Lecture 7 EAs Flashcards

(65 cards)

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3
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Chromium – LO6a Structure & Synthesis

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Trace mineral; biologically active as trivalent chromium (Cr III), found bound to transferrin and a low–molecular weight chromium-binding substance; not synthesized by the body.

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4
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Chromium – LO6b Sources & Normal Function (non‑EA, non‑sport)

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Food sources include brewer’s yeast, broccoli, whole grains, nuts, liver, prunes, egg yolks and some fruits/vegetables. In the body Cr III acts as a cofactor that potentiates insulin action, helping carbohydrate, lipid and protein metabolism.

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5
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Chromium – LO6c ‘Safe’ Rate of Intake (non‑EA, non‑sport)

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Adequate Intake (AI) is about 35 μg/day for adult men and 25 μg/day for adult women; no formal UL has been set, but typical intakes are in the tens of micrograms per day.

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6
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Chromium – LO6d Drug Test Value in Sport

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Chromium is not on the WADA Prohibited List, not tracked in the Athlete Biological Passport, and is permitted for athletes.

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7
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Chromium – LO6e EA Intake & Risks in Sport Settings

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Common supplement doses are 200–600 μg/day as chromium picolinate. High chronic intakes may interfere with iron and zinc metabolism and, in cell culture, very high doses have been linked to chromosomal damage; long‑term safety of large supplemental doses is uncertain.

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8
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Chromium – LO6f Rationale & Purported Mechanism in Sport

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Because chromium potentiates insulin, it is marketed to improve glucose uptake, enhance protein synthesis and favor loss of fat mass with gain in lean mass, particularly for resistance/power athletes. However the exact ergogenic mechanism is unclear.

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9
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Chromium – LO6g Research Evidence

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Controlled training studies generally show no significant benefits of chromium supplementation on muscle mass, strength or performance compared with placebo; evidence does not support a meaningful ergogenic effect.

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10
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Coenzyme Q10 – LO6a Structure & Synthesis

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CoQ10 (ubiquinone/ubiquinol) is a lipid‑soluble, vitamin‑like benzoquinone with a long isoprenoid side chain; synthesized endogenously from acetyl‑CoA via the mevalonate pathway.

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11
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Coenzyme Q10 – LO6b Sources & Normal Function

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Found mainly in meats, fish, nuts and some oils, and in supplements. In tissues, especially heart muscle, it is an electron carrier in the mitochondrial electron transport chain and also acts as an antioxidant.

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12
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Coenzyme Q10 – LO6c ‘Safe’ Intake (non‑sport)

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Intakes up to about 1200 mg/day in adults have been reported as well tolerated in clinical studies; no official RDA or UL is set.

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13
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Coenzyme Q10 – LO6d Drug Test Value in Sport

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CoQ10 is not on the WADA Prohibited List and is not monitored by the ABP; it is allowed for use by athletes.

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14
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Coenzyme Q10 – LO6e EA Intake & Risks in Sport Settings

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Typical EA doses are 60–200 mg/day for several weeks. Side‑effects are usually mild (GI upset, nausea); some studies report higher plasma creatine kinase or markers of oxidative stress during intense exercise, so high‑dose use may not be harmless.

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15
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Coenzyme Q10 – LO6f Rationale & Purported Mechanism in Sport

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Because CoQ10 participates in electron transport and oxidative phosphorylation, supplements are marketed to enhance mitochondrial ATP production, improve stamina and support cardiovascular function in endurance and high‑intensity aerobic exercise.

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16
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Coenzyme Q10 – LO6g Research Evidence

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Most studies show increased plasma or muscle CoQ10 but no clear improvements in VO2max, time‑to‑exhaustion, or cycling/running performance; effects on oxidative stress markers are inconsistent. Overall evidence for performance benefits is weak.

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17
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Ribose – LO6a Structure & Synthesis

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D‑ribose is a five‑carbon (pentose) sugar; endogenously synthesized via the pentose phosphate pathway and incorporated into ATP, RNA and other nucleotides.

