FRAMOMUM MELEGUETA - ALLIGATOR PEPPER.

FRAMOMUM MELEGUETA - ALLIGATOR PEPPER.

Synonym Aframomum grana-paradisi, Alpinia grana-paradisi, Amomum melegueta.Common name Alligator pepper, atar, graines de paradis, grains of paradise, grana paradise, grani de Meleguetta, grani de paradiso, guinea grains, malagettapfeffer, malaguette, nengrekondre pepre, paradies kõrner, paradijs korrels, poivre de Guinée.
Family Zingerberaceae (Ginger family).

Overview Alligator pepper is an herbaceous tropical perennial growing up to 5' tall; originally from West Africa, brought over to Surinam by the slaves.
It grows now abundantly in Suriname.

This plant has lanceolate leaves up to 9" long. The trumpet-shaped, purple flowers develop into 5 - 7 cm long grayish - brown, wrinkled dried pods (capsules) containing the numerous very small seeds. These are almost oval in shape, hard, shiny, and have a reddish-brown color.
The important parts of this plant are the seeds and rhizomes; the small (3-4 mm =1/8") reddish - brown seeds have a pungent aroma with a pepper - like heat.
This much sought after spice is tempered with, among others, flavors reminiscing of hazelnut, butter and citrus.
The essential oil from grains of paradise consists of two sesquiterpenes, humelene and caryophyllene and the oxides of these.
It has an exotic tropical scent and flavor and is used for the production of beer, wine and spirits, and the flavoring of vinegar.
It is used in the Surinam cuisine to flavor dishes such as vegetables (okra and tomatoes recipes), soups (lentil and chicken) and fish recipes.
The rhizome of the plant is used medicinally and is also is an important part from the diet of Western lowland gorillas in Africa.
Medicinal applications Used as a purgative, galactogogue (to increase production of breast milk), anthelmintic- and hemostatic agent (purifies the blood). It is also effective against schistosomiasis (bilharzia).
Further against intestinal infections, infestations; to calm indigestion and heartburn.
The seeds of Aframomum melegueta possess potent anti-inflammatory activity with a favorable gastric tolerability profile.

Aframomum may successfully be used to treat diseases where inflammation is in play like cardiovascular conditions, arthritis, osteoporosis and Alzheimer's disease.
There are some reports of the use of this pant as an aphrodisiac and testosterone booster.
It may also have anti estrogenic properties.
Aframomum may have a superior ability to counteract skin irritation.
It is used in West Africa for alleviating stomachache and diarrhea as well hypertension.
Phytochemical analysis revealed the presence of alkaloids, cardio glycosides, tannins, flavonoids, sterols, triterpenes, and oils, while the methanol fraction contains alkaloids, glycosides, tannins, flavonoids, sterols, and resins.
The pungent, peppery taste of the seeds is caused by aromatic ketones such as (6)-paradol; the essential oils occur only in traces.

Hardiness USDA zone 9 - 11.
Propagation Seeds and rhizomes.
Culture Full sun / partial shade; well drained soil.
It needs high humidity.
Plant in frost free spots.

http://www.tropilab.com/nengrekondrepepre.html

Aframomum melegueta (Grains of paradise) is not Alligator pepper part 2

Posted on February 10, 2014 by Ayo

 “I put a few between my teeth and crunched. They cracked like coriander releasing a billowing aroma, and then a slowly intensifying heat, like pepper at the back of my mouth. The taste changes in a second. The heat lingered. But the spice flavor was pleasantly tempered, ripe with flavors reminiscent of jasmine, hazelnut, butter and citrus, and with the kind of oiliness you get from nuts. They were entirely different from black peppercorns and in my mind, incomparably better.”                                                                                                         

Amanda Hesser, New York times, 2000

Can you make a Guess what all those  Paean is for?

It is for……………………..Aframomum  melegueta (Grains of paradise).
Let’s know a little about Aframomum  melegueta (A. melegueta)

A.melegueta is a known name when listing the medicinal, aromatic tropical plants that exist. This is not only because of its various uses but also the historical value attached to it.

