Anemia / 2012 / Article

Review Article | Open Access

Volume 2012 |Article ID 607436 |

Sunday J. Ameh, Florence D. Tarfa, Benjamin U. Ebeshi, "Traditional Herbal Management of Sickle Cell Anemia: Lessons from Nigeria", Anemia, vol. 2012, Article ID 607436, 9 pages, 2012.

Traditional Herbal Management of Sickle Cell Anemia: Lessons from Nigeria

Academic Editor: Aurelio Maggio
Received06 Mar 2012
Revised08 Aug 2012
Accepted09 Aug 2012
Published08 Nov 2012


Background. Patients in West Africa where sickle cell anemia (SCA) is endemic have for ages been treated with natural products, especially herbs, as, is still the case in rural communities. Objective. In this paper we look closely at some of these herbs to see if there are any lessons to be learnt or clues to be found for optimizing the treatments based on them, as had been done in the case of NIPRISAN, which was developed from herbs in Nigeria based on Yoruba Medicine. Methods. Select publications on SCA, its molecular biology and pathology, and actual and experimental cases of herbal treatment were perused in search of molecular clues that can be linked to chemical constituents of the herbs involved. Results. The study revealed that during the last 2-3 decades, much progress was made in several aspects of SCA pharmacology, especially the approval of hydroxyurea. As for SCA herbalism, this paper revealed that antisickling herbs abound in West Africa and that the most promising may yet be found. Three new antisickling herbs (Entandrophragma utile, Chenopodium ambrosioides, and Petiveria alliacea) were reported in May 2011. At NIPRD, where NIPRISAN was developed, three other recipes are currently awaiting development. Conclusion. The study raised the hope that the search in the Tropics for more effective herbal recipes for managing sickle cell anaemia will be more fruitful with time and effort.

1. Introduction

1.1. Health and Disease as Conceived among Communities in Nigeria

Health and disease concepts in African Traditional Medicine are far more advanced than many biomedical scientists would imagine. For instance, long before Ronald Ross revealed mosquito as the vector of malaria and Charles Laveran plasmodium as the parasite [1], communities in tropical African had associated mosquitoes with high fever. Among the Idoma of Benue State, Nigeria, it was known since antiquity that “idapo” (malarial fever) is caused by “imu” (mosquito) and that “ofe-egbe” (dysentery) is caused by bad water or eki-iju (egg of green house flies: a variety of Musca domestica associated with poor sanitation). On the other hand, disorders underlain by more remote causes are attributed to evil spirits and practices frowned upon or forbidden by tradition. Such practices include marriage between close relatives. In Idomaland, marriage even between second cousins is expressly forbidden—it is considered an abomination and a cause of abnormalities or incurable disorders. We are not aware of any specific name for sickle cell disorder in Idoma, but we know that the condition is common and is classed among diseases believed to be caused by evil spirits or misconduct. Ibrahim Muazzam, NIPRD’s ethnobotanist and an associate of Etkin [2], informed us that among the Hausa-Fulani of northern Nigeria, where sickle cell anemia is called “sankara-miji,” the disorder is perceived to be “paranormal” and incurable. Among the Yoruba and Igbo of southern Nigeria, “Abiku” [3] and “ogbanje” [4] or “iyi-uwa” [5] are umbrella terms that include sickle cell anemia and are believed to be “paranormal”. The foregoing suggests to us that traditional communities in Nigeria are not only aware of the syndrome called “sickle cell anemia” but also well aware of its chronicity, endemicity, and “paranormality.” The general manifestations of SCA and strategies for management including herbal treatment are indicated in Figure 1.

