Journal of Applied Pharmacy

Journal of Applied Pharmacy
Open Access

ISSN: 1920-4159

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Perspective - (2023)Volume 15, Issue 4

Regulation of Antimalarila Treatment Tolerance through Genetic Changes

Joseph Rajan*
 
*Correspondence: Joseph Rajan, Department of Bioinformatics, University of Alagappa, Tamil Nadu, India, Email:

Author info »

Description

Malaria, a potentially fatal mosquito-borne disease caused by the Plasmodium parasite, is a major worldwide health challenge, particularly in areas with inadequate access to healthcare resources. Effective antimalarial medication development has been a crucial component of malaria control efforts. These medications are critical in treating and preventing the spread of this disease. This article goes into the field of antimalarial medications, addressing their various varieties, mechanisms of action, problems, and possibilities for the future. Antimalarial medications are categorized according to their mode of action and chemical structure. Among the major types are: ACTs are now the most effective treatment for Plasmodium falciparum malaria, the most lethal type of the disease. Chloroquine and hydroxychloroquine are examples of medicines in this class. While chloroquine was formerly widely utilised, its efficiency has declined due to the advent of drug-resistant forms of the parasite. Hydroxychloroquine is still used in some circumstances and is being studied for potential repurposing against other disorders like COVID-19. Sulfadoxine-pyrimethamine and proguanil are drugs that target the parasite's capacity to synthesize folate, which is required for Deoxyribonucleic Acid (DNA) replication and cell division. However, resistance to these medications has evolved. Primaquine is an example of an aminoquinoline that is effective against Plasmodium vivax and Plasmodium ovale dormant liver-stage parasites (hypnozoites). It is critical for preventing the recurrence of certain malaria species. This medication, which is frequently used in conjunction with other antimalarials, has a lengthy halflife, making it effective for preventing recurrence. Chloroquine, for example, prevents parasites from breaking down hemoglobin, resulting in their death. Antifolate medications interfere with the synthesis of folate, a necessary precursor for nucleic acid synthesis, limiting the parasite's capacity to copy Deoxyribonucleic Acid (DNA) and Ribonucleic acid (RNA). Atovaquone, a medicine used in combination therapy, disrupts the parasite's electron transport pathway, causing it to lose energy. Artemisinin and its derivatives produce deadly reactive oxygen species within the parasite, causing cellular damage. The rise of drug-resistant parasites is one of the most important issues in malaria treatment. Resistance develops when parasites acquire genetic alterations that enable them to survive and grow in the face of medication exposure. Several antimalarial medications, notably chloroquine and sulfadoxine-pyrimethamine, have shown this effect. Combination therapy have become the standard of care for combating resistance. The use of two or more medications with separate modes of action reduces the probability of parasites developing resistance to both drugs at the same time.

ACTs are prime instances of combination therapy that have proven to be extremely successful in delaying the development of resistance. Malaria fight against malaria is developing, with continuing efforts to develop new antimalarial drugs and improve existing ones. Malaria treatment are investigating new pharmacological targets and repurposing existing medications.

To overcome resistance difficulties, novel molecules with distinct modes of action are being studied. Vaccines are being explored as a malaria prophylactic measure alongside medication development. RTS, the most sophisticated malaria vaccine, has clinical trials and is increasingly being implemented in numerous regions affected by malaria. Innovative malaria management options include genetic modification of mosquitos to render them incapable of transmitting the parasite and genetic manipulation of the parasite itself. Antimalarial medications are crucial in the fight against malaria, many lives have been saved, and the disease's impact on affected populations has been reduced.

Author Info

Joseph Rajan*
 
Department of Bioinformatics, University of Alagappa, Tamil Nadu, India
 

Citation: Rajan J (2023) Regulation of Antimalarila Treatment Tolerance through Genetic Changes. J Appl Pharm. 15:372.

Received: 01-Aug-2023, Manuscript No. JAP-23-26226; Editor assigned: 03-Aug-2023, Pre QC No. JAP-23-26226 (PQ); Reviewed: 17-Aug-2023, QC No. JAP-23-26226; Revised: 24-Aug-2023, Manuscript No. JAP-23-26226 (R); Published: 31-Aug-2023 , DOI: 10.35248/1920-4159.23.15.372

Copyright: © 2023 Rajan J. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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