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Therapeutic Methods and Therapies TCIM
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1.
Mutagenesis ; 36(2): 177-185, 2021 05 31.
Article in English | MEDLINE | ID: mdl-33512444

ABSTRACT

The present study aimed to evaluate the effect of the manool diterpene on genomic integrity. For this purpose, we evaluated the influence of manool on genotoxicity induced by mutagens with different mechanisms of action, as well as on colon carcinogenesis. The results showed that manool (0.5 and 1.0 µg/ml) significantly reduced the frequency of micronuclei induced by doxorubicin (DXR) and hydrogen peroxide in V79 cells but did not influence genotoxicity induced by etoposide. Mice receiving manool (1.25 mg/kg) exhibited a significant reduction (79.5%) in DXR-induced chromosomal damage. The higher doses of manool (5.0 and 20 mg/kg) did not influence the genotoxicity induced by DXR. The anticarcinogenic effect of manool (0.3125, 1.25 and 5.0 mg/kg) was also observed against preneoplastic lesions chemically induced in rat colon. A gradual increase in manool doses did not cause a proportional reduction of preneoplastic lesions, thus demonstrating the absence of a dose-response relationship. The analysis of serum biochemical indicators revealed the absence of hepatotoxicity and nephrotoxicity of treatments. To explore the chemopreventive mechanisms of manool via anti-inflammatory pathways, we evaluated its effect on nitric oxide (NO) production and on the expression of the NF-kB gene. At the highest concentration tested (4 µg/ml), manool significantly increased NO production when compared to the negative control. On the other hand, in the prophylactic treatment model, manool (0.5 and 1.0 µg/ml) was able to significantly reduce NO levels produced by macrophages stimulated with lipopolysaccharide. Analysis of NF-kB in hepatic and renal tissues of mice treated with manool and DXR revealed that the mutagen was unable to stimulate expression of the gene. In conclusion, manool possesses antigenotoxic and anticarcinogenic effects and its anti-inflammatory potential might be related, at least in part, to its chemopreventive activity.


Subject(s)
Anticarcinogenic Agents/pharmacology , Colonic Neoplasms/drug therapy , DNA Damage/drug effects , Diterpenes/pharmacology , NF-kappa B/metabolism , Nitric Oxide/metabolism , Precancerous Conditions/drug therapy , Animals , Anticarcinogenic Agents/chemistry , Cell Line , Colonic Neoplasms/chemically induced , Cricetinae , Disease Models, Animal , Diterpenes/chemistry , Dose-Response Relationship, Drug , Doxorubicin/adverse effects , Etoposide/adverse effects , Hydrogen Peroxide/adverse effects , Male , Mice , Micronuclei, Chromosome-Defective/chemically induced , Micronucleus Tests , Mutagenicity Tests , Plant Extracts/pharmacology , Precancerous Conditions/chemically induced , Rats , Rats, Wistar , Salvia officinalis/chemistry
2.
J Ethnopharmacol ; 267: 113479, 2021 Mar 01.
Article in English | MEDLINE | ID: mdl-33091491

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Jarilla is the common name of an appreciated group of native plants from the semi-arid region in Argentina (Larrea cuneifolia Cav., Larrea divaricata Cav. and Zuccagnia punctata Cav.) that have been historically consumed to heal respiratory, musculoskeletal and skin ailments, as well as recommended for weakness/tiredness, hypertension, diabetes and cancer treatment. It was previously reported that some biological properties could be improved when these plants are used jointly. Infusions of a defined mixture, composed by three Jarilla species, L. cuneifolia: L. divaricata: Z. punctata (0.5:0.25:0.25) (HM2) showed synergistic and additive effect on antioxidant activity even after passing through the gastro-duodenal tract. AIM OF THE STUDY: The main purpose of this work was to evaluate antigenotoxic, antitumor, and anti-metastatic properties of the Jarilla species that grow in the Northwest of Argentina and a herbal combination of them. MATERIAL AND METHODS: Infusions of Jarilla mixture (HM2), and of each single plant species were prepared. Phenolic profiles of infusions were analyzed by HPLC-ESI-MS/MS and two relevant chemical markers were quantified. The antigenotoxic activity was evaluated by using the Ames test and the Cytokinesis-Block Micronucleus (CBMN) assay against direct mutagens. Evaluations of both cytotoxicity and antiproliferative effects were conducted on tumor and non-tumor cell lines. Both in vivo tumoral growth and metastasis inhibition were evaluated by using a carcinoma model on Balb/c mice. RESULTS: HM2 mix could suppress genetic and chromosome mutations induced by 4-nitro-o-phenylendiamine (4-NPD) and doxorubicin. Herbal mixture and single plant infusions showed cytotoxic effect against mammary, uterus, and brain tumoral cells without a selective action vs normal human cell line. HM2 mix was able to reduce mammary tumor mass on the Balb/c mice model and showed a significant reduction in the number of metastatic nodules in the lungs. CONCLUSIONS: Our results suggest that the combinations of three Jarilla species from northwest Argentina would be a promising alternative to treat or slow down the development of chronic diseases, such as cancer.


Subject(s)
Antimutagenic Agents/pharmacology , Antineoplastic Agents, Phytogenic/pharmacology , Cell Proliferation/drug effects , DNA Damage/drug effects , Fabaceae , Larrea , Neoplasms/drug therapy , Plant Extracts/pharmacology , Animals , Antimutagenic Agents/isolation & purification , Antineoplastic Agents, Phytogenic/isolation & purification , Argentina , CHO Cells , Cricetulus , Fabaceae/chemistry , HeLa Cells , Humans , Larrea/chemistry , MCF-7 Cells , Male , Medicine, Traditional , Mice, Inbred BALB C , Neoplasm Metastasis , Neoplasms/pathology , Phytotherapy , Plant Extracts/isolation & purification , Plants, Medicinal
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