1.2. Traditional Herbal Approaches to Sickle Cell Anemia in Nigeria

As described elsewhere [14, 16, 17], among the Efik and Ibibio, Hausa, Igbo, Idoma, and Yoruba: clove (Eugenia caryophyllata or “kanunfari” in Hausa; Piper guineense (“eche” in Idoma or “akwa-ose” in Igbo); grains of paradise (Aframomum melegueta or “otuta” in Idoma); Sorghum bicolor (the leaf stalk yields an extract that looks like blood); Pterocarpus osun (common in the Yoruba state of Osun) are used in various health conditions, including sickle cell anemia. As stated earlier [14] E. caryophyllata, P. guineense, P. osun, and S. bicolor are the herbal components of the Yoruba recipe upon which the antisickling drug Niprisan is based. Prior to the era of Niprisan these herbs were either extracted with “ogoro” (ethanolic distillate of palm wine) or with an aqueous solution trona (sodium sesquicarbonate—a mineral used in Nigeria as tenderizer). Niprisan has passed phases IIA and IIB, and is widely used in Nigeria, and is known or popular in India and the USA. In 2010, Swift [18] of COSMID Corporation, USA, stated the following:A dried extract of four plants has been used to treat patients with SCD in Nigeria for many years (NIPRISAN). It has been through multiple clinical trials in Nigeria and has been formally approved for use in that country since 2006 for the treatment of SCD. The US FDA has determined there is sufficient safety and efficacy data for NIPRISAN to start a Phase III clinical trial. The US FDA Botanical Review Team (BRT) suggested a simpler formulation of NIPRISAN, development of a chemical fingerprint for the formulation using LC/MS and elucidation of some of the anti-sickling compounds in the formulation would improve standardization and increase the probability of obtaining FDA marketing approval.

To the best of our knowledge phase III trial of Niprisan is yet to be reported. We did however suggest in 2011 that phytocannabinoids and vanilloids in E. caryophyllata and P. guineense may account for some of the useful effects of Niprisan in sickle cell crisis [14]. Some of these compounds, including shikimic acid derivatives (vanilloids) and cannabinoids are indicated in Figure 2 and Table 3, respectively.

1.3. An Overview of Vanilloids and Cannabinoids—Agents in Pain Control

The probable roles of vanilloids and cannabinoids receptors in the control of pain, the key issue in sickle cell crisis, are described in a latter section of this paper. In the present we briefly mention these groups of phytochemicals and their synthetic analogues as components of E. caryophyllata and P. guineense, and that they may account for some of the useful effects of Niprisan in sickle cell crisis [14].

1.3.1. Vanilloids

The vanilloids, namely: vanillin, eugenol, zingerone, capsaicin, and piperine (isomer of capsaicin), are molecules with distinctive flavours, yet are quite similar in their molecular structures. All contain a benzene ring. Subtle changes in the sizes or positions of groups of atoms attached to the ring dramatically change their organoleptic and other physicochemical characteristics. Eugenol, capsaicin, and piperine are present in E. caryophyllata and P. guineense. Eugenol has a short hydrocarbon chain attached to the ring, which makes it much less water soluble than vanillin. Although it is practically insoluble in water, it freely mixes with fats and oils. Its fat solubility allows it to penetrate tissues and bind more tightly to lipid rich membrane bound vanilloid receptors. The tail gives eugenol a stronger odour than vanillin. Eugenol has a numbing analgesic effect; because it has some antiseptic effects it is used in the formulation of some brands of toothpaste. It is supposed that the hydrocarbon tail in combination with the polar OH group on the ring allows eugenol to interact with vanilloid receptors in order to produce analgesia and other physiochemical effects. Capsaicin and piperine are of a lower molecular weight than eugenol, and their side chains contain a polar amide group, which makes them less volatile and almost odourless but very “hot”—a persistent burning sensation even at concentrations lower than 10 ppm. The intense flavour results from the molecules’ long hydrocarbon tails. The chain allows them to bind very strongly with their membranous lipoprotein receptors. The fatty tail also allows the molecules to slip through lipid-rich cell membranes, making the burning sensation more pervasive and persistent. Both the burning and analgesic effects of capsaicin or piperine owe to the way the molecules interact their lipoprotein receptors. Paradoxically, the ability of these compounds to cause pain (i.e., the burning sensation) makes them useful in alleviating pain. Exposure to them lowers sensitivity to pain, and it is applied as a counterirritant in the treatment of arthritis and other chronically painful conditions. People who use lots of pepper (as the Idoma and Yoruba do) build up a tolerance to it. According to Fred Senese [19]—“a small jolt of capsaicin excites the nervous system into producing endorphins, which promote a pleasant sense of well-being. The endorphin lift makes spicy foods mildly addictive (and for some, an obsession).”

