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Updated: Jan 13, 2026
A Method to Study the Impact of Chemically-induced Ovarian Failure on Exercise Capacity and Cardiac Adaptation in Mice
Published on: April 7, 2014
The impact of tizanidine, thiocolchicoside, and cyclobenzaprine on vascular function in ovariectomized rats
Sümeyye Nur Gürsoy1, Tolga Esmerligil1, Uğur Berkay Inc1
1Department of Medical Pharmacology, Faculty of Medicine, Aydın Adnan Menderes University, Aydın, Turkiye.
Background/Aim:
Menopause is associated with increased vascular risk. This study investigated the effects of 3 centrally acting muscle relaxants-tizanidine (TZ), thiocolchicoside (TCC), and cyclobenzaprine (CBZ)-on vascular reactivity in ovariectomized (OVX) rats as a model of menopause.
Materials And Methods:
Body weight, blood glucose, blood pressure, and heart rate were recorded, and the rats underwent oophorectomy surgery. Eight weeks after the operation, the rats were divided into 5 groups: sham operated rats, OVX rats, OVX rats treated with TZ (OVX + TZ), OVX rats treated with TCC (OVX + TCC), and OVX rats treated with CBZ (OVX + CBZ). All drug treatments were at a dosage of 2 mg/kg/day for 2 weeks. Isolated rat aortas were suspended in a tissue chamber. Vascular reactivity was assessed using increasing concentrations of phenylephrine, acetylcholine, and sodium nitroprusside, as well as potassium chloride at a concentration of 40 mM.
Results:
Body weight, phenylephrine sensitivity, and potassium chloride responses significantly increased with OVX. TZ and CBZ decreased body weight gain and ameliorated receptor-dependent contractile sensitivity. TZ and CBZ had calcium antagonistic effects on vascular smooth muscle. TZ deteriorated endothelial function.
Conclusion:
TZ cannot be considered a safe medication for patients with endothelial dysfunction. In high doses and for longer periods, TCC and CBZ might also have deleterious effects on vascular reactivity. These findings are noteworthy from the perspective of rational drug therapy.