The first known reference to the plant dates from 1214 A.D., there were remarks that physicians in places as far apart as the Frankish Court at Nicosia, Rome, Lyons and Wales included this plant in medical prescriptions. Queen Elizabeth I of England was  also noted to flavour her Beer with it (Harten, 1970).
Around the 14th-15th Century, Pliny mentioned it to be African pepper and it was later referred to as Grains of Paradise when it became a popular substitute for Black pepper in Europe.

king Afonso_V of Portugal
(public domain image)

In 1469, it was given another name; Malagueta (a Portuguese word which literally means ‘chilli pepper’) and gained more popularity as it was included in the trade by a Portuguese merchant and explorer from Lisbon; Fernao Gomes, in the Gulf of Guinea following the permission of King Afonso V of Portugal.  Around these centuries, Menagier de Paris(French medieval book on a woman’s proper behaviour in marriage and running a household since 1393) recommended it for improving wine that smells stale, also, the present region now known as Liberia was named ‘Grains coast’ (adapted fromGrains of paradise) because its seeds were  major export item in the region at that period.

The first scientific puplication on this plant was done by Karl Moritz Schumann on the 4th October, 1904. A.melegueta  is also commonly called Guinea grains and erroneously Alligator pepper!

Wait a minute……Is this Alligator pepper or A. melegueta???

Characteristics  of A.melegueta
A.melegueta is a perennial deciduous herb native to the tropics and grows at the swampy habitats of the West Africa coast. It belongs to the Ginger family (Zingiberaceae). It possesses tufted leafy stem that can be up to 1.5m high. The leaves are simple, alternate and lanceolate. The matured leaves can grow as long as 40cm in length  and 12cm-15cm wide. It produces purple coloured flowers which develops into pods that can be as long as 8cm and about 3cm wide. This pod contains  numerous reddish-brown seeds (can be as many as 300 seeds in one pod).    The sharp and peppery taste of the seeds is caused by the aromatic ketones;   6-paradol, 6-gingerol and 6-shogaol present in it (Sugita et al, 2013). The fruits are fleshy, indehiscent and produce spikes. It cannot survive temperatures below 1°C.

 

A.melegueta dissected pod and its seeds

Taxonomic classification
Kingdom: Plantae
Division: Magnoliophyta
Class: Liliopsida
Order: Zingiberales
Family: Zingiberaceae
Genus: Aframomum
Species: Aframomum melegueta

Synonyms of A. melegueta

• Aframomum grana-paradisi (L.) K.Schum.
• Aframomum meleguetella K.Schum.
• Alexis grandiflora (Sm.) Salisb.
• Alpinia grana-paradisi (L.) Moon
• Amomum elatum Salisb. [Illegitimate]
• Amomum grana-paradisi L.
• Amomum grandiflorum Sm.
• Amomum melegueta Roscoe [Illegitimate]
• Amomum melegueta var. violacea Ridl.
• Cardamomum grana-paradisi (L.) Kuntze
• Cardamomum grandiflorum (Sm.) Kuntze
• Torymenes officinalis Salisb. [Illegitimate]

Common names of A.melegueta

Distribution of A. melegueta
It is native to  the West African region. The distribution map below shows that it can be found in Nigeria, Uganda, Angola,Benin, The Gambia, Ghana, Guinea, Cote d’Ivoire(Ivory Coast), Liberia,, Sierra Leone, Togo, Cameroon,Congo, Gabon, Gulf of Guinea Is., Democratic Republic of the Congo (Zaire), Guinea-Bissau  but widely cultivated in  various parts of  other tropical Africa, South America and several other places.

A. melegueta and its Medicinal uses

Medicinal uses of A.melegueta ranges from;

•  anti-inflammatory capabilty;
•  antimicrobial activities ;
• Preventing/healing  dental problem, Asthma and Body weakness ;
• increasing whole-body energy expenditure by its  oral ingestion
• protective capacity  on crops such as Zea mays (Maize) and more medicinal uses are being discovered on daily basis

A.melegueta and Culinary uses
The heat is what has kept it alive in people’s minds.  It can be mixed with coriander, cinnamon, dried chilies and cloves as a condiment for grilled lamb, chicken, fish, pumpkin and okra, or added to soups, stews and pickling mixtures. They can also be found in ‘raz al hanout’, the spice mixture of Morocco (Hesser, 2000).

”Yummy’‘, nothing tastes better than its  flavour around your meals……you might want to give it a try today!!!

