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Exploring the Fluconazole‐Resistance Modifying Activity and Potential Mechanism of Action of Fixed Oil from Caryocar coriaceum Wittm. (Caryocaraceae) against Candida Species

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AbstractThe fixed oil from the inner mesocarp of Caryocar coriaceum Wittm. is used in the Chapada do Araripe region of Brazil for the treatment of genitourinary candidiasis. This study aimed to evaluate the chemical composition, antifungal activity, reduction of fungal virulence, and the preliminary toxicity of the fixed oil from the inner mesocarp of C. coriaceum tested against three Candida yeasts. The oil was characterized by gas chromatography (GC‐MS and GC‐FID). Antifungal activity was assessed using the serial microdilution method. Additionally, the potential of the oil as an enhancer of fluconazole action was tested at sub‐inhibitory concentrations (MIC/8). The mechanism of action of C. coriaceum fixed oil was determined by evaluating the inhibition of morphological transition in Candida spp. The chemical composition of the fixed oil of C. coriaceum comprised both unsaturated and saturated fatty acids. Oleic (61 %) and palmitic (33 %) acids were the major constituents. Regarding its anti‐Candida activity, the oil inhibited the growth of C. albicans (IC50: 371 μg/mL) and C. tropicalis (IC50: 830 μg/mL). Furthermore, the oil reversed the antifungal resistance of C. albicans and C. tropicalis, restoring the susceptibility to fluconazole and reducing their IC50 from 12.33 μg/mL and 362 μg/mL to 0.22 μg/mL and 13.93 μg/mL, respectively. The fixed oil of C. coriaceum completely inhibited the morphological transition of C. albicans and C. tropicalis at a concentration of 512 μg/mL, but exhibited limited low antifungal potential against C. krusei. The observed antifungal activity may be attributed to the overproduction of reactive oxygen species. Additionally, the oil showed no toxic effect on the Drosophila melanogaster in vivo model. The fixed oil from the inner mesocarp of C. coriaceum emerge as a strong candidate for the development of new pharmaceutical formulations to treat infections caused by Candida spp.
Title: Exploring the Fluconazole‐Resistance Modifying Activity and Potential Mechanism of Action of Fixed Oil from Caryocar coriaceum Wittm. (Caryocaraceae) against Candida Species
Description:
AbstractThe fixed oil from the inner mesocarp of Caryocar coriaceum Wittm.
is used in the Chapada do Araripe region of Brazil for the treatment of genitourinary candidiasis.
This study aimed to evaluate the chemical composition, antifungal activity, reduction of fungal virulence, and the preliminary toxicity of the fixed oil from the inner mesocarp of C.
coriaceum tested against three Candida yeasts.
The oil was characterized by gas chromatography (GC‐MS and GC‐FID).
Antifungal activity was assessed using the serial microdilution method.
Additionally, the potential of the oil as an enhancer of fluconazole action was tested at sub‐inhibitory concentrations (MIC/8).
The mechanism of action of C.
coriaceum fixed oil was determined by evaluating the inhibition of morphological transition in Candida spp.
The chemical composition of the fixed oil of C.
coriaceum comprised both unsaturated and saturated fatty acids.
Oleic (61 %) and palmitic (33 %) acids were the major constituents.
Regarding its anti‐Candida activity, the oil inhibited the growth of C.
albicans (IC50: 371 μg/mL) and C.
tropicalis (IC50: 830 μg/mL).
Furthermore, the oil reversed the antifungal resistance of C.
albicans and C.
tropicalis, restoring the susceptibility to fluconazole and reducing their IC50 from 12.
33 μg/mL and 362 μg/mL to 0.
22 μg/mL and 13.
93 μg/mL, respectively.
The fixed oil of C.
coriaceum completely inhibited the morphological transition of C.
albicans and C.
tropicalis at a concentration of 512 μg/mL, but exhibited limited low antifungal potential against C.
krusei.
The observed antifungal activity may be attributed to the overproduction of reactive oxygen species.
Additionally, the oil showed no toxic effect on the Drosophila melanogaster in vivo model.
The fixed oil from the inner mesocarp of C.
coriaceum emerge as a strong candidate for the development of new pharmaceutical formulations to treat infections caused by Candida spp.

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