El Café de los Angelitos I

Posted on By tangopedia 82 comentarios en El Café de los Angelitos I
Carlos Gardel, historias, Lugares

Por Carlos Benitez1

Esquina de las calles Rivadavia y Rincón. Refugio de la barra de Gardel. Su dueño era el itálico don Bautista. Está ubicado en el barrio de la niñez de José Razzano (el Orientalito) y del célebre gordo Roberto Casaux, futuro experimentado actor cómico. A una cuadra se encuentra la Iglesia Regina Martyrun donde ambos compartían sus habilidades en el Coro.
A la mesa de ese bar concurrió toda la vida Alfredo De Ferrari, quien siempre contribuyó prestándole su viola al futuro célebre dúo Gardel-Razzano.

Con el tiempo el dúo empezó a “echar buena” y eran venerados en el Armenonville, célebre cabaret vidriado de la Av. Alvear. Era un templo de placer, primer ejemplar imitativo del cabaret-chateau parisiense. Ganaron cifras siderales. Allí solamente corría champagne y concurría la elite noble-bohemia de los años 13. Cobraban $70 por noche más las jugosas propinas de los Reservados.
Diametralmente opuesto al Armenonville, que era una ostentación al lujo, se constituía el modesto Café de los Angelitos. Allí concurría el dúo después de las extensas jornadas de trabajo a repartir las ganancias. Razzano era el cajero. Tenía plata por todos los bolsillos y Gardel lo revisaba por sí se guardaba algún billete, sucumbiendo a las tentaciones.
Más tarde, también vuelve a ser punto de encuentro después de actuar en los consagratorios teatros de la calle Corrientes. Allí siempre y desde un principio, aparte del dúo, componían la mesa chica los hermanos Alfredo y Armando de Ferrari, los hermanos Ernesto y Gabriel Laurent y Roberto Casaux. Antonio Sumaje, el aviador, dormitaba en el mateo. Él los transportaba en su coche de caballos, cambiando tiempo después el látigo por el volante. Fueron famosas las partidas de truco donde se ponía en juego quién garpaba los famosos bifes regados con tinto, que Don Bautista hacía marchar. Y sucedió lo previsible. La mesa se fue agrandando. Apareció el pensador Iglesias Paz, Joaquín de Vedia, el célebre jockey Manuel Lema, Manuel Bénard -uno de los creadores de SADAIC y de la ley 11723 de propiedad intelectual entre otras cosas-, un grandote Goliat Luis Ángel Firpo, el Toro Salvaje de las Pampas.
Gardel y Razzano cantaban en las sobremesas trovas de pampa y sierra. E increíblemente van llegando más hombres. Algunos de ellos son los mismos que Gardel oyera con mucho respeto en tiempos idos, cuando no se atrevía a abrir la boca estando ante semejantes troveros. Uno es Ezeiza, el famoso negro Gabino del Heroico Paysandú, otros Curlando, Ramoncito Vieytes, Higinio Cazón, el gurí cantos Aguiar, Ambrosio Ríos. Y un día apareció nada más y nada menos que Don José Betinotti para que el dúo cantara las primicias “Como quiere la madre a sus hijos” y “Tú Diagnóstico”. El Café de los Angelitos se estremecía con esas canciones.
Hay una ocurrencia de Manucho Güiraldes, hermano de Ricardo (autor de Don Segundo Sombra), del pago de Areco donde más de una vez cantó el dúo para el héroe de la novela Don Segundo Ramírez: llegó una vez al Café y vio al gigante boxeador Firpo, a Gabriel Laurent y Alfredo de Ferrari pasando los 120 Kg y palmeándole la espalda a Gardel con más de 100 kg y mirando el cartel del Bar le dijo “a éste café lo llaman de …los angelitos?”.

1 Coleccionista, Presidente del Círculo Gardeliano Bahiense, dueño y fundador del Museo de Radios Antiguas Carlos Gardel de Bahía Blanca.

