Repository logo
 
Publication

Labdanum resin from Cistus ladanifer L. as a source of compounds with anti-diabetic, neuroprotective and anti-proliferative activity

dc.contributor.authorFrazão, David F.
dc.contributor.authorGomes, Carlos Martinsen_US
dc.contributor.authorSosa Diaz, Teresaen_US
dc.contributor.authorDelgado, F.M.G.
dc.contributor.authorGonçalves, José Carlos
dc.contributor.authorSilva, Amélia M.en_US
dc.date.accessioned2024-05-20T14:46:06Z
dc.date.available2024-05-20T14:46:06Z
dc.date.issued2024en_US
dc.date.updated2024-05-13T14:30:03Z
dc.description.abstractLabdanum resin or “gum” can be obtained from Cistus ladanifer L. by two different extraction methods: the Zamorean and the Andalusian processes. Although its main use is in the fragrance and perfumery sectors, ethnobotanical reports describe its use for medicinal purposes in managing hyperglycemia and mental illnesses. However, data concerning the bioactivities and pharmacological applications are scarce. In this work, it was found that the yield of labdanum resin extracted by the Andalusian process was 25-fold higher than the Zamorean one. Both resins were purified as absolutes, and the Andalusian absolute was purified into diterpenoid and flavonoid fractions. GC-EI-MS analysis confirmed the presence of phenylpropanoids, labdane-type diterpenoids, and methylated flavonoids, which are already described in the literature, but revealed other compounds, and showed that the different extracts presented distinct chemical profile. The potential antidiabetic activity, by inhibition of α-amylase and α-glucosidase, and the potential neuroprotective activity, by inhibition of acetylcholinesterase, were investigated. Diterpenoid fraction produced the higher α-amylase inhibitory effect (~30% and ~40% at 0.5 and 1 mg/mL, respectively). Zamorean absolute showed the highest α-glucosidase inhibitory effect (~14% and ~24%, at 0.5 and 1 mg/mL, respectively). Andalusian absolute showed the highest acetylcholinesterase inhibitory effect (~70% and ~75%, at 0.5 and 1 mg/mL, respectively). Using Caco-2 and HepG2 cell lines, Andalusian absolute and its purified fractions showed moderate cytotoxic/anti-proliferative activity at 24 h exposure (IC50 = 45–70 µg/mL, for Caco-2; IC50 = 60–80 µg/mL, for HepG2), whereas Zamorean absolute did not produce cytotoxicity (IC50 ≥ 200.00 µg/mL). Here we show, for the first time, that labdanum resin obtained by the Andalusian process, and its fractions, are composed of phytochemicals with anti-diabetic, neuroprotective and anti-proliferative potential, which are worth investigating for the pharmaceutical industry. However, toxic side-effects must also be addressed when using these products by ingestion, as done traditionally.
dc.description.versionN/A
dc.identifier.citationFRAZÃO, David F. [et al.] (2024) - Labdanum resin from Cistus ladanifer L. as a source of compounds with anti-diabetic, neuroprotective and anti-proliferative activity. Molecules. N.º 29, 2222. DOI: https://doi.org/10.3390/molecules29102222
dc.identifier.doi10.3390/molecules29102222en_US
dc.identifier.slugcv-prod-4080735
dc.identifier.urihttp://hdl.handle.net/10400.11/8980
dc.language.isoengpor
dc.relationUID/AMB/00681/2019en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectα-amylase
dc.subjectα-glucosidase
dc.subjectAcetylcholinesterase
dc.subjectCytotoxic activity
dc.subjectLabdanum resin
dc.subjectLabdane-type diterpenoids
dc.subjectMethylated flavonoids
dc.titleLabdanum resin from Cistus ladanifer L. as a source of compounds with anti-diabetic, neuroprotective and anti-proliferative activityen_US
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleMoleculesen_US
person.familyNameFranco Frazão
person.familyNameDelgado
person.familyNameGonçalves
person.givenNameDavid
person.givenNameFernanda
person.givenNameJosé
person.identifier508085
person.identifier.ciencia-id4913-7383-FB1A
person.identifier.ciencia-idC715-76B6-A07D
person.identifier.ciencia-idAE1F-12BE-65DD
person.identifier.orcid0000-0001-5017-6117
person.identifier.orcid0000-0003-1238-9386
person.identifier.orcid0000-0003-3387-4487
person.identifier.scopus-author-id7103325479
rcaap.cv.cienciaidC715-76B6-A07D | Fernanda Delgado
rcaap.rightsopenAccessen_US
rcaap.typearticleen_US
relation.isAuthorOfPublication4c55356e-318e-4c30-8b07-577d0c3d48cf
relation.isAuthorOfPublication8ae072f8-0aa1-46ce-830a-210c42f9e11b
relation.isAuthorOfPublication3f401604-ccbb-45f3-8ee1-05063cf3d60a
relation.isAuthorOfPublication.latestForDiscovery3f401604-ccbb-45f3-8ee1-05063cf3d60a

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
molecules-29-02222.pdf
Size:
692.77 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
2.02 KB
Format:
Item-specific license agreed upon to submission
Description: