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Objective: Enalapril has shown satisfactory potential in controlling increased and sustained blood pressure (BP). However, multiple dysregulated mechanisms that interact with each other and are involved in the pathophysiology of arterial hypertension may not be affected, contributing to the remaining cardiovascular risk. Using an exercise training protocol, we investigated whether adding both approaches to arterial hypertension management could promote higher modulation of regulatory mechanisms of BP in postmenopausal rats.

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Article Synopsis
  • Resiniferatoxin is a potent compound that can cause neuropathic pain and inflammatory responses, leading to the investigation of how blocking hepatoma-derived growth factor (HDGF) influences these effects.
  • The study used male Sprague-Dawley rats, divided into groups, to analyze the impact of HDGF blockage on mechanical pain thresholds and neuronal changes through various assays, including ELISA and immunofluorescence.
  • Results indicated that inhibiting HDGF improved pain responses, reduced inflammatory markers, and protected neuron cells in the spinal cord, suggesting that targeting HDGF might offer a new approach to pain relief beyond traditional painkillers.
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Delsoline, a major alkaloid of Hance, has both a curare-like effect and a ganglion-blocking effect and is used to relieve muscle tension or hyperkinesia. A ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was established for the determination of delsoline in mouse blood, and the pharmacokinetics of delsoline after intravenous administration (1 mg/kg) and intragastric administration (9, 6, and 3 mg/kg) were studied. Gelsenicine served as an internal standard, and a UPLC BEH C18 chromatographic column was used.

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Aims: Stromal interaction molecule 1 (STIM1) has emerged as an important player in the regulation of growth and proliferation of smooth muscle cells. Therefore, we hypothesized that STIM1 plays a crucial role in the maintenance of vascular integrity. The objective of this study was to evaluate whether reduced expression of STIM1 could modify the structure and function of the vasculature, leading to changes in blood pressure (BP).

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