1.3.2. Cannabinoids

Cannabinoids are a group of terpenophenolic compounds present in Cannabis sativa’ and occur naturally in the nervous and immune systems of animals. The broader definition of cannabinoids refers to a group of substances that are structurally related to tetrahydrocannabinol (THC) or that bind to cannabinoid receptors. The chemical definition encompasses a variety of distinct chemical classes: the classical cannabinoids structurally related to THC; the nonclassical cannabinoids—the aminoalkylindoles, eicosanoids—related to the endocannabinoids 1, quinolines, and arylsulphonamides; additional compounds that do not fall into these standard classes but bind to cannabinoid receptors (CB1 and CB2). An example of such is β-Caryophyllene, which binds selectively to CB2. Currently, there are three general types of cannabinoids: the “phytocannabinoids” that occur uniquely in the cannabis plant or the caryophyllenes that occur in clove; the “endogenous cannabinoids” that are produced in the in humans and other animals; the “synthetic cannabinoids” that are similar compounds produced by in the laboratory by chemical manipulations [20].

1.4. Aim of the Paper

Eleven years into the 21st century, the only cure for SCA is bone marrow transplant that requires a rigorously compatible family member as donor. There is at best only an 85% disease-free survival rate, with a 7% transplant-related mortality rate and a 9% graft failure rate [21]. The procedure is expensive and precarious, and suitable donors are hard to come by. Moreover, patients needing the treatment the most are the least likely to benefit from it due to higher risks. These barriers mean that pharmacologic approaches (and that include herbal palliation) will remain the primary strategy for managing SCA. This paper is necessitated by the mistaken notion that herbal remedies are coming too late in the day to feature significantly in SCA management. We are inclined to reason otherwise and to hold the view that a thorough familiarity with SCA and the ever increasing volume of data on phytochemicals may provide valuable leads, lessons, and clues. In this regard, we here wish to draw attention to the following pertinent comment [22]: Doctors in Nigeria use fagara (F. zanthoxyloides) to reduce the painful crisis of the genetic disease, sickle cell anemia. This herb has a variety of unusual properties that reduce platelet and blood cell sticking. After reading the reports from Nigeria many years ago, I decided to try fagara’s relative prickly ash bark for the same indication. I made a simple tincture of 50% prickly ash bark and 50% ginkgo leaf, and gave it to a young African-American girl in the first grade who constantly missed school and needed to be hospitalized 3-4 times per year due to the painful sickle cell crisis. I gave her about 25 drops three times a day. She immediately stopped having serious problems, her thinking was no longer fuzzy, the frequency of her attacks went down to about one per year, and the severity of the attacks decreased appreciably. This success has continued through the years, as long as she takes her medicine. I saw her last year, and she has blossomed into a beautiful junior high school student, the sickle cell disease now only a bit-player in the background of her life. Another of my patients had lived with the disease his entire life, with almost constant pain, and bimonthly crisis. I gave him 35 drops three times per day, and he immediately improved in the same way as the young girl. This improvement in both frequency of attacks and level of pain has persisted in three of my long-term patients over many years. The wholesale cost of this medicine is less than $20 per month at full dosage. My biggest fear is that this knowledge will be co-opted by a pharmaceutical company, and made available to the many suffering children only at an exorbitant cost.

Elsewhere, we had reasoned on the need for support for clinical trials of promising traditional remedies, and for national drug regulatory agencies in developing countries to show more interest in herbal clinical trials [17]. We attempt in this paper to show how this line of thought should follow from what we have learnt of herbal management of SCA in Nigeria.

