This study focused on the comprehensive characterization of the adsorbent obtained from rice husk, which was selected for its high adsorption capacity in iodine solution (IS) and methylene blue solution (MBS). This was achieved with adsorbents prepared by a combined treatment involving calcium carbonate prior to carbonization and activation with phosphoric acid. Characterization was performed using advanced techniques, such as scanning electron microscopy (SEM), atomic force microscopy (AFM), laser light diffraction and energy-dispersive X-ray spectroscopy (EDS), which allowed for the evaluation of the adsorbent’s microstructure and composition. The results revealed a complex structure of the adsorbents with interconnected pores, which facilitates efficient adsorption in IS and MBS and the standard indicators to evaluate adsorption capacity. The novelty of this study lies in the application of advanced characterization techniques to optimize the adsorbent properties and understand how preparation conditions affect the adsorbent’s microstructure. The characterized adsorbent materials in this study presented great potential for applications in water treatment and industrial processes, offering an economical and environmentally sustainable solution. Promoting the use of rice husks in the production of adsorbents contributes to the circular economy, reducing production costs and environmental pollution. The results suggested that these materials are effective in the removal of pollutants, which make them relevant for practical applications in water and soil bioremediation.

Vascular smooth muscle cells (VSMCs), the contractile cells in the tunica media of blood vessels, maintain vascular tone. The proliferation of VSMCs is an important feature of vascular remodeling that contributes to the regulation of blood pressure. Autophagy, an intracellular self-degrading process that delivers cytoplasmic constituents to lysosomes, plays a vital role in VSMC proliferation. This is regulated by the dopaminergic and renin–angiotensin systems but their interplay in their regulation of autophagy in VSMCs is not well-understood. In rat VSMCs, fenoldopam (Fen), a dopamine D1-like receptor agonist, increased autophagy, as determined by the increase in the protein expressions of microtubule-associated protein 1 light chain (LC)3-II and beclin-1 (BECN1), in a time- and concentration-dependent manner. Conversely, angiotensin II (Ang II), the endogenous Ang II type 1 receptor (AT₁R) agonist, decreased the protein expression of LC3-II and BECN1, also in a time- and concentration-dependent manner. The production of cyclic adenosine monophosphate (cAMP) and autophagic LC3-II puncta in VSMCs were increased by Fen and decreased by Ang II. Pre-treatment of VSMCs with Rp-cAMPS, a protein kinase A inhibitor, prevented the Fen-mediated increase and the Ang II-mediated decrease in LC3-II protein expression. Fen decreased, whereas Ang II increased the phosphorylation of P70S6K, a direct downstream mammalian target of rapamycin (mTOR). The inhibitory effect of Fen and stimulatory effect of Ang II on P70S6K phosphorylation were prevented by Rp-cAMPS. Ang II also decreased the Fen-mediated increase in cAMP production, while Fen attenuated the Ang II-mediated increase in cell proliferation, a response that occurs downstream of autophagy. Moreover, Ang II prevented the Fen-mediated inhibition of cell proliferation, an effect that was blocked by losartan, an AT₁R antagonist. These results demonstrate that Fen and Ang II counter-regulate autophagy and proliferation of VSMCs via the mTOR pathway, which is cAMP-dependent.