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Tanycytic G6PT silencing prevents obesity induced by early postnatal overnutrition
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  • Published: 11 March 2026

Tanycytic G6PT silencing prevents obesity induced by early postnatal overnutrition

  • María José Barahona1,
  • Matías Vera2,3,
  • Carol Gajardo1,
  • Francisca López1,
  • Paul San Martín2 &
  • …
  • Francisco Nualart2,3 

Scientific Reports , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Cell biology
  • Endocrinology
  • Neuroscience
  • Physiology

Abstract

Tanycytes are ependymal glial cells that express the glucose-6-phosphate transporter (G6PT), which facilitates the incorporation of phosphorylated glucose from the cytosol into the reticular lumen. Herein, we show the antiobesogenic effects of G6PT-expressing tanycytes in a murine model of early postnatal overnutrition. Obesity in adult mice was induced by reducing litter size (SL mice) during the lactation period, a method that promotes excessive early nutrient intake. G6PT levels in tanycytes were analyzed using confocal-spectral microscopy. Tanycyte-specific G6pt silencing was carried out through the intracerebroventricular administration of AAV1-shG6pt-mCherry. Four weeks posttransduction, body weight, white adipose tissue weight, glucose metabolism and food intake were evaluated. We observed that SL mice exhibited reduced G6PT expression in tanycytes compared to mice with a normal phenotype. Remarkably, tanycyte-specific G6pt silencing in SL mice led to a significant reduction in body weight, accompanied by decreased adiposity. Furthermore, this intervention lowered blood glucose levels—restoring normoglycemia—and diminished food intake in response to fasting. These findings suggest that G6PT-expressing tanycytes may contribute to protective role against metabolic dysregulation. Targeting G6PT in tanycytes could help support the management and control of metabolic diseases.

Data availability

The data supporting the conclusions of this article are available upon reasonable request. To request the data, please contact María José Barahona.

References

  1. Rodriguez, E., Guerra, M., Peruzzo, B. & Blazquez, J. L. Tanycytes: A rich morphological history to underpin future molecular and physiological investigations. J. Neuroendocrinol. 31 (3), e12690 (2019).

    Google Scholar 

  2. Pasquettaz, R. et al. Peculiar protrusions along tanycyte processes face diverse neural and nonneural cell types in the hypothalamic parenchyma. J. Comp. Neurol. 529 (3), 553–575 (2021).

    Google Scholar 

  3. Barahona, M. J. et al. GLUT2 expression by glial fibrillary acidic protein-positive tanycytes is required for promoting feeding-response to fasting. Sci. Rep. 12 (1), 17717 (2022).

    Google Scholar 

  4. Barahona, M. J. et al. Glial hypothalamic inhibition of GLUT2 expression alters satiety, impacting eating behavior. Glia 66 (3), 592–605 (2018).

    Google Scholar 

  5. Lhomme, T. et al. Tanycytic networks mediate energy balance by feeding lactate to glucose-insensitive POMC neurons. J. Clin. Invest. 131(18), (2021).

  6. Barahona, M. J., Ferrada, L., Vera, M. & Nualart, F. Tanycytes release glucose using the glucose-6-phosphatase system during hypoglycemia to control hypothalamic energy balance. Mol. Metab. 84, 101940 (2024).

    Google Scholar 

  7. Arion, W. J., Wallin, B. K., Lange, A. J. & Ballas, L. M. On the involvement of a glucose 6-phosphate transport system in the function of microsomal glucose 6-phosphatase. Mol. Cell. Biochem. 6 (2), 75–83 (1975).

    Google Scholar 

  8. Kilkenny, C. et al. Improving bioscience research reporting: The ARRIVE guidelines for reporting animal research. J. Pharmacol. Pharmacother. 1 (2), 94–99 (2010).

    Google Scholar 

  9. Collden, G. et al. Neonatal overnutrition causes early alterations in the central response to peripheral ghrelin. Mol. Metab. 4 (1), 15–24 (2015).

    Google Scholar 

  10. Guillam, M. T. et al. Early diabetes and abnormal postnatal pancreatic islet development in mice lacking Glut-2. Nat. Genet. 17 (3), 327–330 (1997).

    Google Scholar 

  11. Barahona, M. J., Rojas, J., Uribe, E. A. & Garcia-Robles, M. A. Tympanic Membrane Rupture During Stereotaxic Surgery Disturbs the Normal Feeding Behavior in Rats. Front. Behav. Neurosci. 14, 591204 (2020).

    Google Scholar 

  12. Fuente-Martin, E. et al. Early postnatal overnutrition increases adipose tissue accrual in response to a sucrose-enriched diet. Am. J. Physiol. Endocrinol. Metab. 302 (12), E1586–E1598 (2012).

    Google Scholar 

  13. Bei, F. et al. Long-term effect of early postnatal overnutrition on insulin resistance and serum fatty acid profiles in male rats. Lipids Health Dis. 14, 96 (2015).