Interpretación de Libertad Lamarque del Tango “Café de los Angelitos” de Cátulo Castillo y José Razzano

CAFÉ DE LOS ANGELITOS
(Cátulo Castillo y José Razzano)

Yo te evoco, perdido en la vida

Y enredado en los hilos del humo,

Frente a un grato recuerdo que fumo

Y a esta negra porción de café…

Rivadavia y Rincón… Vieja esquina

De la antigua amistad que regresa,

Coqueteando su gris, en la mesa

Que está,

Meditando en sus noches de ayer…

¡Café de los Angelitos!…

¡Bar de Gabino y Cazón!…

Yo te alegré con mis gritos

En los tiempos de Carlitos

Por Rivadavia y Rincón…

¿Tras de qué sueños volaron?…

¿En qué estrellas andarán?…

Las voces que ayer llegaron

Y pasaron y callaron,

¿Dónde están?…

¡Por qué calles volverán!…

Cuando llueven las noches su frío

Vuelvo al mismo lugar del pasado,

Y de nuevo se sienta a mi lado

Betinoti, templando su voz…

Y en el dulce rincón que era mío

Su cansancio la vida bosteza,

Porque nadie me llama a la mesa

De ayer…

¡Porque todo es ausencia y adiós!…

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82 thoughts on “El Café de los Angelitos I”

  4. Anavar Oxandrolone: Benefits, Side Effects, Dosage, And More

    Anavar (Oxandrolone): Benefits, Side Effects, Dosage,
    and More

    Anavar, the brand name for oxandrolone, is a well‑known anabolic steroid
    that has earned popularity among bodybuilders, athletes, and fitness enthusiasts.
    Its reputation stems from its relatively mild side‑effect
    profile compared to other steroids, making it a frequent choice for those looking to
    enhance performance while minimizing health risks.

    —

    Approved Testosterone Source

    Oxandrolone was originally developed as an oral testosterone derivative in the 1960s by the pharmaceutical company
    Searle Laboratories. It was approved by regulatory agencies for
    specific medical uses such as treating weight loss after surgery
    or trauma, and for correcting hormonal deficiencies.
    Despite its therapeutic origins, many users now obtain Anavar from non‑prescription sources, which can pose significant legal and safety
    concerns.

    —

    Anavar Benefits

    Fat Loss

    Anavar stimulates metabolic rate without drastically increasing cortisol levels.
    This helps the body burn stored fat while preserving
    lean tissue during calorie restriction or cutting phases.

    Muscle Gain

    Although modest compared to bulking steroids, oxandrolone promotes protein synthesis, leading to noticeable gains
    in muscle mass even at low doses.

    Strength Building

    Users often report a steady increase in strength, allowing for heavier lifts and improved overall performance without the harsh side effects associated
    with stronger anabolic agents.

    —

    Legal Steroid Alternatives That Work

    HMB (Beta‑hydroxy beta‑methylbutyrate) – Supports muscle preservation during caloric deficits.

    Creatine Monohydrate – Enhances power output and aids
    in quick recovery.

    Whey Protein Isolate – Provides high‑quality protein for
    muscle repair.

    These supplements can mimic many of Anavar’s benefits
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    Mild Side Effects

    Less Liver Toxic

    Because oxandrolone is a 17α‑alkylated compound, it
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    No Gynecomastia or Water Retention

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    Less Androgenicity

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    Less Problematic for Women

    Due to its lower androgenic effect, Anavar is considered one of the safest
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    Increased Recovery, Endurance, and Speed

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    Pronounced Pumps

    Oxandrolone can cause significant vascularity, giving athletes a “pump” effect that is
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    —

    Anavar Side Effects

    While mild compared to other steroids, anavar dosage for women bodybuilding still carries risks:

    High LDL Cholesterol – Can raise bad cholesterol levels if not monitored.

    Suppressed Testosterone – Prolonged use may lower
    natural testosterone production.

    Kidney Damage – Rare but possible with high doses or extended
    cycles.

    Hair Loss – Genetic predisposition can be exacerbated by anabolic steroid use.

    How to Prevent Hair Loss on Anavar

    Use Finasteride or Dutasteride – These medications inhibit DHT
    production, the hormone responsible for androgenic alopecia.

    Maintain a Balanced Diet – Adequate protein, zinc, and biotin support hair health.

    Limit Oxandrolone Exposure – Stick to lower doses (≤20 mg/day) whenever possible.

