Effects of catalpol on glycolipid homeostasis and lifespan of Drosophila melanogaster
Data files
Mar 11, 2026 version files 34.23 KB
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AKH.fasta
615 B
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BMM.fasta
2.42 KB
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Climbing_Assay.csv
703 B
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Fas2.fasta
5.05 KB
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Gly_S.fasta
2.61 KB
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HSL.fasta
2.80 KB
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Mean_Ages___Survival_Rate.csv
1.48 KB
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README.md
5.06 KB
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The_activities_of_trehalase.csv
645 B
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The_content_of_triglyceride__free_fatty_acid__insulin.csv
922 B
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The_contents_of_Carbohydrates.csv
931 B
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The_relative_expression_levels_of_genes.csv
2.52 KB
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TRE.fasta
2.89 KB
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Tret1-1.fasta
3.28 KB
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Tret1-2.fasta
1.80 KB
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Weight.csv
323 B
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Wing_Area.csv
186 B
Abstract
Glycolipid metabolism is a core regulatory link in the energy homeostasis and physiological functions of insects, directly affecting their survival, development, reproduction and environmental adaptability. Catalpol, the main active component of Rehmannia glutinosa, possesses multiple pharmacological activities such as antioxidation, anti-inflammation, and regulation of glycolipid metabolism. However, the specific regulatory mechanism of its effect on insect metabolism remains unclear. In this study, Drosophila melanogaster was used as the model organism to systematically explore the effects of catalpol on glycolipid metabolism, growth and development, motor ability, and lifespan of female adults, as well as its underlying molecular mechanism. Mechanistically, catalpol significantly promotes glucose catabolism, as demonstrated by increased activity of both soluble and membrane-bound trehalase and upregulation of the Tret1-1 gene. Concurrently, it dynamically regulated lipid metabolism, significantly increased the content of free fatty acids and triglycerides. This along with the upregulation of key lipolytic genes like hormone-sensitive lipase (HSL), indicated an accelerated fat turnover. These metabolic modulations translated into significant phenotypic improvements. Catalpol treatment promoted insect growth and development, evidenced by increased body weight, abdominal sizeand wing area. Furthermore, it enhanced their motor ability, shown by improved climbing, and extended their average lifespan and survival rate, suggesting a delay in aging. In conclusion, this study elucidates a novel regulatory model wherein catalpol dynamically modulates both glucose and lipid metabolism leading to improved growth, enhanced motor function, and extended lifespan in D. melanogaster. Our findings provide initial insights into the intricate mechanism-phenotype connection and provide compelling experimental evidence for catalpol potential as an insect physiological regulator. This research not only offers new perspectives on insect energy homeostasis but also lays a foundation for its application in agricultural pest control and beneficial insect breeding.
Dataset DOI: 10.5061/dryad.rr4xgxdnk
Description of the data and file structure
We conducted series of experimentsthis dataset is the experimental data derived from our manuscript, including weightdata, wing areadata, glycogencontent data, trehalose content data, glucosecontent data, solubletrehalaseactivitiedata, membrane-bound trehalaseactivitiedata, triglyceride contentdata, free fatty acid contentdata, insulin contentdata, qRT-PCR data, climb indexdata, survival rate dataand meanags data.
Files and variables
Fasta Files
File: BMM.fasta
File: Fas2.fasta
File: Gly_S.fasta
File: HSL.fasta
File: Tret1-1.fasta
File: TRE.fasta
File: Tret1-2.fasta File: AKH.fasta
Description: genetic sequences
Tabular Data
File: Climbing_Assay.csv
Description: Gently tap them until all the D. melanogaster reach the bottom of the tube, then stop tapping and start timing. After 10 seconds, observe and record the number of D. melanogaster that have reached 5 cm, 10 cm, and 20 cm or more respectively (%).
Variables
- 5d, 9d, 13d (the feeding duration for Drosophila melanogaster was 5 days, 9 days, and 13 days)
- Control, Catalpol (types of diet)
File: Mean_Ages___Survival_Rate.csv
Description: Calculate the number of surviving D. melanogaster in each tube at regular intervals every day (%), and finally calculate the average lifespan of D. melanogaster in each group (days).
Variables
- days
- Control, Catalpol (types of diet)
- 5d, 9d, 13d (the feeding duration for Drosophila melanogaster was 5 days, 9 days, and 13 days)
File: The_activities_of_trehalase.csv
Description: The homogenate was centrifuged at 1,000 g for 20 min at 4 C. Supernatant was used for protein determination, and soluble trehalase (TRE1) activity assays. The pellet was resuspended in 1PBS for membrane-bound trehalase (TRE2) activity analysis and protein determination (nmmol/ug pro).
Variables
- 5d, 9d, 13d (the feeding duration for Drosophila melanogaster was 5 days, 9 days, and 13 days)
- Control, Catalpol (types of diet)
File: The_content_of_triglyceride__free_fatty_acid__insulin.csv
Description: The triglyceride content was determined using the TAG content (mg/g) detection kit (Solarbio, China) based on the principle of the copper reagent method. Additionally, the free fatty acid (FFA) content (umol/L) was measured using the free fatty acid (FFA) content detection kit (Solarbio). Insulin levels (mU/L) were measured using a double-antibody one-step sandwich enzyme-linked immunosorbent assay (ELISA) kit (Shanghai Enzyme-linked Biotechnology Co., Ltd.).
Variables
- 5d, 9d, 13d (the feeding duration for Drosophila melanogaster was 5 days, 9 days, and 13 days)
- Control, Catalpol (types of diet)
File: The_contents_of_Carbohydrates.csv
Description: Protein concentration was measured using a BCA Protein Quantification Kit (Biyun Tian, China). Glucose and glycogen contents (nmol glucose/μg pro) were determined following the protocol provided with the Glucose Detection Kit (Sigma-Aldrich, USA), and trehalose content (nmol/μg pro) was measured via the anthrone method.
Variables
- 5d, 9d, 13d (the feeding duration for Drosophila melanogaster was 5 days, 9 days, and 13 days)
- Control, Catalpol (types of diet)
File: Weight.csv
Description: Each tube of D. melanogaster was weighed using an analytical balance, and then the number of D. melanogaster in each tube was counted and all the data were recorded. The average weight (mg) of each adult in each group was calculated.
Variables
- 5d, 9d, 13d (the feeding duration for Drosophila melanogaster was 5 days, 9 days, and 13 days)
- Control, Catalpol (types of diet)
File: The_relative_expression_levels_of_genes.csv
Description: qRT-PCR was performed using TB Green Premix Ex Taq II (Takara Bio) on a CFX96 Touch system (Bio-Rad, Germany). Reactions contained cDNA template, gene-specific primers, and master mix in a 20 L volume. Relative expression was calculated by the 2CT method.
Variables
- 5d, 9d, 13d (the feeding duration for Drosophila melanogaster was 5 days, 9 days, and 13 days)
- Control, Catalpol (types of diet)
File: Wing_Area.csv
Description: Microscopic images were captured and then processed using the Image J program for recognition and calculation. Set the program units according to the picture scale, precisely outline the exact cross - sectional area (mm2) contour of the D. melanogaster wings in the picture in the program.
Variables
- 5d, 9d, 13d (the feeding duration for Drosophila melanogaster was 5 days, 9 days, and 13 days)
- Control, Catalpol (types of diet)
Code/software
All data are saved in csv files and can be viewed through excel or other software capable of viewing csv files.
