Guggul (Commiphora mukul Hook.)

NOME COMUNE

Commiphora mukul (Guggul)

NOME SCIENTIFICO

Commiphora wightii (Hook. ex Stocks)

FAMIGLIA

Burseraceae

HABITAT

Commiphora mukul è una pianta spinosa che cresce in terreni poveri dell’India, Bangladesh e Pakistan, ma può essere trovato dal Nord Africa all’Asia centrale. Predilige i climi aridi e semi-aridi. Attraverso l’incisione della corteccia nella parte bassa della pianta si ricava una resina, chiamata gomma gugul. [1]

PARTE USATA

Gommoresina

PREPARAZIONI FARMACEUTICHE CONSIGLIATE

Estratto secco titolato in Guggulsteroni Z ed E min. 2,5%

COMPOSIZIONE CHIMICA

La frazione resinosa contiene lignani diarilfuranici come la sesamina e altri composti simili, diterpeni macrociclici detti cembrani, esteri dell’acido ferulico e carburi saturi poliidrossilati in C18, C 19 e C 20 detti guggultretoli e steroidi derivati dal colestano e dal pregnano. I composti principali sono i guggulsteroni E e Z, , che sono isomeri geometrici del pregnan-4,17(20)-diene-3,16-one. Essi sono accompagnati dai guggulsteroli. Nella frazione gommosa si ritrova un polisaccaride con molecola molto ramificata, costituito da D-galattosio, da L-arabinosio e dall’etere metilico in 4 dell’acido D-glicuronico.
Esiste anche una frazione volatile, costituita soprattutto da monoterpeni e in particolare da mircene, ma anche da alfa pinene, beta pinene, sabinene, alfa tuiene, limonene, 3-carene e beta elemene. [2]

PROPRIETA’ SALUTISTICHE

Azione su colesterolo e trigliceridi

Utilizzato per secoli nei principali sistemi di Medicina Tradizionale, in particolar modo nell’Ayurveda[5,32,33], secondo letteratura scientifica il guggulipide possiede capacità ipolipemizzanti e soprattutto ipocolesterolemizzanti, contribuendo a ridurre il colesterolo totale e il colesterolo LDL, aumentando la ratio colesterolo HDL/colesterolo totale [5,6,9,12,13,14,15,16,19,20].
Questa azione è dovuta in parte ad un aumento del numero dei recettori per le LDL posti sulla superficie degli epatociti e quindi ad un aumento del legame colesterolo/recettore [7], in parte ad uno stimolo sulla funzionalità della tiroide [11,49,50], i cui ormoni hanno notoriamente un effetto ipocolesterolemizzante e in parte anche ad un aumento dell’attività dell’enzima dopamina-beta-idrossilasi.
Dati recenti indicano che i guggulsteroni sono antagonisti del recettore X farnesoide, un recettore ormonale nucleare che è attivato dagli acidi biliari, e che provoca un aumento del colesterolo [9,35,36,37,51,52].

Dalla fine degli anni ’80 un crescente interesse scientifico per Guggul ha prodotto numerosi studi clinici per approfondirne i razionali di utilizzo nell’iperlipidemia, nell’ipercolesterolemia anche correlata a situazioni di obesità. Questi studi sono concordi nell’evidenziare che dopo assunzione per alcune settimane di estratto di guggul, si può osservare un’attività ipolipemizzante, con una riduzione media dei valori di colesterolo totale, colesterolo LDL e trigliceridi di circa il 13.5% [12,13,15,19]. Esami di laboratorio dimostrano anche che Guggul è in grado di prevenire l’ossidazione lipidica e di ridurre i fenomeni infiammatori, a carico delle cellule dei vasi sanguigni, che concorrono all’insorgenza delle malattie cardio-vascolari [5,7,22]. Secondo questi studi guggul dimostrerebbe la capacità di ridurre i livelli lipidici circolanti, determinando indirettamente un effetto cardioprotettivo [5].

AZIONE PREVALENTE

Ipolipidemizzante, ipocolesterolemizzante

Altre azioni

Antinfiammatoria, antiossidante

INDICAZIONI PRINCIPALI

Trattamento coadiuvante dell’ipercolesterolemia moderata anche correlata a stati di sovrappeso ed obesità

EFFETTI COLLATERALI

In alcuni pazienti può provocare nausea, eruttazioni e singhiozzo. A dosi elevate, come per l’assunzione di elevati dosaggi, in genere, di gommoresine, può causare diarrea, che regredisce prontamente con la sospensione del trattamento.

CONTROINDICAZIONI

Non è consigliabile in gravidanza e durante l’allattamento

INTERAZIONI CON FARMACI

Questa droga potrebbe ridurre l’assorbimento intestinale del propranololo e del diltiazem [28,58,59]

DATI TOSSICOLOGICI

Dati non disponibili

 

Bibliografia

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