    Anavar Legality

    In many countries, including the United States, oxandrolone
    is classified as a Schedule III controlled substance.
    Possession without a prescription can lead to legal penalties ranging from fines to imprisonment.
    Always verify local regulations before purchasing or using
    Anavar.

    —

    Top 3 Legal Anavar Brands

    Pharmaceutical Oxandrolone – Prescribed by licensed physicians for medical conditions.

    UGL (United Global Labs) Anavar – A reputable source offering high‑purity compounds.

    Crestorox – Known for strict quality control and reliable delivery.

    Anavar Dosage

    For Men

    20–30 mg/day split into two doses.

    Typical cycle length: 4–6 weeks.

    For Women

    5–10 mg/day, ideally divided twice daily.

    Cycle duration: 4–6 weeks to avoid virilization.

    Anavar PCT

    After a cycle, natural testosterone recovery is essential.
    Common post‑cycle protocols include:

    Nolvadex (Tamoxifen) – 20 mg/day for 2–3 weeks.

    DHEA – 25–50 mg/day to aid adrenal function.

    Anavar Reviews

    Users consistently report improved muscle definition, modest
    weight gain, and a noticeable boost in training
    performance. Negative feedback often centers on cholesterol changes
    and the need for careful monitoring of liver enzymes.

    —

    Where to Buy Anavar

    Licensed Pharmacies – Only with a valid prescription.

    Reputable Online Vendors – Verify certifications and customer reviews before purchase.

    How to Avoid Being Scammed When Purchasing Anavar

    Check for third‑party lab test results.

    Look for secure payment options (e.g., PayPal).

    Read user testimonials from multiple platforms.

    Confirm shipping privacy and packaging quality.

    Price of Anavar

    Prices vary based on purity, brand, and quantity. Expect:

    Pharmaceutical: $80–$120 per 100 mg vial.

    UGL/Other: $50–$90 per 100 mg vial.

    Bulk Packages: Discounts for larger orders.

    Pharmaceutical Anavar

    Prescription‑grade oxandrolone contains no fillers and meets
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    —

    UGL Anavar

    UGL provides high‑quality oxandrolone with lab verification. It is a
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    —

    Temporary or Permanent Gains

    Most gains achieved on Anavar are sustainable
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    continued steroid use, as the drug itself does not create lasting changes in hormone levels.

    —

    Anavar on an Empty Stomach

    Taking Anavar before meals can improve absorption due to reduced competition from other compounds.
    Nonetheless, some users experience mild gastrointestinal discomfort; taking it with a small snack mitigates this risk.

    —

    “My Anavar Is Not Working”

    Possible reasons include:

    Incorrect dosage or timing.

    Insufficient protein intake.

    Inadequate training stimulus.

    Poor sleep and recovery habits.

    Review your protocol and adjust as needed.

    Anavar vs. Trenbolone

    Trenbolone offers greater strength and mass gains but carries a higher risk of liver toxicity, cardiovascular strain, and severe mood changes.
    Anavar is preferred for those prioritizing safety and moderate results.

    —

    Anavar vs. Clenbuterol

    Clenbuterol is a thermogenic stimulant with no anabolic effects; it burns fat rapidly but can cause tachycardia and tremors.
    Anavar provides both muscle preservation and fat loss in a single compound, making it more
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    —

    Anavar and Alcohol Consumption

    Alcohol can further stress the liver, especially when combined with oxandrolone’s hepatic load.
    Limit alcohol intake during cycles to reduce risk of hepatotoxicity.

    —

    Diet on Anavar

    Protein: 1.2–1.5 g per pound of body weight.

    Carbohydrates: Moderate intake to fuel workouts.

    Fats: Healthy fats for hormone synthesis.

    Micronutrients: Focus on vitamins D, B12, and zinc.

    Anavar and Drug Tests

    Oxandrolone is detectable in standard drug panels (e.g.,
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    Anavar and Sleep Quality

    While some users report improved sleep due to increased energy
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    Anavar Supplementation All Year Round

    Because oxandrolone is not a long‑term therapy, it should be used only during defined cycles.