2. An Overview of SCA

2.1. Epidemiology of SCA and Some Historical Landmarks

Epidemiology of SCA commenced in the USA in 1910 with the discovery of the disorder in a patient hospitalized in 1904, suffering from anemia [41]. The study progressed through the era involving Pauling and others [42] and Ingram [43, 44]; and is today a success because the necessary preventive measures for SCA are now well known [45]. Also fairly documented is the use in Africa of herbal palliatives for SCA [24, 25, 46]. In this paper we take a closer look at some of these herbs and hypothesize on the likely biochemical bases for their use and how such insight may facilitate their optimization. Ages before European colonization of West Africa, the people had identified a chronic condition variously called “Abiku,” “Ogbanje,” “Sankara-jimi” in Nigeria. Thus, several therapies—herbal and otherwise—waxed and waned, but most of the herbals survived. Shortly after SCA was defined in the US, studies at Ibadan University confirmed the syndrome in Nigeria. During the 1970s studies at Ibadan and Ife described the first series of herbal remedies for SCA. In the 1990s biomedical scientists from Ibadan, Ife, and Zaria developed Niprisan which was launched in 2006. In 2001, before the franchise to produce Niprisan was licensed to a US drug firm, NIPRD had 3 other promising recipes. It should be mentioned that the disease was first named “sickle-cell anemia” in 1922 [47]. But some elements of the disorder had been recognized in an 1846 paper in Southern Journal of Medical Pharmacology which described the absence of a spleen in the autopsy of a runaway slave [48, 49].

2.2. Prevalence, Manifestations, and Management Strategies
2.2.1. Global Prevalence of SCA

Aside from Africa and countries bordering the Mediterranean (e.g., Italy, Greece, Spain, and Turkey) that have high incidences of SCA, significant prevalence has been reported especially in Saudi Arabia, Yemen, India, Pakistan, Bangladesh, and China [6, 23, 26, 50, 51]. The occurrence of SCA in the Americas and in Northwest Europe owes of course to the Triangular Slave Trade [23]. Table 1 shows the general picture of sickle cell disorders (SCDs) worldwide.

Continent/regionMajor disorderRemark/reference

Africa(1) SCA (HbSS)
(2) HbSC
(3) α-Thalassemia
HbC has lysine rather glutamine in 6th position as in β-globin of HbA
One in 12 Blacks worldwide carries the SCA trait. About 1 in 400 has SCA. About 75% of global SCAs are in Africa. About 150,000 SCA cases are born yearly in Nigeria. The carrier frequency ranges between 10% and 40% across equatorial Africa, decreasing to 1-2% in north Africa and <1% in South Africa [6].

Islands and countries in Mediterranean area and the Middle East(1) HbSβ 0 or β
(2) -Thalassemia
(3) -Thalassemia
(4) HbCβ 0 or β +  
(5) SCA
These islands and countries including Turkey have significant cases of SCDs and thalassemias. Saudi Arabia has a yearly rate of 3,000 newborns. Qatif City has the highest rate [7, 8].

America—USA(1) SCA
(2) -Thalassemia
(3) HbCβ 0 or β +  
(4) Other SCDs
About 72,000 persons in the US have SCA, mostly African-Americans at the rate of 1 in 500 newborns as against 1 in 1, 200 for Hispanic-American births [23, 24]. In 2004, 83,149 cases of hospitalization were attributed to SCD in the US at a cost of ~$488 million [9].

Asia(1) SCA
(2) α-thalassemia
(3) β-thalassemia
(4) HbCβ 0 or β +  
(5) HbEβ 0 or β +  
HbC has lysine rather glutamine in 26th position as in β-globin of HbA
SCA is significantly prevalent in Bangladesh, China, and other Asian countries. In India the prevalence ranges from 9.4 to 22.2%. Hemoglobin E/thalassemia is common in Cambodia, Thailand, and India. The Maldives has the highest incidence of thalassemias in the world with a carrier rate of 18%. The corresponding figures for Bangladesh, China, India, Malaysia, and Pakistan range 3–8% of the populations [7, 10].

Europe(1) β-thalassemia
(2) α-thalassemia
(3) HbCβ 0 or β +  
(4) HbEβ 0 or β +  
(5) SCA
Aside from well-known cases in Italy, Greece, Portugal and Spain, significant prevalence of SCDs and the thalassemias occur in others. In UK more than 200 babies are born annually with SCD. The highest prevalence of 1 in 2,415 is in France due to immigration from more endemic zones [10].

