TSH Suppression Induces Anxiety- and Depression-like Behaviors in Rats, With Hippocampal 5-HT Loss, Notch Activation, and a Neurogenesis-Apoptosis Imbalance

Indian Journal of Pharmaceutical Education and Research

  • Yikun Zhao1Clinical Medical College of China-Japan Friendship Hospital, Beijing University of Chinese Medicine, Beijing, CHINA.
  • Honglin Jiang2Department of Acupuncture and Mini-invasive Oncology, Beijing University of Chinese Medicine Third Affiliated Hospital, Beijing, CHINA.
  • Huiyuan Shang3Department of Chinese Medicine Surgery, China-Japan Friendship Hospital, Beijing, CHINA.
  • Zhongyuan Xia3Department of Chinese Medicine Surgery, China-Japan Friendship Hospital, Beijing, CHINA.

Volume 60 Issue 3 Pages 1256-1267

DOI: 10.5530/ijper.20264130

Abstract

Background: TSH suppression is widely used in thyroid cancer management; however, its neurobehavioral consequences are not well understood. Objectives: To evaluate the impact of TSH suppression on emotion-related behaviors, thyroid axis hormones, hippocampal serotonin (5-HT) levels, neurogenesis, Notch signaling, and apoptosis in a rat model. Materials and Methods: Rats were assigned to three groups: blank control, TSH replacement, and TSH suppression. TSH suppression was induced using total thyroidectomy combined with graded L-T4. Behavioral assessments were performed using open field and tail suspension tests. We measured serum levels of FT3, FT4, and TSH via ELISA, while hippocampal 5-HT levels were also quantified. Neural stem-cell proliferation and differentiation were assessed with BrdU, Nestin, NeuN, and GFAP immunohistochemistry. Notch signaling and apoptosis markers were analyzed using qPCR and Western blot techniques. Results: Compared with control and replacement groups, TSH suppression led to anxiety- and depression-like behaviors, demonstrated by greater immobility, longer rest periods, and delayed entry into the center of the open field. Additionally, we observed elevated FT3 and FT4 levels with reduced TSH, decreased levels of hippocampal 5-HT, and significant upregulation of Notch signaling pathway markers. Neurogenesis was disrupted, characterized by enhanced stem-cell proliferation but decreased neuronal differentiation, coupled with an increase in astrocyte differentiation. Furthermore, the Bax/Bcl-2 ratio increased, indicating a pro-apoptotic environment. Conclusion: The findings indicate that TSH suppression is linked to adverse mood-related behaviors, 5-HT depletion, Notch pathway activation, and an imbalance in neurogenesis and apoptosis. These results suggest that excessive suppression of the thyroid hormone axis may carry neuropsychiatric risks that need to be carefully balanced against the oncological benefits during thyroid cancer treatment.

Keywords

  • 5-HT
  • Bax/Bcl-2
  • Neurogenesis
  • Notch
  • Open field
  • Tail suspension
  • TSH suppression
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