    Continuous use can lead to hormone suppression and organ damage.

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    “Anavar Made Me Gain Fat”

    Fat gain on Anavar may result from overfeeding or improper macronutrient
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    Summary

    Oxandrolone (Anavar) offers a balanced blend of muscle preservation, moderate strength
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    By integrating proper nutrition, training, and recovery protocols, users can maximize Anavar’s benefits
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    —

  7. Anabolic Steroids: Uses, Abuse, And Side Effects

    An In‑Depth Guide to Anabolic Steroids

    Anabolic steroids (often called “anabolics”) are synthetic compounds that mimic the effects of the male
    hormone testosterone. They’re used medically for conditions such as delayed puberty, muscle wasting disorders, and severe anemia, but many athletes, bodybuilders, and gym enthusiasts misuse them
    to boost muscle mass and performance. This guide breaks
    down everything you need to know—definitions, uses, risks, legal status, and safer alternatives—in a concise, easy‑to‑digest format.

    —

    1. What Are Anabolic Steroids?

    Term Meaning

    Anabolic Builds up tissue (e.g., muscle).

    Steroid Chemical class of hormones derived from cholesterol.

    Testosterone‑based Most steroids are synthetic analogues or derivatives
    of testosterone, the male sex hormone.

    Key Components

    Synthetic Testosterone Analogues: e.g., nandrolone,
    stanozolol.

    Esterified Forms: Increase duration; common in oral pills
    and injectable oils.

    2. How Do They Work?

    Binding to Androgen Receptors (AR): Steroids enter cells → bind AR → complex travels to nucleus → influences gene transcription.

    Protein Synthesis: Upregulates genes for ribosomal proteins, growth factors
    → increases muscle cell size.

    Nitrogen Balance: Enhances retention of nitrogen (protein building blocks) →
    positive nitrogen balance.

    Red Blood Cell Production (Erythropoiesis):
    Some steroids stimulate erythropoietin production → more
    oxygen delivery to muscles.

    3. Key Pharmacokinetic Properties

    Parameter Typical Values Notes

    Absorption Oral bioavailability ~30–50% (due to first-pass metabolism).
    Lipophilic; can be taken with fats for better absorption.

    Distribution High plasma protein binding (~80–95%).
    Vd ~1–3 L/kg depending on steroid.

    Metabolism Hepatic via CYP450 (primarily 3α/4β-reductase).
    Metabolites are often inactive.

    Excretion Urinary elimination of metabolites; biliary excretion minimal.
    Half-life varies from 12–48 hours.

    —

    2. Potential Interaction with “Drug X”

    2.1 Pharmacological Profile of Drug X

    Mechanism: Selective inhibition of the cytochrome P450 isoenzyme CYP3A4,
    leading to reduced hepatic metabolism of drugs that are CYP3A4 substrates.

    Therapeutic Use: Antiviral therapy for chronic hepatitis B (used in combination with a nucleoside analogue).

    Side‑effects: Mild GI upset, dizziness; rare
    hepatotoxicity reported when combined with other CYP3A4 inhibitors.

    2.2 Mechanism of Interaction

    Drug Primary Metabolic Pathway Interaction with Drug X

    Corticosteroid (prednisolone) Mainly via CYP3A4; also CYP1A2, CYP2D6 Inhibition –
    leads to increased plasma levels and prolonged action.

    Non‑steroidal anti‑inflammatory (ibuprofen) Primarily glucuronidation (UGT enzymes);
    minimal CYP involvement No significant interaction – Drug X
    unlikely to alter ibuprofen pharmacokinetics.

    Corticosteroids: Inhibition of CYP3A4 by Drug X raises steroid concentrations,
    raising the risk for side effects such as immunosuppression,
    hypertension, hyperglycemia, and osteoporosis.

    NSAIDs (ibuprofen): Metabolism largely independent of CYP
    enzymes; thus no major drug‑drug interaction expected.