    Google Scholar 

  14. Hurtado-Alvarado, G. et al. Suprachiasmatic nucleus promotes hyperglycemia induced by sleep delay. Curr. Biol. 33 (20), 4343–4352e4 (2023).

    Google Scholar 

  15. Imbernon, M., Dehouck, B. & Prevot, V. Glycemic control: Tanycytes march to the beat of the suprachiasmatic drummer. Curr. Biol. 32 (4), R173–R176 (2022).

    Google Scholar 

  16. Rodriguez-Cortes, B. et al. Suprachiasmatic nucleus-mediated glucose entry into the arcuate nucleus determines the daily rhythm in blood glycemia. Curr. Biol. 32 (4), 796–805 (2022). e4.

    Google Scholar 

  17. Yu, Q. et al. Bitter taste cells in the ventricular walls of the murine brain regulate glucose homeostasis. Nat. Commun. 14 (1), 1588 (2023).

    Google Scholar 

  18. Dali, R., Estrada-Meza, J. & Langlet, F. Tanycyte, the neuron whisperer. Physiol. Behav. 263, 114108 (2023).

    Google Scholar 

  19. Du, H. et al. Specific reduction of G6PT may contribute to downregulation of hepatic 11beta-HSD1 in diabetic mice. J. Mol. Endocrinol. 50 (2), 167–178 (2013).

    Google Scholar 

  20. Sloop, K. W. et al. Specific reduction of hepatic glucose 6-phosphate transporter-1 ameliorates diabetes while avoiding complications of glycogen storage disease. J. Biol. Chem. 282 (26), 19113–19121 (2007).

    Google Scholar 

  21. Trinh, K. Y. et al. Perturbation of fuel homeostasis caused by overexpression of the glucose-6-phosphatase catalytic subunit in liver of normal rats. J. Biol. Chem. 273 (47), 31615–31620 (1998).

    Google Scholar 

  22. Rajas, F. et al. The glucose-6 phosphatase gene is expressed in human and rat small intestine: regulation of expression in fasted and diabetic rats. Gastroenterology 117 (1), 132–139 (1999).

    Google Scholar 

  23. Parker, J. C. et al. Plasma glucose levels are reduced in rats and mice treated with an inhibitor of glucose-6-phosphate translocase. Diabetes 47 (10), 1630–1636 (1998).

    Google Scholar 

  24. Muller, M. S., Fouyssac, M. & Taylor, C. W. Effective Glucose Uptake by Human Astrocytes Requires Its Sequestration in the Endoplasmic Reticulum by Glucose-6-Phosphatase-beta. Curr. Biol. 28 (21), 3481–3486 (2018). e4.

    Google Scholar 

  25. Steculorum, S. M. et al. Neonatal ghrelin programs development of hypothalamic feeding circuits. J. Clin. Invest. 125 (2), 846–858 (2015).

    Google Scholar 

  26. Kim, N., Kim, S., Park, S. & Kim, E. K. Adenosine transmission from hypothalamic tanycytes to AGRP/NPY neurons regulates energy homeostasis (Exp Mol Med, 2025).

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Funding

The work was supported by grants from the Agencia Nacional de Investigación y Desarrollo-ANID: “Fondecyt de posdoctorado” N°3210076 (to M.J.B), “Fondecyt de iniciación” N°11240089 (to M.J.B), and “Fondecyt regular” N° 1221147 (to F.N).

Author information

Authors and Affiliations

  1. Facultad de Ciencias, Universidad San Sebastián, Concepción, Chile

    María José Barahona, Carol Gajardo & Francisca López

  2. Centro de microscopía avanzada CMA BIO-BIO, Universidad de Concepción, Concepción, Chile

    Matías Vera, Paul San Martín & Francisco Nualart

  3. Laboratorio de Neurobiología y Células Madres (NeuroCellT), Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile

    Matías Vera & Francisco Nualart

Authors
  1. María José Barahona
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  2. Matías Vera
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  4. Francisca López
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  5. Paul San Martín
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Contributions

M.J.B, and F.N designed the experiments. M.J.B, C.G, M.V, F.L and P.S performed the experiments. M.J.B analysed the results. M.J.B wrote the manuscript. F.N reviewed the manuscript.

Corresponding authors

Correspondence to María José Barahona or Francisco Nualart.

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The authors declare no competing interests.

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Barahona, M.J., Vera, M., Gajardo, C. et al. Tanycytic G6PT silencing prevents obesity induced by early postnatal overnutrition. Sci Rep (2026). https://doi.org/10.1038/s41598-026-43136-0

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  • Received: 03 July 2025

  • Accepted: 02 March 2026

  • Published: 11 March 2026

  • DOI: https://doi.org/10.1038/s41598-026-43136-0

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Keywords

  • Tanycytes
  • Glucose-6-phosphate transporter
  • Energy balance
  • Obesity
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