# Wheat grain moxibustion ameliorates oxidative stress in PTU-induced hypothyroid rats via cAMP/PKA pathway activation

**Authors:** Jing Qin, Tingting Liu, Xiangyue Zhang, Xueni Chen, Jie Qin, Muhammad Shahzad Aslam, Huimin Feng, Yanhui Zhang, Xiaoxu Wang, Tiansheng Zhang, Chongyao Hao

PMC · DOI: 10.3389/fendo.2025.1612008 · Frontiers in Endocrinology · 2025-10-22

## TL;DR

Wheat grain moxibustion reduces oxidative stress in hypothyroid rats by activating the cAMP/PKA pathway, suggesting a potential therapy for hypothyroidism.

## Contribution

Demonstrates that wheat grain moxibustion alleviates hypothyroidism via cAMP/PKA pathway activation and oxidative stress reduction.

## Key findings

- Wheat grain moxibustion improved thyroid hormone levels and reduced oxidative stress markers in hypothyroid rats.
- Activation of the cAMP/PKA pathway was observed, with increased cAMP and PKA expression and CREB phosphorylation.
- Inhibition of the cAMP/PKA pathway reversed the beneficial effects of moxibustion on oxidative stress.

## Abstract

Hypothyroidism is a systemic hypometabolic disorder characterized by thyroid hormone deficiency and is closely associated with oxidative stress. The cAMP/PKA signaling pathway is critically involved in regulating thyroid hormone secretion and reducing oxidative stress. This study investigates whether wheat grain moxibustion alleviates hypothyroidism in a hypothyroidism model by attenuating oxidative stress and activating the cAMP/PKA signaling pathway.

The hypothyroid rat model was established by administering propylthiouracil. Following wheat grain moxibustion treatment, rat general condition, behavioral performance, and thyroid function were assessed. Then thyroid tissues and serum samples were collected. Thyroid tissue microstructure was examined by hematoxylin-eosin staining. Serum levels of triiodothyronine, thyroxine, thyroid-stimulating hormone, free triiodothyronine, free thyroxine, reactive oxygen species, malondialdehyde, catalase, superoxide dismutase, glutathione peroxidase, and cAMP were quantified using ELISA. Protein expression of signaling pathway components was detected via WB, while corresponding mRNA levels were measured by RT-PCR. To clarify the relationship between cAMP/PKA signaling and oxidative stress, the PKA inhibitor H-89 was administered to a subset of wheat grain moxibustion-treated rats.

Wheat grain moxibustion treatment ameliorated the general condition, behavioral performance, and thyroid hormone profiles in propylthiouracil-induced hypothyroid rats. Furthermore, it significantly reduced serum levels of reactive oxygen species and malondialdehyde, while enhancing the activities of catalase, superoxide dismutase, and glutathione peroxidase, collectively indicating attenuated oxidative stress. Concurrently, wheat grain moxibustion activated the cAMP/PKA pathway, demonstrated by elevated serum cAMP levels, downregulated phosphodiesterase 3A expression, upregulated PKA expression, and increased phosphorylation of CREB in thyroid tissues. Notably, pharmacological inhibition of this pathway with H-89 reversed the ameliorative effects of wheat grain moxibustion on oxidative stress.

Wheat grain moxibustion ameliorates oxidative stress in a propylthiouracil-induced hypothyroid rat model, mediated through activation of the cAMP/PKA signaling pathway. These results indicate its potential therapeutic utility in hypothyroidism management and mitigation of oxidative injury.

## Linked entities

- **Proteins:** PKA (cAMP dependent protein kinase), CREB1 (cAMP responsive element binding protein 1)
- **Chemicals:** propylthiouracil (PubChem CID 657298), H-89 (PubChem CID 449241), cAMP (PubChem CID 6076), malondialdehyde (PubChem CID 10964)
- **Diseases:** hypothyroidism (MONDO:0005420)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Creb1 (cAMP responsive element binding protein 1) [NCBI Gene 81646] {aka Creb}, Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, Pde3a (phosphodiesterase 3A) [NCBI Gene 50678] {aka RNPDE3A}
- **Diseases:** hypometabolic disorder (MESH:D009358), thyroid hormone deficiency (MESH:D018382), Hypothyroidism (MESH:D007037)
- **Chemicals:** PTU (-), malondialdehyde (MESH:D008315), triiodothyronine (MESH:D014284), eosin (MESH:D004801), reactive oxygen species (MESH:D017382), thyroxine (MESH:D013974), H-89 (MESH:C063509), hematoxylin (MESH:D006416), propylthiouracil (MESH:D011441)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

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## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12586185/full.md

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Source: https://tomesphere.com/paper/PMC12586185