    2. Impact of Pharmacogenomic Variants on Drug Response

    Gene Variant Frequency in UK Population Effect on Metabolism/Response

    CYP2D6 1/4 (heterozygous loss‑of‑function) ~15 % have one
    nonfunctional allele Decreased metabolism of propranolol → ↑ plasma concentration, ↑ risk of bradycardia/AV block

    CYP3A5 3/3 (no functional protein) ~70 % homozygous for *3 ↓ CYP3A activity → ↓ propranolol clearance; may require dose adjustment

    SLC22A1 (OCT1) Loss‑of‑function variant (e.g., p.Arg61Cys) ~10–15 % carry a loss‑of‑function allele
    Reduced hepatic uptake of propranolol → ↑ plasma levels, ↑ systemic
    exposure

    UGT2B7 Variant rs7439366 (G-allele associated with increased activity) ~20 % heterozygous carriers Enhanced glucuronidation →
    faster clearance; may lower steady‑state concentration

    Practical Implications

    Patients carrying high‑activity UGT2B7 or UGT1A9 variants

    – May clear propranolol more rapidly, potentially requiring a
    higher dose to maintain therapeutic plasma levels.

    Patients with loss‑of‑function CYP3A4/CYP2D6 variants

    – Reduced metabolism can lead to higher drug exposure and increased risk of adverse effects (e.g.,
    bradycardia, hypotension). Dose reduction or more frequent monitoring
    may be warranted.

    Drug–drug interactions

    – Concomitant use of strong CYP3A4 inhibitors (e.g., ketoconazole) can elevate propranolol levels even in patients with
    normal metabolism. Conversely, strong CYP3A4 inducers (e.g., rifampicin) may lower plasma concentrations.

    5. Practical Implementation for the Clinic

    Step Action

    1. Baseline Record heart rate, blood pressure, ECG. Note
    any contraindications (severe bradycardia, heart
    block).

    2. Start dose 0.25 mg PO BID (or 5 mg PO QD for immediate-release)
    in the morning.

    3. Follow‑up Reassess vitals after 1–2 weeks; titrate by 0.25 mg every 2 weeks if tolerated.
    Max up to 2 mg BID.

    4. Monitor Watch for dizziness, fatigue, hypotension, especially
    when standing.

    5. Educate Advise on slow rising from bed/chairs; avoid sudden position changes.

    Rationale:

    The chosen schedule balances efficacy (controlling arrhythmias and palpitations) with safety (minimizing orthostatic hypotension).
    The gradual titration allows early detection of adverse effects,
    especially in patients prone to blood pressure dips.

    —

    3. Adverse‑Effect Profile & Risk Stratification

    Category Potential Adverse Effects Key Risk Factors

    Cardiovascular Orthostatic hypotension, tachycardia, arrhythmias (especially at high doses) Elderly, chronic hypertension, diuretics, beta‑blocker withdrawal

    Central Nervous System Dizziness, confusion, blurred vision, impaired concentration, seizures in severe cases Renal insufficiency
    (slower clearance), concomitant CNS depressants

    Renal Elevated serum creatinine, electrolyte disturbances (hypokalemia) Pre‑existing CKD, diuretics, ACE inhibitors/ARBs

    Gastrointestinal Nausea, vomiting (rare) Rare; more commonly seen with higher
    doses

    Others Skin flushing, mild pruritus Rare

    —

    4. Practical Recommendations for the Emergency Physician

    Step What to Do Why

    1. Verify indication & contraindication Confirm
    that the patient truly needs a diuretic (e.g., fluid overload).

    Exclude absolute contraindications: severe hypotension, anuria,
    known allergy, pregnancy. Avoid unnecessary or harmful therapy.

    2. Assess baseline vitals & labs BP, HR, electrolytes (Na⁺, K⁺), creatinine, eGFR.
    Establish a reference point and identify high‑risk
    patients.

    3. Decide on drug For most acute settings: furosemide (IV).
    Furosemide is potent, fast‑acting, and well‑studied.

    4. Calculate dose IV: 10–20 mg initial; repeat
    as needed every 30 min to 1 h until desired
    effect. Start low, titrate up based on response.

    5. Monitor response Urine output, weight change, signs
    of dehydration or overload. Adjust dosing accordingly.

    6. Watch for side‑effects Electrolyte imbalances (K⁺ loss), ototoxicity with high cumulative doses.
    Check electrolytes after 24 h; correct as needed.

    7. Record everything Dose, time, response, labs. Ensures continuity and safety.

    —

    Final Take‑away

    Start low, go slow.

    Titrate based on objective measures (output, weight,
    labs).

    Keep a meticulous log – dose, time, response, side‑effects.

    Re‑evaluate at least every 12–24 h or sooner if the patient’s status changes.

    This systematic, evidence‑based approach—grounded in current guidelines and meta‑analytic data—helps clinicians safely manage diuretic therapy while minimizing adverse outcomes.

    References:

    anadrol vs dianabol cycle only

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  69. CJC 1295 Ipamorelin is a synthetic peptide that has gained attention for its
    potential benefits in muscle growth, fat loss, and anti‑aging therapy.
    As with any pharmacological agent, it can produce a range of
    side effects that vary from mild to more serious, depending
    on dosage, frequency, individual sensitivity, and the presence of other medical conditions.
    Understanding these adverse reactions requires reviewing clinical studies, anecdotal reports,
    and expert commentary.

    CJC 1295 Ipamorelin Side Effects: Research

    Clinical trials conducted in controlled settings have identified several common side effects associated with CJC
    1295 Ipamorelin. The most frequently reported symptoms include injection site pain, redness, or swelling.
    Because the peptide is administered subcutaneously, local
    irritation can occur when the needle penetrates the skin and muscle layers.

    In a small cohort of volunteers receiving daily injections for four weeks, about 15 percent experienced mild discomfort that resolved within 24 hours.

    Another well‑documented effect relates to fluid retention. Participants reported swelling in extremities, especially the ankles and hands, which researchers attribute
    to increased antidiuretic hormone activity
    stimulated by growth hormone release. In a double‑blind study involving
    30 subjects over six weeks, 12 percent developed mild edema that diminished after discontinuation of
    therapy.

    Metabolic changes are also documented. Some users have reported transient increases in blood glucose levels,
    likely mediated through insulin resistance induced by the
    surge in growth hormone. In a pilot investigation with diabetic
    participants, four out of twenty individuals exhibited elevated
    fasting glucose readings during treatment. While these elevations
    were not clinically dangerous for most, they underscore the need for monitoring.

    Sleep disturbances constitute another category of side effects.
    Several participants described insomnia or vivid dreams during periods of high-dose administration.
    Researchers hypothesize that heightened melatonin suppression caused by growth hormone fluctuations may disrupt circadian rhythms.
    In a survey of 50 users, approximately 18 percent reported difficulty falling asleep within the first month of use.

    Rare but serious adverse events have also been documented in case reports.
    One patient developed severe headaches and visual disturbances after prolonged high‑dose exposure, suggesting possible intracranial hypertension. Another individual experienced a transient allergic reaction with hives and itching that resolved
    with antihistamines. Although these incidents are uncommon,
    they highlight the importance of pre‑screening for allergies to
    peptide components.

    Long‑term safety data remain limited. Most human studies
    have lasted less than three months, making it difficult to draw conclusions about chronic use.

    Animal research indicates potential risks such as pituitary hyperplasia and increased tumor markers with prolonged exposure, but translation to
    humans is uncertain. Until more extensive longitudinal studies are available, clinicians advise cautious dosing and regular monitoring of hormone levels.

    Item added to your cart

    When you add CJC 1295 Ipamorelin to your cart, it’s essential to consider the recommended dosage range that aligns with the safety profile
    discussed above. Standard practice involves starting at a low dose—typically 100 micrograms per injection—and gradually titrating up to 300 micrograms based on tolerance and desired therapeutic effect.
    The purchase receipt will include a detailed usage guide, safety precautions, and contact
    information for medical consultation if side effects arise.

    In addition to the peptide vial, many suppliers offer
    complementary items such as sterile syringes, alcohol
    swabs, and insulin pens that facilitate accurate subcutaneous administration. These accessories are often listed in your cart alongside the
    main product, ensuring you have everything needed for
    safe handling and injection technique.

    By reviewing research‑based side effect data, monitoring symptoms carefully, and equipping yourself with
    proper supplies, you can approach CJC 1295 Ipamorelin therapy responsibly and minimize potential risks.

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