A.melegueta and Culture

When a baby is born in Africa, for instance, in the Yoruba culture(Nigeria), a small amount  is given to them to taste, this is done minutes after they are born. It is said to be a welcoming process for the baby. It is also used as a traditional wedding gift in the same Yoruba culture. In addition to this, A.melegueta together with kola nut is served to guests in the Eastern part of Nigeria. When chewed together, the hot spicy taste enhances or reduces the bitter taste from the kola nut.               A.melegueta is used for divination and ordeal to determine who is guilty of an offence among the Efik people (primarily Eastern part of Nigeria). It is also used for religious (voodoo) rites at the Caribbean Islands.
One of the myths as regards this seed is that it prevents accident when swallowed and also reduce the state of drunkenness ( you might give this myth a try when you feel tipsyBUT NOT  with Accident!).

Here, is the BIG BOOM……………….
A.melegueta is NOT ALLIGATOR PEPPER

The  seed of Alligator pepper is from A. danielli, A. citratum or A. exscapum. The spice grows wild in countries like Nigeria, Ghana, Guinea and Liberia.  The English name –Alligator pepper becomes very obvious when the pod is open and the seeds are shown, the seeds have a papery skin enclosing them and the bumps of the seeds within this skin looks like that of an alligator’s back.   The  alligator pepper is sold as an entire pod which contains the seed unlike the grains of paradise which is sold as only seeds. It is highly aromatic than that of  A.melegueta (Grains of paradise) seeds.

It is worthy to note that this same plant generally known as Alligator pepper by a Lay-man in many countries (i.e Nigeria) is also been refered to as  A.melegueta ( Grains of Paradise) by the botanical researchers in that region.

The Ultimate search for what is correct!

After thorough investigation using different search engines available, it was discovered that larger number of  Researchers(all around the globe) that  have worked on  A. meleguetaused Alligator pepper as one of its common names while very few others tried to differentiate them. 

The question is: How do we know for sure which seeds of genus Aframomum  was used by these Researchers;  A. melegueta or Alligator pepper(from A. danielli, A. citratumor A. exscapum)?                                                                                                            This crucial question points to the fact that there is need for  comprehensive research that will succintly clarify the differences among these species of Aframomum  as it appears that most of the focus as been on the uses of these plants.

……..while the hunt for the right seed-identity of  what Queen Elizabeth I of England used to flavour her Beer continues……please know that the English common names ofA.melegueta are  Grains of paradise, Guinea grains BUT not Alligator pepper!!!

You might also want to read my previous post on these species.

References

All images, video and Map were created by the Blogger.

Betumiblog (2013). Grains of Paradise or Alligator Pepper? 
URL: http://betumiblog.blogspot.co.uk/2013/01/grains-of-paradise-or-alligator-pepper.html.  [15 October 2013]

Echo I.A., Osuagwu A.N., Agbor R.B., Okpako E.C, and Ekanem B.E. (2012)
Phytochemical Composition of Aframomum melegueta and Piper guineense Seeds. World Journal of Applied Environmental Chemistry.  2(1): 17-21

Harten A.M. (1970). Melegueta pepper. Economic Botany.  24(2): 208-216.

Hesser A. (2013). What Peppercorns Only Dream of Being. URL:  http://www.nytimes.com/2000/05/03/dining/what-peppercorns-only-dream-of-being.html?pagewanted=all&src=pm [23 October 2013]

IPNI (2005). Plant name details. URL: http://www.ipni.org/ipni/idPlantNameSearch.do?id=871877-1.   [1 November 2013]

Liberian Forum.com (2006). America colonization society. URL: http://liberianforum.com/liberianfacts.htm. [1st January, 2014].

Multilingual Multiscript plant Name database(2001). Sorting Aframomum names. http://www.plantnames.unimelb.edu.au/Sorting/Aframomum.html#melegueta. [ 2nd  January, 2013].

Odugbemi T. (2008).  A textbook of Medicinal plants in Nigeria. Lagos: Tolu Odugbemi.

Sugita J, Yoneshiro T, Hatano T, Aita S, Ikemoto T, Uchiwa H, Iwanaga T, Kameya T, Kawai Y and Saito M.( 2013). Grains of paradise (Aframomum melegueta) extract activates brown adipose tissue and increases whole-body energy expenditure in men. British Journal of Nutrition. 110(4): 733-738

The Plant List(2010). Aframomum melegueta K.Schum.  Version 1. URL: http://www.theplantlist.org/tpl/record/kew-218399. [1st November, 2013].
Ukeh D.A., Umoetok S.B.; Bowman A.S., Mordue A.J., Pickett J.A., and Birkett M.A. (2011). Alligator pepper; Aframomum melegueta, and Ginger;Zingiber officinale, reduce stored maize infestation by the maize weevil, Sitophilus zeamais in traditional African granaries.  Crop protection. 32 : 99-103.

