# Bangpungtongsung-san alleviates depressive-like behavior and metabolic disturbances in high-fat diet-induced obesity: mechanisms involving inflammation, CREB/BDNF signaling, and NMDA receptor modulation

**Authors:** Bo-Ram Lee, No Soo Kim, Ui-Jin Bae, Yujin Choi, Changsop Yang, Mi Young Lee

PMC · DOI: 10.3389/fphar.2025.1565592 · Frontiers in Pharmacology · 2025-10-30

## TL;DR

Bangpungtongsung-san, a traditional herbal treatment, reduces depression-like behaviors and metabolic issues in obese mice by targeting inflammation and brain signaling pathways.

## Contribution

This study demonstrates that Bangpungtongsung-san improves both depression-like behaviors and metabolic disturbances in obese mice through multiple biological mechanisms.

## Key findings

- Bangpungtongsung-san reduced body weight and reversed metabolic abnormalities caused by a high-fat diet.
- The treatment decreased inflammation and restored BDNF signaling and NMDA receptor expression in the brain.
- Bangpungtongsung-san showed better combined behavioral and metabolic effects than fluoxetine or simvastatin.

## Abstract

Bangpungtongsung-san (BTS) is a traditional multi-herb preparation prescribed for obesity, but its role in obesity-associated depression remains unclear. We evaluated whether BTS alleviates depressive-like behaviors in high-fat diet (HFD) induced obese mice and elucidated the underlying mechanisms of its antidepressant potential.

Male C57BL/6N mice were randomized to normal diet (ND) or continuous HFD and maintained for 10 weeks. Throughout this period, mice were orally treated with BTS (30, 100, or 300 mg/kg), fluoxetine (FXT), simvastatin (SIM), or vehicle under identical chronic regimens. Body weight was monitored weekly. At week 10, metabolic parameters (blood glucose, plasma total cholesterol, triglycerides, HDL-C, and leptin) and depressive-like behaviors (tail suspension test and forced swimming test) were assessed. Subsequently, mechanistic analyses were performed to determine the effects of BTS on systemic and brain inflammatory responses, BDNF signaling, NMDAR expression, and serotonin (5-HT) signaling (Ido1, Tph2, and SERT) in the prefrontal cortex (PFC) and hippocampus (HPC).

A 10-week continuous HFD feeding produced robust weight gain, hyperglycemia, and elevated levels of total cholesterol (TCHO), triglycerides (TG), HDL-C, and leptin. Oral BTS treatment attenuated body weight gain and reversed these HFD-induced metabolic abnormalities (TCHO, TG, HDL-C, and leptin) in blood. Behaviorally, BTS-treated mice exhibited reduced immobility time compared to HFD group, indicating antidepressant-like effects. Mechanistically, BTS reduced systemic and brain pro-inflammatory cytokines (IL-1β and TNF-α) and normalized hippocampal GluN1/GluN2A/GluN2B protein levels together with BDNF expression restoration. BTS also elevated whole-brain 5-HT and tended to regulate SERT expression in HPC, supporting the enhanced synaptic 5-HT availability. Under identical chronic oral conditions, FXT showed partial antidepressant efficacy with minimal metabolic benefits, whereas SIM exhibited moderate metabolic improvements with limited behavioral effects. Comparatively, BTS provided superior therapeutic outcomes across both behavioral and metabolic parameters.

BTS ameliorated depression-like behaviors and metabolic dysfunction in HFD-induced obesity through coordinated modulation of inflammation, BDNF signaling, NMDAR expression, and 5-HT neurotransmission in the HPC. These findings support BTS as a promising multi-target candidate for treating comorbid depression and obesity.

## Linked entities

- **Genes:** BDNF (brain derived neurotrophic factor) [NCBI Gene 627], GRIN1 (glutamate ionotropic receptor NMDA type subunit 1) [NCBI Gene 2902], GRIN2A (glutamate ionotropic receptor NMDA type subunit 2A) [NCBI Gene 2903], GRIN2B (glutamate ionotropic receptor NMDA type subunit 2B) [NCBI Gene 2904], IDO1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 3620], TPH2 (tryptophan hydroxylase 2) [NCBI Gene 121278], SLC6A4 (solute carrier family 6 member 4) [NCBI Gene 6532]
- **Proteins:** BDNF (brain derived neurotrophic factor), GRIN1 (glutamate ionotropic receptor NMDA type subunit 1), GRIN2A (glutamate ionotropic receptor NMDA type subunit 2A), GRIN2B (glutamate ionotropic receptor NMDA type subunit 2B), SLC6A4 (solute carrier family 6 member 4)
- **Chemicals:** fluoxetine (PubChem CID 3386), simvastatin (PubChem CID 54454)
- **Diseases:** obesity (MONDO:0011122), depression (MONDO:0002050)

## Full-text entities

- **Genes:** Grin1 (glutamate receptor, ionotropic, NMDA1 (zeta 1)) [NCBI Gene 14810] {aka GluN1, GluRdelta1, GluRzeta1, M100174, NMD-R1, NMDAR1}, Lep (leptin) [NCBI Gene 16846] {aka ob, obese}, Grin2b (glutamate receptor, ionotropic, NMDA2B (epsilon 2)) [NCBI Gene 14812] {aka GluN2B, GluRepsilon2, NR2B, Nmdar2b}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Tph2 (tryptophan hydroxylase 2) [NCBI Gene 216343] {aka Ntph}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Slc6a4 (solute carrier family 6 (neurotransmitter transporter, serotonin), member 4) [NCBI Gene 15567] {aka 5-HTT, Htt, Sert}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], Creb1 (cAMP responsive element binding protein 1) [NCBI Gene 12912] {aka 2310001E10Rik, 3526402H21Rik, Creb, Creb-1}, Ido1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 15930] {aka Ido, Indo}, Grin2a (glutamate receptor, ionotropic, NMDA2A (epsilon 1)) [NCBI Gene 14811] {aka GluN2A, GluRepsilon1, NMDAR2A, NR2A}
- **Diseases:** obese (MESH:D009765), metabolic abnormalities (MESH:D008659), hyperglycemia (MESH:D006943), metabolic disturbances (MESH:D024821), inflammation (MESH:D007249), weight gain (MESH:D015430), depression (MESH:D003866)
- **Chemicals:** cholesterol (MESH:D002784), glucose (MESH:D005947), TG (MESH:D014280), 5-HT (MESH:D012701), FXT (MESH:D005473), Bangpungtongsung (-), SIM (MESH:D019821), fat (MESH:D005223)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** /6N — Mus musculus (Mouse), Transformed cell line (CVCL_D461)

## Full text

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## Figures

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## References

97 references — full list in the complete paper: https://tomesphere.com/paper/PMC12611972/full.md

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Source: https://tomesphere.com/paper/PMC12611972