New SCDs/1000 in select areas:
 Nigeria: ≥19
 Ghana: 10–18.9
 S. Arabia: 5–9.9
 Europe: 0.1
Types of SCD seen:
(1) -thalassemia
(2) -thalassemia
(3) HbCβ 0 or β +  
(4) HbEβ 0 or β +  
(5) SCA
New SCDs/1,000 in selected areas [7, 12, 25, 26]:
 Mexico: 0.1–0.19
 Central America: 1–18.9
 South America: 0.1-4.0
 Southeast Asia: 0.2–18.9
 Oceania: 0.1

α-Thalassemia results froms decreased production of α-globin leading to an excess of β-globin in affected adults or an excess of γ-globin in affected newborns. The excess β-globin form unstable tetramers called Hemoglobin H (or HbH) consisting of 4 β-globin chains that exhibit abnormal oxygen dissociation curves. β-Thalassemias are either of the β 0 type (thalassemia major) or of the β + type (thalassemia intermedia). In the β 0 type-thalassemias there is no production of β-globin; hence it is the severer form of β-thalassemia. In the β + type thalassemia some β-globin is produced, making it in the milder form. In either case, however, there is a relative excess of α chains, but these do not form tetramers; instead, they bind to RBC membranes, producing membrane damage, and at high concentrations they form toxic aggregates that lead to anemia. As indicated in the table thalassemias can coexist with SCDs.
2.2.2. Manifestations of SCA and Strategies for Management

Key manifestations of SCA are indicted in Figure 2 with comments on symptoms treated with pharmacologic agents and nonpharmacologic strategies. Pharmacologic agencies, of course, include herbal preparations such as Niprisan or Ciklavit.

3. Herbal Materials Used in Managing SCA

3.1. Examples of Plants Used in Managing SCA

A summary of the gross effects and the proposed general actions of some of the herbs used in SCA treatment is presented in Table 2.

Herb/referenceProbable general effect/mode of action/phytochemical constituents

Fagara zanthoxyloides  
(root) [27, 28]
Three isomeric divanilloylquinic acids (burkinabin A, burkinabin B, and burkinabin C) were identified as the likely antisickling agents. But some workers have proposed coumarins, vanillic acid, parahydroxybenzoic acid, and paraflurobenzoic acid.

Carica papaya—(unripe fruit or leaf) [2931]Antisickling effects of 87% inhibitory and 74% reversal activities were obtained from the 5-day fermentation of unripe fruit of C. papaya at 2.5 mg per mL of water. Methanol extract had 64% inhibitory and 55% reversal activities while the chloroform extract was inactive. Phenylalanine, tyrosine, and glycine were thought to be responsible.

(bulb) [32]
The basis is unknown, but allicin in garlic, is a potent stimulus of TRPV1 as mentioned in Section 4 (Biochemical Bases for Herbal Management of SCA). Moreover, garlic is used in many infective conditions especially respiratory infections in SCA.

Hymenocardia acidai   
(leaf) [33]
Mpiana et al. [33] related the anti-SCA activities of H. acida to anthocyanins.

Cajanus cajan   
(seed) [34, 35]
Phenylalanine is thought to be the most active principle in Cajanus cajan seed—a component of Ciklavit antisickling phytomedicine, developed in Nigeria by two professors, Ekeke and Shode [34].

Khaya senegalensis   
(stem bark/leaf) [36]
Fall et al. [36] attributed the anti-SCA effects of K. senegalensis to limonoids.

The herbs Niprisan:
(1) S. bicolor   
(2) P. osun  
(3) Clove   
(4) P. guineense  
The bases for the actions of Sorghum bicolor and Pterocarpus osun are unknown, but they are rich in brightly coloured red/orange flavonoids. They probable act as hematonics especially if they contain folic acid or its analogues. Given their blood red colour, the “Doctrine of Signatures” as mentioned elsewhere [16, 17] may have influenced their inclusion by Yoruba sages of old. It had been supposed that the principles in Niprisan that mitigate, palliate, or reduce the frequency of SCA crisis [18] probably reside mainly in clove and P. guineense [14].