The Sleuth Journal(2013). An herb for Thought: Alligator pepper . URL: http://www.thesleuthjournal.com/herb-thought-alligator-pepper/. [12th December, 2013].

Wikipedia (2013). Alligator pepper. URL: http://en.wikipedia.org/wiki/Alligator_pepper.  [21 October 2013].

https://blogs.reading.ac.uk/tropical-biodiversity/2014/02/aframomum-melegueta-grains-of-paradise-is-not-alligator-pepper/

Toxicological evaluation of Grains of Paradise (Aframomum melegueta) [Roscoe] K. Schum

Nebojsa Ilic,b Barbara M. Schmidt,a Alexander Poulev,a and Ilya Raskina,*

Author information ► Copyright and License information ►

The publisher's final edited version of this article is available at J Ethnopharmacol

See other articles in PMC that cite the published article.

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Abstract

Ethnopharmacological relevance

Grains of Paradise (Aframomum melegueta [Roscoe] K. Schum.) seeds are used in West Africa as a remedy for variety of ailments such as stomachache, snakebite, diarrhea and they have reported anti-inflammatory properties. Additionally, the seeds contain gingerols and related compounds that may be useful against cardiovascular disease, diabetes, and inflammation.

Aim of study

A 28-day sub-chronic toxicity study in male and female Sprague Dawley rats was conducted to evaluate the safety of a Grains of Paradise extract.

Materials and methods

An ethanolic extract of the seeds was evaluated for toxicological effect on rats.

Results

A dose-related increase in absolute and relative liver weights was observed in males and females dosed with 450 and 1500 mg/kg. There was a corresponding increase in alkaline phosphatase with no signs of steatosis or cirrhosis. At the same doses, there was a significant decrease in blood glucose in male rats.

Conclusions

This study shows that Grains of Paradise extract may be useful as a treatment for diabetes, however liver toxicity should be considered.

Keywords: Aframomum melegueta, gingerols, liver toxicity, alkaline phosphatase, dietary supplement

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1. Introduction

Grains of Paradise (Aframomum melegueta [Roscoe] K. Schum.), also known as Guinea pepper or Alligator pepper, is a member of the Zingiberaceae family native to West Africa. It is a herbaceous perennial plant that grows up to 1.5 meters height, with purple flowers that develop into 5 to 7 cm long pods containing small, reddish-brown aromatic and pungent seeds. In the region of West Africa the seeds are used as a spice for flavoring food and have a wide range of ethnobotanical uses. They are used as a remedy for treating stomachache, diarrhea, and snakebite (Akendengue and Louis, 1994; Umukoro and Ashorobi, 2007). Also it has been shown that aqueous seed extract had anti-inflammatory and peripheral analgesic activity (Umukoro and Ashorobi, 2001). Grains of Paradise are very rich in the non-volatile pungent compounds gingerols, shogaols, paradols, and related compounds (Connell, 1970; Connell and McLachlan, 1972; Tackie et al., 1975). Similar compounds are found in many species of the Zingiberaceae family including ginger (Zingiber officinale Roscoe), turmeric (Curcuma longa Linnaeus), and cardamom (Amomum cardamomum Linnaeus). Gingerols have reported blood glucose lowering (Al-Amin et al., 2006) and anti-inflammatory (Tjendraputra et al., 2001; Jolad et al., 2005) activities, which may be useful for treating diabetes and cardiovascular disease. Therefore, toxicology studies were initiated to evaluate the safety of using Grains of Paradise extract as a botanical therapeutic.

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2. Materials and methods

2.1 Plant material and extraction

Seeds of Aframomum melegueta [Roscoe] K. Schum. were purchased from a commercial supplier from Abidjan, Ivory Coast and identified by Dr. L. Struwe, Rutgers University. A voucher specimen (Struwe 1424 CHRB) was deposited at the Chrysler Herbarium, Rutgers University, New Brunswick, USA.

