7. The androgenic effects of AAS include induction of male phenotype starting from sexual differentiation in utero , growth of sexual organs genitals and prostate , development of secondary sexual characteristics, maintenance of sexual function, and fertility.
The anabolic effects of AAS include nitrogen retention and increases in muscle mass and strength. Although androgens mediate a broad range of developmental and homeostatic function, all of the androgens induce their response via a single AR despite this diversity. Attempts in the past have failed to isolate a pure anabolic or a pure androgenic receptor 9. One explanation in the case of T is that it is a prohormone, and many of its actions in different tissues are mediated by its metabolites.
These analogs interact with the AR directly. These data show that the conversion of AAS in various tissues into different metabolites and the relative binding affinity of these metabolites to AR in these tissues are responsible for its diverse actions.
However, in a recent animal study, Hsiao et al. Therefore, it is possible that a selective androgen response element sequence may play a role in differential T vs.
DHT AR trans -activation. Many studies have shown that administration of androgens to hypogonadal young and elderly men results in an increase in lean body mass LBM 11 , However, interestingly, supraphysiological doses of T result in an increase in muscle mass and strength even in eugonadal men The positive response observed in these men even though the majority of ARs are likely to be saturated suggests that androgens also mediate anabolic effects indirectly, i.
Therefore, one can divide the anabolic actions of AAS into direct and indirect mechanisms. Administration of T to hypogonadal men results in an increase in both contractile and noncontractile skeletal muscle proteins. Increased incorporation of leucine into the skeletal muscle was observed in six hypogonadal men after 6 months of treatment with T cypionate All men had an increase in muscle mass from the baseline. Similarly, a single injection of mg T enanthate results in increased skeletal muscle protein synthesis and efficient utilization of amino acids In summary, androgens increase muscle mass and strength by increasing efficient utilization of amino acids and, at least in case of oxandrolone, by increasing AR expression in skeletal muscle.
Indirect evidence exists that the anabolic effects of androgens on skeletal muscle may be mediated by the antiglucocorticoid action of androgens. In vitro experiments have shown that T has a high affinity for GR The same group has also shown that T acts as an antagonist to endogenous circulating glucocorticoids These observations are appealing because there is a great degree of homology between AR and GR These observations are further supported by the fact that antagonism of glucocorticoids prevents muscle atrophy in men who have undergone orchidectomy Furthermore, administration of large doses of AAS to these men result in an increase in urinary free cortisol Men with androgen insensitivity syndrome also show nitrogen retention when given large doses of AAS despite having nonfunctional ARs Similarly, T administration to patients with severe burns a state of hypercortisolism and hypogonadism shows a significant decrease in protein breakdown Although the majority of the reports suggest GR antagonism as the main mode of androgen action, some have proposed that AAS interfere with glucocorticoid action at the gene level by interfering with hormone response elements Interaction with IGF-I system.
Intravenous infusion of IGF-I results in stimulation of skeletal muscle protein synthesis This is supported by the observation that induction of hypogonadism in normal young men results in a reduction in IGF-I mRNA levels in skeletal muscle Regulation of myostatin gene.
The effects of AAS at the genetic level are currently poorly understood. Recently, the human myostatin gene was cloned. This gene is located on chromosome 2 and is a negative regulator of muscle growth. Inactivating mutations of this gene in mice and cattle are associated with double muscling in these animals The myostatin protein is secreted into the serum and can be measured in the circulation. In a recent study, myostatin levels were elevated in the serum and skeletal muscle biopsy specimens of patients with AIDS associated sarcopenia compared with those in AIDS patients without any weight loss and normal controls Furthermore, high levels of circulating myostatin have produced muscle atrophy in the rat Preliminary research suggests that the myostatin protein may play a role in age-associated sarcopenia This is further supported by the fact that low gravity-induced muscle wasting accompanies an increase in myostatin mRNA As androgen levels decline with aging, it is possible that myostatin levels may rise as a result of andropause.