The Effects of Cricket- and Beef-derived Protein on Plasma Amino Acid Concentrations and Appetite Responses

January 20, 2021 updated by: Tyler Churchward-Venne, McGill University

The Effects of Dietary Protein Source on Postprandial Plasma Amino Acid Availability, Gut-derived Appetite Regulating Hormones, and Subjective Appetite Sensations in Young Males

Dietary protein plays an important role in appetite regulation. Source of ingested dietary protein may have different effects on appetite, satiety, and/or food intake in humans. Insects are a rich source of protein consumed by many people around the world; however, the capacity of insect-derived protein to regulate appetite and food intake is unclear. The purpose of this study was to compare postprandial plasma glucose, insulin, amino acid, and appetite regulatory hormone concentrations, subjective appetite sensations, and food intake following the ingestion of 25 g of cricket- and beef-derived protein in healthy young males.

Study Overview

Detailed Description

With the rapid increase in the global population, the production of sufficient amounts of conventional animal-based protein to meet global dietary demands may no longer be desired nor feasible. Insects may represent an environmentally sustainable additional source of dietary protein that has the potential to help ensure global food security in the future. However, the functional characteristics of insect-derived proteins when fed to humans is unclear. Further, how insect-derived proteins compare to other animal-derived proteins (e.g. from beef) have not been explored.

The purpose of this study was to compare postprandial plasma glucose, insulin, and amino acid concentrations, gut-derived appetite regulatory hormones, subjective appetite sensations, and ad libitum energy intake following the ingestion of 25 g insect- or beef-derived protein in healthy young men. It was hypothesized that hyperaminoacidaemia would be more rapid following the ingestion of beef-derived protein compared to cricket-derived protein, although total amino acid availability would be similar between protein sources over a 300-minute postprandial period. It was further hypothesized there would be no difference between protein sources on postprandial subjective appetite sensations or subsequent ad libitum energy intake.

Study Type

Interventional

Enrollment (Actual)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Quebec
      • Montreal, Quebec, Canada, H2W 1S4
        • Exercise Metabolism and Nutrition Research Laboratory

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 35 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Male
  • Aged between 18-35 years inclusive
  • Healthy, moderately active
  • BMI < 30 kg/m2 and > 18.5 kg/m2
  • Having given informed consent

Exclusion Criteria:

  • Presence of any identified metabolic or intestinal disorders
  • Use of tobacco products
  • Adherence to a strict vegetarian or vegan diet
  • Use of medications known to affect protein metabolism
  • Allergy to shellfish or crustaceans
  • Allergy to beef protein
  • Engagement in physical exercise training more than 6 days per week

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: BASIC_SCIENCE
  • Allocation: RANDOMIZED
  • Interventional Model: CROSSOVER
  • Masking: QUADRUPLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Cricket-derived protein beverage
Ingestion of a cricket-derived protein beverage
Beverage containing 25 g cricket-derived protein
EXPERIMENTAL: Beef-derived protein beverage
Ingestion of a beef-derived protein beverage
Beverage containing 25 g beef-derived protein

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Plasma leucine concentration
Time Frame: 0-5 hours in the post-prandial period
umol/L
0-5 hours in the post-prandial period
Subjective appetite sensations (hunger, fullness, desire to eat, prospective food consumption)
Time Frame: 0-5 hours in the post-prandial period
mm (visual analogue scale)
0-5 hours in the post-prandial period

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Plasma branched-chain amino acid concentration
Time Frame: 0-5 hours in the post-prandial period
umol/L
0-5 hours in the post-prandial period
Plasma essential amino acid concentration
Time Frame: 0-5 hours in the post-prandial period
umol/L
0-5 hours in the post-prandial period
Plasma non-essential amino acid concentration
Time Frame: 0-5 hours in the post-prandial period
umol/L
0-5 hours in the post-prandial period
Plasma total amino acid concentration
Time Frame: 0-5 hours in the post-prandial period
umol/L
0-5 hours in the post-prandial period
Plasma glucose
Time Frame: 0-5 hours in the post-prandial period
mmol/L
0-5 hours in the post-prandial period
Plasma insulin
Time Frame: 0-5 hours in the post-prandial period
pmol/L
0-5 hours in the post-prandial period
Plasma GLP-1
Time Frame: 0-5 hours in the post-prandial period
pg/mL
0-5 hours in the post-prandial period
Plasma PYY
Time Frame: 0-5 hours in the post-prandial period
pg/mL
0-5 hours in the post-prandial period
Ad libitum food energy intake
Time Frame: assessed 5 hours after protein intake
kJ
assessed 5 hours after protein intake

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 28, 2019

Primary Completion (ACTUAL)

April 9, 2019

Study Completion (ACTUAL)

April 9, 2019

Study Registration Dates

First Submitted

January 15, 2021

First Submitted That Met QC Criteria

January 20, 2021

First Posted (ACTUAL)

January 22, 2021

Study Record Updates

Last Update Posted (ACTUAL)

January 22, 2021

Last Update Submitted That Met QC Criteria

January 20, 2021

Last Verified

January 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • A08-M28-18B

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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