A single batch of dry Grains of Paradise seeds were extracted in 95% ethanol (1:10 w/v) for 24 h at room temperature (24 °C) with continuous agitation provided by a platform shaker. The resulting ethanolic extract was filtered and the solvent was removed under vacuum, using a rotary evaporator (yield of the extract: 2%). The extract was stored at 4 °C.

2.2 LC-MS analysis

To determine the chemical constituents, Grains of Paradise extract was separated and analyzed with a Waters (Milford, MA) LC-MS Integrity system consisting of a solvent delivery system including a W616 pump and W600S controller, W717 plus auto-sampler, W996 PDA detector and Waters TMD Thermabeam electron impact (EI) single quadrupole mass detector. Data were collected and analyzed with the Waters Millennium v. 3.2 software, linked with the 6th edition of the Wiley Registry of Mass Spectral Data, containing 229,119 EI spectra of 200,500 compounds. Substances were separated on a Phenomenex Luna C-8 reverse phase column, size 150 × 2 mm, particle size 3 µm, pore size 100 Å, equipped with a Phenomenex Security Guard pre-column. The mobile phase consisted of 2 components: solvent A (0.5% acetic acid in double distilled de-ionized water, pH 3–3.5), and solvent B (100% acetonitrile). The mobile phase flow was adjusted at 0.25 ml/min, and generally a gradient mode was used for all analyses. The gradient points were for time 0.0 min – 95% A and 5% B; for time 35.0 min – 5% A and 95% B; held isocratic for 5 minutes and from 40.0 min to 45.0 min. – back to initial conditions of 95% A and 5% B. A column equilibration time of 15 min was set between subsequent injections.

2.3 Animals

The Sprague-Dawley derived rat was the system of choice because, historically, it has been the preferred and commonly used species for oral toxicity tests. Fifty Hsd: Sprague Dawley (SD) rats (25 males and 25 females) were obtained from Harlan, Haslett, Michigan and were designated by the supplier to be 6–7 weeks old. The rats were individually housed in suspended stainless steel caging with mesh floors which conform to the size recommendations in the most recent National Institute of Health Guide for the Care and Use of Laboratory Animals. Animal room temperature and relative humidity were 19–22 °C and 30–70 %, respectively, and there was a 12 h light/dark cycle. Animals were allowed to acclimate to the environment for 1 week and were supplied with PMI Lab Diet Purina Certified Rodent Meal #5002 and filtered tap water ad libitum during the acclimation and study periods. All experimental procedures were performed in accordance with the National Institute of Health Guide for the Care and Use of Laboratory Animals (NIH publication number 80–23 revised 1996). This study was performed by Eurofins / Product Safety Laboratories (Dayton, NJ), study #20684, protocol #P712.02 PHY.

2.4 Dose preparation and administration

From the original 50 rats, 40 healthy rats (20 males and 20 females) seven to eight weeks of age, weighing 193–207 g (males) and 150–175 g (females) were randomly assigned (5/sex/group) to each of the test groups and administered Grains of Paradise extract or vehicle control. The dose levels were assigned as low dose (120 mg of extract/kg/day), intermediate dose (450 mg of extract/kg/day) and 1500 mg of extract/kg/day). The dose selection was based on the planned human exposure in the potential nutritional supplement. Individual doses were calculated based on the most recent weekly body weights of each animal. Extract concentrations were adjusted each week to maintain the targeted dose level for each animal (i.e., mg/kg/day) so that all doses were administered at a constant volume of 5 ml/kg. The control animals received the vehicle only at the same volume as the test groups. The test article was administered as a 2.4%, 9.0%, or 30.0% w/v solution in 10% ethanol in corn oil. On each day of dosing, for each concentration, an appropriate amount of the test article was weighed into a 50 ml volumetric flask. To facilitate the mixing process, approximately 5 g of ethanol was added to the flask and vortexed. The mixture was diluted to 50 ml with corn oil and vortexed again. Dose preparations were used within approximately 2 h and maintained on a magnetic stir plate during administration. Each animal was dosed by oral gavage (using a stainless steel ball-tipped gavage needle attached to an appropriate syringe) daily at approximately the same time ± 2 h for 28 consecutive days. The first day of administration was considered day 1 of the study.