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18
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Ribose – LO6b Sources & Normal Function

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Small amounts are present in some fruits and vegetables; most body ribose is produced endogenously. It provides the ribose backbone for ATP and nucleic acids, important for cellular energy and genetic material.

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19
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Ribose – LO6c ‘Safe’ Intake (non‑sport)

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No RDA is set. Supplemental intakes around 10–20 g/day are commonly used in studies; higher acute doses can cause GI discomfort.

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20
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Ribose – LO6d Drug Test Value in Sport

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Ribose is not on the WADA Prohibited List and is not monitored; it is a permitted nutritional supplement.

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21
Q

Ribose – LO6e EA Intake & Risks in Sport Settings

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EA protocols often use ~4 g ribose, four times per day (≈16 g/day) for several days. Main side‑effects are diarrhea, nausea and headaches at higher intakes; no major systemic toxicities reported in healthy people.

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22
Q

Ribose – LO6f Rationale & Purported Mechanism in Sport

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Because ATP resynthesis depends on ribose for adenine nucleotides, ribose is marketed to speed recovery of muscle ATP after intense bouts and to enhance short‑term explosive or repeated high‑intensity efforts (resistance/power and sprint exercise).

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23
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Ribose – LO6g Research Evidence

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Controlled trials generally show that ribose supplementation does not significantly improve ATP recovery or power output during repeated high‑intensity exercise compared with placebo; evidence does not support a strong ergogenic effect.

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24
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Inosine – LO6a Structure & Synthesis

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Inosine is a purine nucleoside formed from hypoxanthine and ribose; produced endogenously as an intermediate in purine metabolism.

