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1.
China Journal of Chinese Materia Medica ; (24): 5957-5964, 2023.
Artículo en Chino | WPRIM | ID: wpr-1008793

RESUMEN

This study evaluated the clinical effectiveness of Ruyi Zhenbao Pills in the treatment of osteoarthritis, aiming to clarify its clinical advantages and promote rational drug use and related policy transformation. Following the relevant standards in Guidelines for the Comprehensive Evaluation of Drugs in Clinical Practice and Technical Specifications for the Clinical Comprehensive Evaluation of Chinese Patent Medicine, comprehensive research and related data on Ruyi Zhenbao Pills in the treatment of osteoarthritis were collected in the dimensions of safety, effectiveness, economy, innovation, suitability, accessibility, and traditional Chinese medicine(TCM) cha-racteristics(referred to as the "6+1" dimensions). Through evidence-based medicine, questionnaire surveys, health technology assessment, pharmacoeconomic evaluation, and other methods, a multi-criteria decision analysis(MCDA) model and CSC v2.0 software were used to comprehensively evaluate the clinical value of Ruyi Zhenbao Pills. Spontaneous reporting system data on adverse reactions and literature data indicate that the adverse reactions of Ruyi Zhenbao Pills are mostly general adverse reactions, with no reports of se-rious adverse reactions. The known risks are small, and its safety is rated as class A. It has been shown to effectively relieve joint pain and restore joint function in the treatment of osteoarthritis. However, more high-quality, large-sample randomized controlled trials are needed to further validate its effectiveness, which is rated as class B. There is evidence supporting its economic viability, and its economic is rated as class B. It demonstrates good clinical innovation, innovative enterprise service system, and industrial innovation, and innovation is rated as class A. Medical professionals and patients have a favorable perception of the suitability of Ruyi Zhenbao Pills, and further improvement can be made in terms of convenience of administration and promotion to facilitate rational drug use by healthcare professionals and patients. Suitability is rated as class B. The drug has a favorable price level, availability, and affordability, and accessibility is rated as class A. Ruyi Zhenbao Pills are a classic Tibetan medicinal prescription with excellent TCM theoretical characteristics. However, further research is needed on its use in human studies. TCM characteristics are rated as class B. Based on the evaluation results of the "6+1" dimensions, the comprehensive clinical evaluation is rated as grade B. Ruyi Zhenbao Pills have good clinical value in the treatment of osteoarthritis, and it is recommended to undergo the necessary procedures for conditional transformation into a policy for the management of essential clinical drugs.


Asunto(s)
Humanos , Medicina Tradicional China , Estándares de Referencia , Medicamentos sin Prescripción , Medicamentos Esenciales , Osteoartritis/tratamiento farmacológico , Medicamentos Herbarios Chinos/efectos adversos
2.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 82-89, 2022.
Artículo en Chino | WPRIM | ID: wpr-940764

RESUMEN

ObjectiveTo observe the intervention effect of Ruyi Zhenbao pills (RYZBP) on central pain after thalamic stroke in mice and explore the underlying mechanism. MethodThe central post-stroke pain syndrome (CPSP) model was induced by stereotactic injection of type Ⅳ collagenase into the hypothalamus in mice. The mice were divided into a sham group, a model group, low-, medium-, and high-dose RYZBP groups (0.65, 1.3, 2.6 g·kg-1), and a pregabalin group (0.075 g·kg-1). Seven days after modeling, the mice in the groups with drug intervention were administered with corresponding drugs by gavage according to the body mass, once per day for 25 days, while those in the sham group and the model group received an equal volume of normal saline. During this period, mechanical pain and cold pain were detected at different time points, and the apoptotic state of brain tissue cells was detected by in situ terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL). The 36 classical broad-spectrum inflammatory factors were quantitatively analyzed by liquid-phase chip technology, and differential molecules were screened out and verified by Western blot and enzyme-linked immunosorbent assay (ELISA). ResultCompared with sham operation group, mechanical pain threshold and cold sensitive pain threshold in model group were significantly changed (P<0.01). TUNEL results showed that apoptosis of brain cells was obvious. Western blot and ELISA results showed that the expressions of interleukin-1α (IL-1α) and chemokine ligand 5 (CCL5) increased in hypothalamus tissue and serum, while the expressions of Ang-2, granulocyte-colony-stimulating factor (G-CSF) and IL-4 decreased significantly (P<0.01). Compared with model group, RYZBW dose groups significantly increased mechanical pain threshold, decreased cold sensitivity pain threshold, decreased hypothalamus cell apoptosis ratio (P<0.01), decreased the expression of IL-1α and CCL5 in hypothalamus tissue and serum, while the expression of ANG-2, G-CSF and IL-4 were significantly increased (P<0.05). ConclusionRYZBP can relieve hyperalgesia in CPSP mice, and its mechanism is related to the regulation of the expression of pro-/anti-inflammatory factors IL-1α, CCL5, IL-4, G-CSF, and Ang-2.

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