2.5 Clinical observations

All animals were observed twice daily for mortality. Cage-side observations were made daily during the study and any abnormal findings recorded. Detailed observations were recorded on day 1 (prior to administration of test article) and weekly thereafter on all animals. These observations were conducted both while handling the animal and with the animal placed in an open field. Observations included, but were not limited to: changes in skin, fur, eyes, and mucous membranes, occurrence of secretions and excretions and autonomic activity (e.g., lacrimation, piloerection, pupil size, unusual respiratory pattern). Changes in gait, posture and response to handling as well as the presence of clonic or tonic movements, stereotypes (e.g., excessive grooming, repetitive circling), or aberrant behavior (e.g., self-mutilation, walking backwards) were also recorded.

2.6 Food consumption and food efficiency

Animals were allowed ad libitum access to food throughout the study. Animals were fasted overnight prior to blood collection on day 1, 15, 29 and prior to terminal sacrifice on day 31. Individual food consumption was measured, adjusting for spillage, and recorded weekly to coincide with body weight measurements. Mean food consumption was calculated for each sex/dose level during each weekly interval and overall testing interval. Mean food efficiency was also calculated for each sex/dose level based on body weight gain and food consumption data.

2.7 Body weight and body weight gain

Individual body weights were recorded twice during the acclimation period, at study initiation (day 1), and weekly thereafter. Mean body weight gains were calculated for each group at each interval and for the overall (days 1–28) testing interval. Animals were also weighed immediately prior to sacrifice (fasted body weight) for calculation of organ to body weight and organ to brain weight ratios.

2.8 Clinical pathology

All animals were fasted overnight prior to each blood collection. Blood samples for hematology (except prothrombin time and partial thromboplastin time) and clinical chemistry from the test and control groups were collected via orbital sinus bleeding under isoflurane anesthesia on study day 29. Fasting blood glucose was measured on days 1, 15, and 29. Blood samples used to determine the prothrombin time and partial thromboplastin time were collected via the inferior vena cava under isofurane anesthesia for all groups at terminal sacrifice. All blood samples were evaluated for quality by visual examination prior to analysis. Upon completion of clinical chemistry, remaining serum samples were pooled for serology. Pooled serum samples from test animals were evaluated for the absence of viruses near the end of the in-life portion of the study. Examinations were made by Haskell Laboratory for Health and Environmental Sciences.

2.9 Necropsy and histopathology

At scheduled sacrifice, all rats were euthanized by exsanguination from the abdominal aorta under isoflurane anesthesia. Isoflurane (5–10ml) was placed on gauze and administered to the rats enclosed in a bell jar. The animals were placed on the perforated surface above the gauze so they were never in contact with the liquid. The animals were monitored until anesthetized by checking for the absence of reflexes (pain response to pinch test) and that respiration was even and unlabored. Blood collection was performed via the vena cava. Once this procedure was done the exsanguination was performed. All rats were sacrificed on day 31. Gross necropsy included an initial examination of external surfaces and orifices, as well as the cranial, thoracic and abdominal cavities and their contents. Rats were examined for gross lesions. Tissues of interest and any gross lesions were retained in neutral buffered 10% formalin (NBF).

The liver, kidneys, adrenals, brain, heart, thymus, spleen, uterus, ovaries, testes, and epididymides (of all animals sacrificed by design) were weighed wet as soon as possible after dissection to avoid drying. The following organs and tissues from all animals were preserved in NBF for possible future histopathological examination: all gross lesions, lungs, trachea, brain- including sections of the medulla/pons, cerebellar cortex and cerebral cortex, spinal cord (3 levels: cervical, mid-thoracic, and lumbar), thymus, heart, sternum with bone marrow, adrenals, liver, spleen, kidneys, thyroid/parathyroid, ovaries, testes, uterus (with attached urinary bladder, cervix and vagina), esophagus, ileum, cecum, accessory genital organs (epididymides, prostate, and seminal vesicles), peripheral nerve (sciatic), stomach, duodenum, jejunum, colon, rectum, representative lymph node (mesenteric and mandibular), and pancreas and salivary glands. Histological examination was performed on the preserved organs and tissues of the animals from the control groups and test high dose groups. The fixed tissues were trimmed, processed, embedded in paraffin, sectioned, placed on glass microscope slides, and stained with hematoxylin and eosin. Slide preparation and histopathological assessments were performed by Histo-Scientific Research Laboratories.

