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      Evaluation of Punarnavadi Mandura for haematinic activity against mercuric chloride-induced anemia in albino rats

      research-article
      , 1 ,
      Ayu
      Wolters Kluwer - Medknow
      Anemia, ferritin, mercuric chloride, Pandu, Punarnavadi Mandura

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          Abstract

          Background:

          Punarnavadi Mandura, a compound Ayurvedic formulation, is one of the most commonly used medicine in the treatment of anemia ( Pandu) in Ayurveda. The safety profile of this formulation is well established; however, no pharmacological study has been reported to provide the scientific basis for its use in the treatment of anemia.

          Aim:

          To evaluate the hematinic effect of Punarnavadi Mandura against mercuric chloride-induced anemia in albino rats.

          Materials and methods:

          The test drug ( Punarnavadi Mandura) was suspended in distilled water and administered orally in a dose of 450 mg/kg for 30 days in rats. Anemia was induced by simultaneous administration of mercuric chloride (9 mg/kg) for 30 consecutive days. Body weight was noted for each animals. At the end, haematological parameters, anaemia markers like serum iron, ferritin, and total iron binding capacity (TIBC), as well as relative weight of organs and histopathology investigation, were examined.

          Results:

          Exposure of mercuric chloride to rats for 30 days resulted in a significant decrease of body weight, an increase in the weight of the liver and kidney and a decrease in hemoglobin content. It also decreased serum ferritin to a significant extent and increased serum TIBC. Histopathology of the liver shows macro fatty changes, vacuolization, marked necrosis, and severe degenerative changes, while the kidney shows cell infiltration. All these changes were significantly attenuated by the administration of Punarnavadi Mandura.

          Conclusion:

          The present data indicate that Punarnavadi Mandura has possessing marked cytoprotective activity, significantly attenuated the HgCl 2-induced adverse changes on red blood cell related parameters, and showing hematinic activity in albino rats.

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          Most cited references61

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          Antioxidant Effects of Some Ginger Constituents

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            Oxidative mechanisms in the toxicity of metal ions.

            The role of reactive oxygen species, with the subsequent oxidative deterioration of biological macromolecules in the toxicities associated with transition metal ions, is reviewed. Recent studies have shown that metals, including iron, copper, chromium, and vanadium undergo redox cycling, while cadmium, mercury, and nickel, as well as lead, deplete glutathione and protein-bound sulfhydryl groups, resulting in the production of reactive oxygen species as superoxide ion, hydrogen peroxide, and hydroxyl radical. As a consequence, enhanced lipid peroxidation. DNA damage, and altered calcium and sulfhydryl homeostasis occur. Fenton-like reactions may be commonly associated with most membranous fractions including mitochondria, microsomes, and peroxisomes. Phagocytic cells may be another important source of reactive oxygen species in response to metal ions. Furthermore, various studies have suggested that the ability to generate reactive oxygen species by redox cycling quinones and related compounds may require metal ions. Recent studies have suggested that metal ions may enhance the production of tumor necrosis factor alpha (TNF alpha) and activate protein kinase C, as well as induce the production of stress proteins. Thus, some mechanisms associated with the toxicities of metal ions are very similar to the effects produced by many organic xenobiotics. Specific differences in the toxicities of metal ions may be related to differences in solubilities, absorbability, transport, chemical reactivity, and the complexes that are formed within the body. This review summarizes current studies that have been conducted with transition metal ions as well as lead, regarding the production of reactive oxygen species and oxidative tissue damage.
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              Molecular interactions with mercury in the kidney.

              R K Zalups (2000)
              Mercury is unique among the heavy metals in that it can exist in several physical and chemical forms, including elemental mercury, which is a liquid at room temperature. All forms of mercury have toxic effects in a number of organs, especially in the kidneys. Within the kidney, the pars recta of the proximal tubule is the most vulnerable segment of the nephron to the toxic effects of mercury. The biological and toxicological activity of mercurous and mercuric ions in the kidney can be defined largely by the molecular interactions that occur at critical nucleophilic sites in and around target cells. Because of the high bonding affinity between mercury and sulfur, there is particular interest in the interactions that occur between mercuric ions and the thiol group(s) of proteins, peptides and amino acids. Molecular interactions with sulfhydryl groups in molecules of albumin, metallothionein, glutathione, and cysteine have been implicated in mechanisms involved in the proximal tubular uptake, accumulation, transport, and toxicity of mercuric ions. In addition, the susceptibility of target cells in the kidneys to the injurious effects of mercury is modified by a number of intracellular and extracellular factors relating to several thiol-containing molecules. These very factors are the theoretical basis for most of the currently employed therapeutic strategies. This review provides an update on the current body of knowledge regarding the molecular interactions that occur between mercury and various thiol-containing molecules with respect to the mechanisms involved in the renal cellular uptake, accumulation, elimination, and toxicity of mercury.
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                Author and article information

                Journal
                Ayu
                Ayu
                AYU
                Ayu
                Wolters Kluwer - Medknow (India )
                0974-8520
                0976-9382
                Apr-Jun 2021
                16 March 2023
                : 42
                : 2
                : 103-109
                Affiliations
                [1]Department of Kaumarabhritya, IPGT and RA, Gujarat Ayurved University, Jamnagar, Gujarat, India
                [1 ]SDM Centre for Research in Ayurveda and Allied Sciences, Udupi, Karnataka, India
                Author notes
                Address for correspondence: Dr. V. K. Kori, Department of Kaumarabhritya, IPGT and RA, Gujarat Ayurved University, Jamnagar - 361 008, Gujarat, India. E-mail: drvkkori@ 123456yahoo.co.in
                Article
                AYU-42-103
                10.4103/ayu.AYU_294_20
                10158649
                db4bb3a2-dd31-4566-848f-9f0f20a9f433
                Copyright: © 2023 AYU (An International Quarterly Journal of Research in Ayurveda)

                This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

                History
                : 18 July 2020
                : 04 September 2020
                : 10 November 2022
                Categories
                Original Article

                Complementary & Alternative medicine
                anemia,ferritin,mercuric chloride,pandu,punarnavadi mandura
                Complementary & Alternative medicine
                anemia, ferritin, mercuric chloride, pandu, punarnavadi mandura

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