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25
Inosine – LO6b Sources & Normal Function
Found in small amounts in organ meats and brewer’s yeast. In cells it is involved in nucleotide metabolism and can be converted into ATP precursors or incorporated into tRNA.
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Inosine – LO6c ‘Safe’ Intake (non‑sport)
No RDA established. Supplemental intakes of several grams per day have been used short‑term in studies; long‑term high doses are not considered safe due to uric acid production.
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Inosine – LO6d Drug Test Value in Sport
Inosine is not listed as a prohibited substance by WADA and is not monitored by the ABP.
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Inosine – LO6e EA Intake & Risks in Sport Settings
EA doses around 5–6 g/day have been used. Inosine metabolism increases serum uric acid and can promote uric‑acid crystal deposition, increasing risk of gout and kidney stones; this is the main safety concern.
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Inosine – LO6f Rationale & Purported Mechanism in Sport
Inosine is marketed to increase ATP availability and 2,3‑DPG in red blood cells to facilitate O2 unloading, and to act as a cardiac vasodilator, potentially supporting both anaerobic and aerobic performance.
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Inosine – LO6g Research Evidence
Studies in competitive cyclists and other athletes show no significant improvement in aerobic cycling performance or anaerobic Wingate test outcomes versus placebo; evidence does not support an ergogenic effect.
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Choline – LO6a Structure & Synthesis
Choline is a water‑soluble quaternary amine; synthesized in liver and kidney from serine and methionine and also obtained preformed in the diet.
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Choline – LO6b Sources & Normal Function
Rich food sources include egg yolks, liver, meat, soybeans, wheat germ and some vegetables. Choline is a component of phosphatidylcholine in cell membranes and lipoproteins, is required for VLDL export from liver, and is a precursor to the neurotransmitter acetylcholine.
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Choline – LO6c ‘Safe’ Intake (non‑sport)
AI for adults is ~550 mg/day for men and 425 mg/day for women; the Tolerable Upper Intake Level is about 3.5 g/day due to risk of hypotension and fishy body odor at high doses.
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Choline – LO6d Drug Test Value in Sport
Choline is not prohibited by WADA and is not part of the Athlete Biological Passport; it is permitted.
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Choline – LO6e EA Intake & Risks in Sport Settings
EA doses of 3–7.5 g/day have been used. High intakes can cause hypotension, excessive sweating, diarrhea and a strong fishy body odor due to trimethylamine accumulation, especially in people with trimethylaminuria.
36
Choline – LO6f Rationale & Purported Mechanism in Sport
Because choline is a precursor for acetylcholine at the neuromuscular junction, supplements are marketed to maintain ACh synthesis during prolonged exercise and to support nerve–muscle transmission and “fat burning,” especially for resistance/power athletes and bodybuilders.
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Choline – LO6g Research Evidence
In soldiers performing prolonged loaded walking and in endurance exercise studies, choline supplementation greatly raised plasma choline but did not improve time to exhaustion, VO2, heart rate, RPE or performance vs placebo; evidence does not support an ergogenic effect.
38
Hydroxycitrate (HCA) – LO6a Structure & Synthesis
Hydroxycitrate is a derivative of citric acid found naturally in the rind of Garcinia cambogia and some other tropical plants; it is extracted and standardized for use in supplements.
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Hydroxycitrate (HCA) – LO6b Sources & Normal Function
In food it is present mainly in Garcinia fruit used in some Asian cuisines. It inhibits ATP‑citrate lyase, an enzyme linking carbohydrate metabolism to fatty‑acid synthesis; otherwise it has no essential nutrient role.
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Hydroxycitrate (HCA) – LO6c ‘Safe’ Intake (non‑sport)
There is no established RDA. Commercial weight‑loss products typically provide about 1500 mg/day HCA (e.g., 500 mg three times daily), which has been used for weeks in trials without major acute toxicity in most participants.
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Hydroxycitrate (HCA) – LO6d Drug Test Value in Sport
HCA is not on the WADA Prohibited List and is not monitored in the ABP.
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Hydroxycitrate (HCA) – LO6e EA Intake & Risks in Sport Settings
Similar doses to weight‑loss studies (≈1.5–3 g/day) are used. Reported side‑effects include GI discomfort; some animal work suggests potential testicular toxicity, and rare case reports have raised liver safety questions for certain herbal mixtures.
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Hydroxycitrate (HCA) – LO6f Rationale & Purported Mechanism in Sport
By inhibiting ATP‑citrate lyase, HCA is proposed to reduce de novo lipogenesis, increase fat oxidation and glycogen storage, and thereby promote weight loss and endurance by sparing glycogen during prolonged exercise.
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Hydroxycitrate (HCA) – LO6g Research Evidence
Human studies generally show no meaningful difference in weight loss, fat mass loss, respiratory quotient, or energy expenditure vs placebo in obese individuals or during submaximal exercise; current evidence does not support HCA as an effective ergogenic or weight‑loss aid.
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Glycerol – LO6a Structure & Synthesis
Glycerol is a three‑carbon sugar alcohol forming the backbone of triacylglycerols and phospholipids; it is produced endogenously during lipolysis and can be converted to glycolytic intermediates in the liver.
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Glycerol – LO6b Sources & Normal Function
