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Khadijeh Haghighat , Fariba Mahmoudi , Homayoun Khazali,
Volume 12, Issue 3 (12-2024)
Abstract

Background: Chrysin is a natural bioactive compound belonging to the flavonoid group. The pain-relieving effects of chrysin have been reported in several studies; however, the molecular mechanism underlying its analgesic properties remains unknown. In the present study, the analgesic effect of chrysin was investigated on the hypothalamic Calcitonin Gene-Related Peptide (CGRP) and Tachykinin 1 (Tac1) gene expression in a formalin-induced pain model.
Methods: Twenty male rats weighing 200 ± 10 g were divided into four groups. Pain was induced by injecting 50 μl of formalin into the hind paw. The control and formalin groups received saline. In addition, 20 or 40 µg of chrysin was injected into pain-induced rats via the third cerebral ventricle. After 30 minutes, a behavioral test was conducted. Hypothalamus samples were then dissected, and real-time polymerase chain reaction (PCR) was performed to measure gene expression.
Results: The mRNA levels of CGRP and Tac1 significantly increased in the formalin-treated rats compared to the control group. In contrast, the mRNA levels of CGRP and Tac1 were significantly reduced in the chrysin-treated groups compared to the formalin group. Furthermore, the pain score was significantly lower in the chrysin-treated groups compared to the formalin group.
Conclusion: The pain-relieving effects of chrysin were mediated through the downregulation of hypothalamic CGRP and Tac1 in the pain model rats.

Malihe Bakhti, Farzaneh Taghian, Khosro Jalali Dehkordi , Rezvan Mirsafaei Rizi,
Volume 12, Issue 3 (12-2024)
Abstract

Background: Hypothyroidism is typically associated with a decreased basal metabolic rate, reduced energy expenditure, and weight gain. Exercise training and Dorema Aucheri (DA) have been identified as beneficial therapeutic strategies within complementary health approaches. Skeletal muscle metabolism and fiber type are regulated by innervation and soluble factors, such as thyroid hormones. However, the mechanisms between muscle function and hypothyroidism remain unclear.
Methods: Thirty mice were divided into five subgroups: the normal group; hypothyroid mice (HYPO, 8 mg/kg of propylthiouracil administered via intraperitoneal injection for 30 days); hypothyroid mice treated with DA (gavaged at 0.4 mg/kg for two months, five days per week); hypothyroid mice treated with exercise (75% VO2 max, 45 minutes per session, for two months, five days per week); and hypothyroid mice treated with both DA and exercise. The mRNA expression levels were detected via real-time qPCR.
Results: The data indicated that PPARγ, mTOR, and PI3K levels are reduced in hypothyroidism. DA and exercise enhanced PPARγ, mTOR, and PI3K levels in muscle tissue. Notably, DA and exercise significantly increased the expression levels of PPARγ, mTOR, and PI3K.
Conclusion: Exercise and DA, as alternative and complementary medicine, modified the PPARγ/mTOR/PI3K signaling pathways affected by hypothyroidism in mice.

 


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