2.10 Statistics

Mean and standard errors were calculated for all quantitative data. Treated and control groups were compared using a one-way analysis of variance (ANOVA), followed by comparison of the treated groups to control by Dunnett’s t-test for multiple comparisons. A 95% confidence level was used to determine statistically significant differences between treated and control groups.

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3. Results

3.1 Major compounds in the extract

Analysis of the extract by LC-MS revealed three major peaks. The peaks in the HPLC chromatogram (Fig.1) matched the UV spectra and mass fragmentation patterns of previously reported gingerols (Connell, 1970). They are putatively identified as 6-gingerol, 6-shogaol and 6-paradol. These compounds make up the bulk of extract and were most likely responsible for the biological activity. The most abundant were putatively identified as [6]-gingerol (19.5 % of the total extract), [6]-shogaol (12.5 % of the total extract) and [6]-paradol (30.5 % of the total extract; calculated as a percentage relative to the total peak area at 254 nm).

Fig. 1

HPLC chromatogram of Grains of Paradise extract showing major compounds present: 1: 6-gingerol; 2: 6-shogaol 3: 6-paradol.

3.2 Clinical signs

There were no extract related mortalities, however one female (1500 group) and one male (control group) died on test days 5 and 7, respectively, as the result of an intubation error. Additionally, one female (120 group) died on test day 29 during orbital sinus bleeding. Transient clinical signs, most prevalent in the 1500 groups, included soft feces (5/5 males; 2/5 females), facial staining (1/5 males; 4/5 females), ocular and oral discharge (1/5 females), and uro-genital staining (1/5 males; 3/5 females). In addition, one male of the low dose group had red discharge of the penis on test day 3.

3.3 Body weights and food consumption

Overall (days 1 to 28) body weight, mean daily body weight gain, mean daily food consumption, and daily food efficiency for male and female rats at 120, 450 and 1500 mg/kg/day were comparable with control values.

3.4 Clinical pathology

Red cell mass parameters (red blood cell, hemoglobin, hematocrit) were decreased at test day 29 in male rats dosed with 120, 450 or 1500 mg/kg/day (variable statistical significance; means were 90 to 98% of the respective control group means), however the changes were not dose-dependant (Table 1). Red cell distribution width was increased at test day 29 in male and female rats dosed with 1500 mg/kg/day. Although statistically significant, this increase was not associated with any change in related red cell parameters (reticulocyte counts, mean corpuscular volume or microscopic findings). Prothrombin time was minimally shortened at test day 31 in female rats dosed with 450 or 1500 mg/kg/day (means were 94% and 92% of the control group mean, respectively). This change was considered treatment-related, however, minimally shortened coagulation times have no toxicological significance. Prothrombin time and activated partial thromboplastin time on test day 31 in males dosed with 450 mg/kg/day were increased; however, this increase was not dose-dependant.

Table 1

Clinical pathology parameters

There were some treatment-related changes in the clinical chemistry parameters in male and female rats (Table 1). The liver enzyme alkaline phosphatase was mildly increased on test day 29 in male and female rats dosed with 1500 mg/kg/day (means were 207% and 186% of the respective control group means, p≤ 0.05). Aspartate aminotransferase was also elevated in male rats in the 450 and 1500 groups, although the changes were not statistically significant.

Glucose was decreased on test days 15 and 29 in male rats dosed with 450 or 1500 mg/kg/day (Table 1). This minimal decrease in glucose is considered to be treatment related as it intensified with dose and prolonged treatment. In contrast, there were no statistically significant changes in glucose in female rats at any dose tested.

Inorganic phosphorous was increased in male rats dosed with 450 or 1500 mg/kg/day (means were 110% and 117% of the control group mean, respectively). Total protein and globulin were increased on test day 29 in female rats dosed with 1500 mg/kg/day (means were 108, and 110% of the respective control group means) but total protein, albumin, and globulin were decreased on test day 29 in males dosed with 120 mg/kg/day. These findings appear to be treatment related in the females, since it only occurred in the 1500 group, however there was no dose relationship in the males.

3.5 Necropsy and histopathology

No gross abnormalities of toxicological significance were noted for any of the euthanized animals during necropsies at the conclusion of the 30-day observation period. In the male (control group) and female (1500 group) that died as a result of intubation error, the thoracic and cervical findings were histomorphologically consistent with acute purulent inflammation secondary to gavage trauma.

