• =?UTF-8?Q?Chimpanzees_=e2=80=98self-medicate=e2=80=99_with_healing_?= =

    From Primum Sapienti@21:1/5 to All on Sun Jun 23 22:22:55 2024
    A followup of sorts on self medication in
    chimpanzees - something DD posted way
    back in 2022

    https://www.sciencedirect.com/science/article/pii/S0960982221017322
    Application of insects to wounds of self and
    others by chimpanzees in the wild


    The new research:

    https://www.science.org/content/article/chimps-use-more-plant-medicines-any-other-animal
    Chimps use more plant medicines than
    any other animal
    Study suggests sick chimpanzees go out of
    their way to find plants with antibacterial
    and anti-inflammatory properties

    For several decades, evidence has accumulated
    that animals turn to medicinal plants to
    relieve their ailments. Chimpanzees (and
    some other species) swallow leaves to
    mechanically clear the gut of parasites.
    Chimps also rely on the ingested pith of an
    African relative of the daisy, Vernonia
    amygdalina, to rid themselves of intestinal
    worms. Dolphins rub against antibacterial
    corals and sponges to treat skin infections.
    And recently, a male Sumatran orangutan was
    observed chewing the leaves of Fibraurea
    tinctoria, a South Asian plant with
    antibacterial and anti-inflammatory
    properties, and dabbing the juice onto a
    wound.
    ...


    https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0305219 Pharmacological and behavioral investigation
    of putative self-medicative plants in Budongo
    chimpanzee diets

    Abstract
    Wild chimpanzees consume a variety of plants
    to meet their dietary needs and maintain
    wellbeing. While some plants have obvious
    value, others are nutritionally poor and/or
    contain bioactive toxins which make ingestion
    costly. In some cases, these nutrient-poor
    resources are speculated to be medicinal,
    thought to help individuals combat illness.
    In this study, we observed two habituated
    chimpanzee communities living in the Budongo
    Forest, Uganda, and collected 17 botanical
    samples associated with putative
    self-medication behaviors (e.g., bark feeding,
    dead wood eating, and pith-stripping) or
    events (e.g., when consumer had elevated
    parasite load, abnormal urinalysis, or injury).
    In total, we selected plant parts from
    13 species (nine trees and four herbaceous
    plants). Three extracts of different
    polarities were produced from each sample using
    n-hexane, ethyl acetate, and methanol/water
    (9/1, v/v) and introduced to antibacterial and
    anti-inflammatory in vitro models. Extracts
    were evaluated for growth inhibition against
    a panel of multidrug-resistant clinical
    isolates of bacteria, including ESKAPE strains
    and cyclooxygenase-2 (COX-2) inhibition
    activity. Pharmacological results suggest that
    Budongo chimpanzees consume several species
    with potent medicinal properties. In the
    antibacterial library screen, 45 out of 53
    extracts (88%) exhibited ≥40% inhibition at a
    concentration of 256 μg/mL. Of these active
    extracts, 41 (91%) showed activity at
    ≤256μg/mL in subsequent dose-response
    antibacterial experiments. The strongest
    antibacterial activity was achieved by the
    n-hexane extract of Alstonia boonei dead wood
    against Staphylococcus aureus (IC50: 16 μg/mL;
    MIC: 32 μg/mL) and Enterococcus faecium (IC50:
    16 μg/mL; MIC: >256 μg/mL) and by the
    methanol-water extract of Khaya anthotheca
    bark and resin against E. faecium (IC50:
    16 μg/mL; MIC: 32 μg/mL) and pathogenic
    Escherichia coli (IC50: 16 μg/mL; MIC:
    256 μg/mL). We observed ingestion of both
    these species by highly parasitized
    individuals. K. anthotheca bark and resin
    were also targeted by individuals with
    indicators of infection and injuries. All
    plant species negatively affected growth
    of E. coli. In the anti-inflammatory COX-2
    inhibition library screen, 17 out of 51
    tested extracts (33%) showed ≥50% COX-2
    inhibition at a concentration of 5 μg/mL.
    Several extracts also exhibited
    anti-inflammatory effects in COX-2
    dose-response experiments. The K.
    anthotheca bark and resin methanol-water
    extract showed the most potent effects
    (IC50: 0.55 μg/mL), followed by the fern
    Christella parasitica methanol-water extract
    (IC50: 0.81 μg/mL). This fern species was
    consumed by an injured individual, a feeding
    behavior documented only once before in this
    population. These results, integrated with
    associated observations from eight months of
    behavioral data, provide further evidence
    for the presence of self-medicative resources
    in wild chimpanzee diets. This study addresses
    the challenge of distinguishing preventative
    medicinal food consumption from therapeutic
    self-medication by integrating pharmacological,
    observational, and health monitoring data—an
    essential interdisciplinary approach for
    advancing the field of zoopharmacognosy.

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