Occurs in dietary fats and is also used as a food additive and pharmaceutical solvent. In metabolism, glycerol can be used for gluconeogenesis and as an energy substrate; it is also osmotically active and can influence fluid distribution between compartments.
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Glycerol – LO6c ‘Safe’ Intake (non‑sport)
Single doses up to about 1.2 g/kg body mass with 1–2 L of water have been used to induce hyperhydration in healthy adults; glycerol has low acute toxicity, though very high doses can cause nausea or headache.
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Glycerol – LO6d Drug Test Value in Sport
Glycerol used to be prohibited as a plasma‑expanding agent but was removed from the WADA Prohibited List in 2018; it is currently permitted and not tracked by the ABP.
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Glycerol – LO6e EA Intake & Risks in Sport Settings
EA protocols use ~1.0–1.2 g/kg body mass glycerol in 1–2 L of water ingested before exercise. Side‑effects can include nausea, bloating, light‑headedness and dizziness; however, toxicity is generally low.
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Glycerol – LO6f Rationale & Purported Mechanism in Sport
Pre‑exercise glycerol plus water increases total body water and plasma volume by promoting renal water retention and osmotic fluid shifts, producing ‘hyperhydration’ that may reduce cardiovascular and thermal strain during prolonged exercise in the heat (endurance aerobic events).
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Glycerol – LO6g Research Evidence
Studies show that glycerol plus water can increase fluid retention for several hours and, in some trials, prolong time‑to‑exhaustion during steady‑state cycling in the heat compared with water alone; evidence suggests a modest ergogenic effect for hot‑environment endurance.
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Medium‑Chain Triglycerides (MCT) – LO6a Structure & Synthesis
MCTs are triacylglycerols containing medium‑chain fatty acids (typically 8–12 carbons). They occur naturally in coconut and palm kernel oil and can be isolated and refined as supplements.
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Medium‑Chain Triglycerides (MCT) – LO6b Sources & Normal Function
Food sources include coconut oil and some full‑fat dairy; supplemental MCT oil is widely sold. MCTs are rapidly absorbed, transported via the portal vein and oxidized in the liver, providing a quick energy source and alternative fuel.
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Medium‑Chain Triglycerides (MCT) – LO6c ‘Safe’ Intake (non‑sport)
Within a normal fat intake (~30% of energy), single doses up to ~30 g of MCT at once are considered the upper limit before GI side‑effects become common.
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Medium‑Chain Triglycerides (MCT) – LO6d Drug Test Value in Sport
MCTs are a permitted dietary fat source and are not on the WADA Prohibited List or ABP.
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Medium‑Chain Triglycerides (MCT) – LO6e EA Intake & Risks in Sport Settings
EA protocols often combine 25–30 g MCT with carbohydrate before or during prolonged exercise. Side‑effects frequently include GI cramping and diarrhea, which can impair performance.
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Medium‑Chain Triglycerides (MCT) – LO6f Rationale & Purported Mechanism in Sport
MCTs are marketed as a rapidly oxidizable fat that bypasses carnitine‑dependent transport into mitochondria, potentially sparing muscle and liver glycogen and serving as an extra fuel during long‑duration aerobic exercise.
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Medium‑Chain Triglycerides (MCT) – LO6g Research Evidence
Research is mixed: some studies show small performance benefits when MCT is combined with carbohydrate, but many show no improvement or even impaired performance due to GI distress. Overall, evidence does not strongly support MCTs as a reliable ergogenic aid.
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Carbohydrate Loading – LO6a Structure & Synthesis
The relevant ‘structure’ is muscle and liver glycogen, a highly branched polymer of glucose synthesized endogenously from dietary carbohydrate via glycogenesis.
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Carbohydrate Loading – LO6b Sources & Normal Function
Carbohydrate comes from foods such as grains, pasta, bread, rice, fruits and sugars. Glycogen is the main storage form of carbohydrate and a critical fuel for moderate‑to‑high‑intensity exercise and for CNS function via blood glucose.
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Carbohydrate Loading – LO6c ‘Safe’ Intake (non‑sport)
For active adults, 45–65% of total energy from carbohydrate (about 5–7 g/kg/day) is generally recommended; high‑carbohydrate diets used for loading (8–12 g/kg/day for a day or more) are considered safe for healthy individuals.
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Carbohydrate Loading – LO6d Drug Test Value in Sport
High‑carbohydrate intake and elevated muscle glycogen are not prohibited by WADA and are not tracked in the ABP; CHO loading is a permitted nutrition strategy.
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Carbohydrate Loading – LO6e EA Intake & Risks in Sport Settings
Classic loading protocols combine prior glycogen‑depleting exercise with several days of very high carbohydrate intake (e.g., 8–12 g/kg/day). Side‑effects may include GI discomfort, a feeling of “heaviness,” and acute weight gain because each gram of glycogen stores ~2.7 g of water.
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Carbohydrate Loading – LO6f Rationale & Purported Mechanism in Sport
By supercompensating muscle glycogen, CHO loading increases the amount of stored carbohydrate available for oxidation during endurance events, delaying glycogen depletion and fatigue and extending time‑to‑exhaustion in prolonged whole‑body endurance aerobic exercise (>60 min).
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Carbohydrate Loading – LO6g Research Evidence
Well‑designed studies show that CHO loading can approximately double muscle glycogen content in the exercised muscles and significantly prolong time‑to‑exhaustion in events lasting >60–90 minutes; it is one of the most consistently supported nutritional ergogenic strategies.