Summer Shred Stack

Summer Shred Stack

Summer Shred Stack

Get beach-ready with our Summer Shred Stack, crafted to enhance fat burning and muscle definition. Perfect for achieving a lean, sculpted physique, this stack boosts metabolism and preserves muscle mass. Make a statement this summer with our specialized stack for a lean, beach-perfect body
Regular price $259.85 Sale price $220.87
/
  • In stock
  • Inventory on the way
  • 100% MONEY BACK
  • FREE SHIPPING
  • MADE IN FDA INSPECTED FACILITY

BURN FAT, MAXIMISE MUSCLE GROWTH , GET SHREDDED

How to use Summer Shred Stack to help you get the ultimate body?

Fat Reducer

As a dietary supplement, take 1-2 capsules per day. For Enhanced results, take ECA Shred 30 before pre-cardio exercises


Carb to Muscle Converter

Take 4 capsules 1-2x daily with your highest carb meals to effectively partition carbohydrates into the muscle and away from fat storage.


Belly Fat Destroyer

As a dietary supplemets, take 4 capsules daily. For Enhanced result, take Code Red first thing in the morning.


SCIENTIFIC STUDIES INFO

A high-protein diet induces sustained reductions in appetite, ad libitum caloric intake, and body weight despite compensatory changes in diurnal plasma leptin and ghrelin concentrations

Background: Ad libitum, low-carbohydrate diets decrease caloric intake and cause weight loss. It is unclear whether these effects are due to the reduced carbohydrate content of such diets or to their associated increase in protein intake.

Objective: We tested the hypothesis that increasing the protein content while maintaining the carbohydrate content of the diet lowers body weight by decreasing appetite and spontaneous caloric intake.

Design: Appetite, caloric intake, body weight, and fat mass were measured in 19 subjects placed sequentially on the following diets: a weight-maintaining diet (15% protein, 35% fat, and 50% carbohydrate) for 2 wk, an isocaloric diet (30% protein, 20% fat, and 50% carbohydrate) for 2 wk, and an ad libitum diet (30% protein, 20% fat, and 50% carbohydrate) for 12 wk. Blood was sampled frequently at the end of each diet phase to measure the area under the plasma concentration versus time curve (AUC) for insulin, leptin, and ghrelin.

Results: Satiety was markedly increased with the isocaloric high-protein diet despite an unchanged leptin AUC. Mean (+/-SE) spontaneous energy intake decreased by 441 +/- 63 kcal/d, body weight decreased by 4.9 +/- 0.5 kg, and fat mass decreased by 3.7 +/- 0.4 kg with the ad libitum, high-protein diet, despite a significantly decreased leptin AUC and increased ghrelin AUC.

Conclusions: An increase in dietary protein from 15% to 30% of energy at a constant carbohydrate intake produces a sustained decrease in ad libitum caloric intake that may be mediated by increased central nervous system leptin sensitivity and results in significant weight loss. This anorexic effect of protein may contribute to the weight loss produced by low-carbohydrate diets.

Fat burners: nutrition supplements that increase fat metabolism

The term ‘fat burner’ is used to describe nutrition supplements that are claimed to acutely increase fat metabolism or energy expenditure, impair fat absorption, increase weight loss, increase fat oxidation during exercise, or somehow cause long-term adaptations that promote fat metabolism. Often, these supplements contain a number of ingredients, each with its own proposed mechanism of action and it is often claimed that the combination of these substances will have additive effects. The list of supplements that are claimed to increase or improve fat metabolism is long; the most popular supplements include caffeine, carnitine, green tea, conjugated linoleic acid, forskolin, chromium, kelp and fucoxanthin. In this review the evidence for some of these supplements is briefly summarized. Based on the available literature, caffeine and green tea have data to back up its fat metabolism-enhancing properties. For many other supplements, although some show some promise, evidence is lacking. The list of supplements is industry-driven and is likely to grow at a rate that is not matched by a similar increase in scientific underpinning.

Comparison of alternative primary outcome measures for use in lupus nephritis clinical trials

 

Objective: Clinical trials of therapies for lupus nephritis have used many different primary outcome measures, ranging from complete response to time to end-stage renal disease. The objective of this study was to compare several possible outcome measures, using data from a large, multicenter trial of abatacept in lupus nephritis, to gain insight into which outcome measure, if any, was best able to discern differences among treatment groups.

Methods: Study patients received either abatacept or placebo, on a background of mycophenolate mofetil and glucocorticoids. Using data from this trial, the following primary outcome measures at 24 and 52 weeks were compared: complete response rate, major clinical response rate, total response rate (complete plus partial response), improvement in proteinuria, improvement in estimated glomerular filtration rate, and frequency of treatment failure. Time to complete response was also evaluated.

Results: Complete response rate, major clinical response rate, and time to complete response were the measures that best discriminated between the abatacept groups and placebo, and the sensitivities of these 3 measures were comparable. For these measures, sample sizes of 50 patients would have been sufficient to demonstrate a statistically significant difference between treatment and control at 52 weeks. Each of the other measures also discriminated between treatment and control, but much larger group sizes would have been required to determine statistical significance.