Absolute and relative weights for all organs were comparable to controls in both male and female treated animals, with the notable exception of liver weights. There was a dose dependent increase in mean absolute and relative liver weights in both the male and female test animals compared with the control (Fig. 2). Relative liver weights refer to the ratio of liver weight to body weight. Both the absolute and relative liver weights are significantly (p≤ 0.05) increased in the 450 and 1500 group females. In the 450 and 1500 group males, only the relative liver weights were significantly different from control (p≤ 0.05). These findings did not correlate with any histomorphological changes in the livers of any of the test animals, such as cirrhosis, or steatosis.

Fig. 2

Relative liver weights for male and female rats treated for 28 days with 0, 120, 450, or 1500 mg/kg Grains of Paradise extract (n = 5 per group, bars are mean ± SE); *, p≤ 0.05 compared to control (ANOVA).

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4.0 Discussion

This study has demonstrated that a Grains of Paradise extract rich in 6-gingerol, 6-shogaol and 6-paradol is capable of decreasing blood glucose, but at higher doses may cause liver toxicity. Beyond liver enlargement and elevation in alkaline phosphatase, there were few dose-related changes of toxicological significance. Clinical signs were essentially normal except for the facial and ocular staining in the high dose groups, which was likely due to porphyrin staining from the Harderian gland. Along with the soft feces, these symptoms suggest heightened stress levels or ill health. Although the symptoms were likely treatment related, most of the animals recovered to active and healthy status, with normal feces and no staining, by the end of the study (5/5 males; 3/4 females).

Overall, hematology did not reveal any dose-dependant changes that were of toxicological significance. These results are supported by a study evaluating the safety of a similar ginger extract rich in gingerols and shogaols, which found no significant effect on blood coagulation, blood pressure, or heart rate (Weidner and Sigwart, 2000).

Clinical chemistry revealed decreased blood glucose in the male 450 and 1500 groups, but not in the female groups. Previous studies (Akhani et al., 2004; Al-Amin et al., 2006) showed that gingerol extracts lower blood glucose in male streptozotocin-induced diabetic rats. One study that used both sexes of streptozotocin-induced diabetic rats showed a decrease in blood glucose using a ginger extract (200 mg/kg) however data between the sexes was not distinguished. Further studies are necessary to evaluate the different hypoglycemic effects of gingerol extracts on male verses female rats.

Clinical chemistry also revealed elevated liver enzymes which are toxicologically significant. Increases in alkaline phosphatase or aspartate aminotransferase may occur secondary to induction by a xenobiotic or in association with cholestasis. In this study there was no evidence of cholestasis, i.e., no increase in bilirubin, but absolute and relative liver weights were increased, suggesting early stages of liver damage. Gingerols and related compounds appear to be metabolized by enzymes in the liver (Nakazawa and Ohsawa, 2002; Naora et al., 1992). Liver toxicity has been reported for some herbal extracts including Kava (Piper methysticum G. Forst), Chaparral (Larrea tridentate (DC) Coville), Mistletoe (Phoradendron flavescens (Pursh) Nutt.), Germander (Teucrium chamaedrys Linnaeus), and Comfrey (Symphytum officinale Linnaeus) (Dasgupta, 2003), but a literature search revealed no reports of plant extracts containing gingerols causing liver enlargement or toxicity. In fact, several studies showed a protective effect of gingerols on the liver, with lowered liver enzymes (Hikino et al., 1985; Nie et al., 2006; Yemitan and Izegbu, 2006). Therefore, the liver enlargement and corresponding elevation in alkaline phosphatase observed at high doses (450, 1500 mg/kg) are likely a result of the inability of the liver to metabolize the large amount of gingerols and similar compounds present in high doses of the Grains of Paradise extract.

In conclusion, this 28-day toxicology study in rats showed that a Grains of Paradise extract rich in gingerols may be effective in lowering blood glucose, and is worth investigating as a therapy for diabetes. However, the dose-dependant liver enlargement and elevation in alkaline phosphatase observed in the present study suggest liver toxicity should be considered when administering high doses of Grains of Paradise extract. Further studies would be necessary to determine if other plant extracts that are high in gingerols produce the same effects on the liver when administered at high doses for 28 days.

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Acknowledgements

Partially supported by Phytomedics Inc; Fogarty International Center of the NIH under U01 TW006674 for the International Cooperative Biodiversity Groups; and Rutgers University & NJ Agricultural Experiment Station.

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Footnotes

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