# Investigating the Impact of Fasting and Refeeding on Blood Biochemical Indicators and Transcriptional Profiles in the Hypothalamus and Subcutaneous Adipose Tissue in Geese

**Authors:** Yi Liu, Xianze Wang, Guangquan Li, Shufang Chen, Huiyan Jia, Jiuli Dai, Daqian He

PMC · DOI: 10.3390/ani14182746 · 2024-09-23

## TL;DR

This study examines how fasting and refeeding affect blood chemistry and gene activity in geese, revealing metabolic and energy regulation changes.

## Contribution

The study identifies specific genes and metabolic pathways in geese hypothalamus and adipose tissue affected by fasting and refeeding.

## Key findings

- Fasting increases free fatty acids and glucagon while decreasing triglycerides, leptin, and insulin in geese blood.
- Fasting downregulates fatty acid synthesis genes (LPL, SCD, ACSL1) and upregulates PLIN2 in subcutaneous adipose tissue.
- Fasting alters hypothalamic gene expression, upregulating NOG, GABRD, and IGFBP-1 while downregulating POMC.

## Abstract

This study explores how geese respond to fasting and subsequent refeeding by analyzing changes in blood chemistry and gene activity in the hypothalamus and subcutaneous adipose tissues. After 24 h of fasting, geese’s blood levels of key substances such as fatty acids, glucagon, triglycerides, leptin, and insulin changed noticeably. The research also identified specific genes in the hypothalamus and subcutaneous adipose tissue that are influenced by fasting, providing insight into how geese regulate energy and maintain metabolic balance in response to changes in food intake.

Fasting and refeeding systems can cause significant short-term fluctuations in nutrient and energy levels, triggering adaptive physiological responses in animals. This study examines the effects of fasting and refeeding on blood biochemical indicators and transcriptional profiles in the hypothalamus and subcutaneous adipose tissue of geese. Biochemical assays reveal that fasting significantly increases levels of free fatty acids and glucagon, while reducing concentrations of triglycerides, leptin, and insulin. Transcriptomic analyses identify a complex transcriptional response in both the hypothalamus and subcutaneous adipose tissue, affecting several metabolic pathways and key genes associated with feed intake and energy metabolism. In subcutaneous adipose tissue, fasting downregulates genes involved in fatty acid synthesis (LPL, SCD, and ACSL1) and upregulates PLIN2, a gene promoting lipid droplet degradation. Fasting affects a variety of metabolic pathways and critical genes in the hypothalamus, including Apelin, insulin, and mTOR signaling pathways. After fasting, the mRNA expression of NOG, GABRD, and IGFBP-1 genes in the hypothalamus are significantly upregulated, while proopiomelanocortin (POMC) gene expression is markedly downregulated. This study highlights the intricate biological responses to nutritional changes in geese, which adds to our understanding of energy balance and metabolic regulation in avian species.

## Linked entities

- **Genes:** LPL (lipoprotein lipase) [NCBI Gene 4023], SCD (stearoyl-CoA desaturase) [NCBI Gene 6319], ACSL1 (acyl-CoA synthetase long chain family member 1) [NCBI Gene 2180], PLIN2 (perilipin 2) [NCBI Gene 123], NOG (noggin) [NCBI Gene 9241], GABRD (gamma-aminobutyric acid type A receptor subunit delta) [NCBI Gene 2563], IGFBP1 (insulin like growth factor binding protein 1) [NCBI Gene 3484], POMC (proopiomelanocortin) [NCBI Gene 5443]
- **Chemicals:** fatty acids (PubChem CID 264), glucagon (PubChem CID 16132283), leptin (PubChem CID 157010069), insulin (PubChem CID 70678557)

## Full-text entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, IGFBP1 (insulin like growth factor binding protein 1) [NCBI Gene 3484] {aka AFBP, IBP1, IGF-BP25, PP12, hIGFBP-1}, NOG (noggin) [NCBI Gene 9241] {aka SYM1, SYNS1, SYNS1A}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, GABRD (gamma-aminobutyric acid type A receptor subunit delta) [NCBI Gene 2563] {aka EIG10, EJM7, GABAARdelta, GEFSP5}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, SCD (stearoyl-CoA desaturase) [NCBI Gene 6319] {aka FADS5, MSTP008, SCD1, SCDOS, hSCD1}, APLN (apelin) [NCBI Gene 8862] {aka APEL, XNPEP2}, ACSL1 (acyl-CoA synthetase long chain family member 1) [NCBI Gene 2180] {aka ACS1, FACL1, FACL2, LACS, LACS1, LACS2}, LPL (lipoprotein lipase) [NCBI Gene 4023] {aka HDLCQ11, LIPD}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, PLIN2 (perilipin 2) [NCBI Gene 123] {aka ADFP, ADRP}
- **Chemicals:** triglycerides (MESH:D014280), free fatty acids (MESH:D005230), fatty acid (MESH:D005227), lipid (MESH:D008055)
- **Species:** Anser (geese, genus) [taxon 8842]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11428393/full.md

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Source: https://tomesphere.com/paper/PMC11428393