Conclusion: The choice of primary outcome measure can substantially influence the ability to detect therapeutic benefit in lupus nephritis trials. This study suggests that complete response rate, major clinical response rate at 52 weeks, and time to complete response may be the most sensitive outcome measures for detecting differences among therapeutic regimens.

Trial registration: ClinicalTrials.gov NCT00430677.

The effects of red bull energy drink on human performance and mood
Background:

The effects of Red Bull Energy Drink, which includes taurine, glucuronolactone, and caffeine amongst the ingredients, were examined over 3 studies in a total of 36 volunteers. Assessments included psychomotor performance (reaction time, concentration, memory), subjective alertness and physical endurance. When compared with control drinks, Red Bull Energy Drink significantly (P < 0.05) improved aerobic endurance (maintaining 65-75% max. heart rate) and anaerobic performance (maintaining max. speed) on cycle ergometers. Significant improvements in mental performance included choice reaction time, concentration (number cancellation) and memory (immediate recall), which reflected increased subjective alertness. These consistent and wide ranging improvements in performance are interpreted as reflecting the effects of the combination of ingredients.

Intestinal Epithelial Cell Tyrosine Kinase 2 Transduces IL-22 Signals To Protect from Acute Colitis
Background:

In the intestinal tract, IL-22 activates STAT3 to promote intestinal epithelial cell (IEC) homeostasis and tissue healing. The mechanism has remained obscure, but we demonstrate that IL-22 acts via tyrosine kinase 2 (Tyk2), a member of the Jak family. Using a mouse model for colitis, we show that Tyk2 deficiency is associated with an altered composition of the gut microbiota and exacerbates inflammatory bowel disease. Colitic Tyk2(-/-) mice have less p-STAT3 in colon tissue and their IECs proliferate less efficiently. Tyk2-deficient primary IECs show reduced p-STAT3 in response to IL-22 stimulation, and expression of IL-22-STAT3 target genes is reduced in IECs from healthy and colitic Tyk2(-/-) mice. Experiments with conditional Tyk2(-/-) mice reveal that IEC-specific depletion of Tyk2 aggravates colitis. Disease symptoms can be alleviated by administering high doses of rIL-22-Fc, indicating that Tyk2 deficiency can be rescued via the IL-22 receptor complex. The pivotal function of Tyk2 in IL-22-dependent colitis was confirmed in Citrobacter rodentium-induced disease. Thus, Tyk2 protects against acute colitis in part by amplifying inflammation-induced epithelial IL-22 signaling to STAT3.

*Summer Shred Stack Promotion Terms and Conditions

  1. 1 Promotion Overview: The Summer Shred Stack promotion offers participants the chance to receive a complimentary tub of All Day Shred with their purchase. Every third order of the Summer Shred Stack will be selected for this gift.

  1. 2 Eligibility: This promotion is open to customers who are legal residents of Australia, New Zealand or Singapore and are of 16 years of age or older. Employees of Enhanced Australasia, its affiliates, subsidiaries, advertising, and promotion agencies, and suppliers, (collectively the “Employees”), and immediate family members and/or those living in the same household of Employees are not eligible to participate in the Promotion.

  1. 3 Promotion Period: The Promotion begins on Wednesday 13th 2023 at 8:00am AEST and ends on January 31st 2024 at 12:00am, or when the supply of All Day Shred gifts is exhausted, whichever is earlier. Enhanced Australasias computer is the official time-keeping device for this Promotion.

  1. 4 How to Participate: To participate, place an order for the Summer Shred Stack during the promotion period. Every third order will be automatically entered to receive a complimentary tub of All Day Shred. No additional purchase or payment is necessary to participate or win.

  1. 5 Selection of Recipients: Recipients will be selected at random from every third order placed during the promotion period. Selection is subject to validation and verification of eligibility and compliance with all the terms and conditions set forth.

  1. 6 Notification: The selected recipients will be notified by email within 7 days following selection. Enhanced Australasia is not responsible for any recipient’s failure to receive notices due to spam, junk e-mail, or other security settings or for recipients’ provision of incorrect or otherwise non-functioning contact information.

  1. 7 Terms of Acceptance: A complimentary tub of All Day Shred will be sent to the address provided at the time of the order. The gift is non-transferable, and no substitution will be made except as provided herein at the Enhanced Australasia’s discretion.

  1. 8 Limitations of Liability: Enhanced Australasia is not responsible for any incorrect or inaccurate information, whether caused by website users, tampering, hacking, or by any equipment or programming associated with or utilised in the Promotion.

  1. 9 Right to Cancel or Modify: Enhanced Australasia reserves the right to cancel, terminate, modify or suspend the Promotion should virus, bug, non-authorised human intervention, fraud, or other cause beyond Enhanced Australasia’s control corrupt or affect the administration, security, fairness, or proper conduct of the Promotion.

  1. 10 Data Protection: By entering this promotion, you agree that Enhanced Australasia may use your personal information in accordance with its privacy policy for the purpose of administering this promotion.

  1. 11 Acknowledgment: By participating in this promotion, you have read and agreed to these terms and conditions.

  1. 12 Enhanced Australasia may request that you share your order and gift on social media by way of post (at your discretion).