Clove is Eugenia caryophyllata, which, like P. guineense, contains principles that impact SCA crisis. Notably, the isomeric divanilloylquinic acids of Fagara zanthoxyloides contain the vanillyl group as do the vanilloids of clove and P. guineense. A discussion of these principles is presented in Section 4.

ConstituentChemistry and pharmacology

607436.table.003aβ-Caryophyllene is a warm constituent of P. guineense, found also in C. sativa and clove. It occurs as a mixture with α-caryophyllene. It has been found to bind selectively to cannabinoid receptor type 2. This is a key finding given the role of this receptor in pain control.

607436.table.003bPiperine and chavicine are geometric isomers responsible for the pungency of P. guineense, constitute ~5–8%, and are used as ethnomedicines.

607436.table.003cCapsaicin is (8-methyl-N-vanillyl-6-nonenamide) a pungent constituent that produces a burning-sensation in all tissues. Capsaicin and related compounds are called capsaicinoids or vanilloids.

607436.table.003dCubebin is tetrahydrodiperonyl-2-furanol. The furanyl and piperonyl (or vanilyl) groups draw attention to the palliate roles of furan and vanilloids in SCD crisis. “Cubebine” is French designation for diethylether extract of P. cubeba.

4. Biochemical Bases for Herbal Management of SCA

4.1. Structure of Hemoglobin in Relation to Antisickling Agents

Hemoglobins exist in two quaternary states—the deoxygenated conformation called Tense or T-state and the oxygenated conformation called Relaxed or R-state. Sickling occurs only in T-state haemoglobin S (HbS) due to its polymerizing tendency. Thus, a key approach to the crisis of sickling lies in finding a means of inhibiting this tendency of T-state HbS or of causing it to revert to the R state. Safo and coworkers [52] had shown that both HbA and HbS possess allosteric sites with which suitable chemical ligands can interact to shift the equilibrium in favor of the R state and have identified several such entities, called allosteric regulators. These regulators in the case of HbS act as antisickling agents—which can be defined as entities that can inhibit or reverse the sequence of pathological processes leading to sickling. Compounds known to possess this type of effect include (i) “alternative aspirins” such as acetyl-3,5-dibromosalicylic acid [53], (ii) furfural derivatives [52], and (iii) a variety of compounds called capsaicinoids or vanilloids that possess a vanilyl functional group, or its approximation as in vanillin or related compounds [54]. These vanilloids include some substituted benzaldehydes [55] and several shikimic acid byproducts. The structures of some of these antisickling entities including the “alternative aspirins” and “vanilloids” are shown Figure 2.

4.2. Physical Pain and Biochemical Bases for Its Amelioration

Physical pain is an unpleasant sensation associated with actual or potential tissue damage and is essential to an organism’s defense and coordination. But, since pain tends to persist beyond its immediate purpose, organisms are equipped with endogenous systems for controlling pain. Such systems are orchestrated by a complex interplay of ion channels and receptors [56].

4.2.1. Ion Channels

Ion channels are pore-forming proteins that act to establish and control voltage gradient across the plasma membrane of cells by allowing the flow of ions across their electrochemical gradient [56]. A special group called transient receptor potential (or TRP) channels has 28 members that differ in the way they are activated. Some are constitutively open, while others are gated by voltage, ligands, pH, redox state, osmolarity, heat, or mechanical stretch [15].

4.2.2. Vanilloid or Capsaicin Receptor (TRPV1) as an Ion Channel

The so-called transient receptor potential vanilloid (TRPV) group of channels has 6 subfamilies, designated-TRPV1 to TRPV6 [15, 5759]. Caterina et al. [60] indicate that TRPVs are so sensitive to temperature that they are regarded as molecular thermometers. TRPV1 is activated at 43°C and by acidic pH, allicin in garlic, vanilloids (e.g., piperine and capsaicin) and by endocannabinoids (e.g., anandamide and N-arachidonoyl-dopamine). To illustrate how the vanilloids act, it has been shown that capsaicin selectively binds to TRPV1 on the membrane of pain or heat sensing neurons [60]. As a heat activated calcium channel, TRPV1 normally opens at 37–45°C. However, when capsaicin binds to TRPV1, it causes the channel to open below 37°C (body temperature), which is why capsaicin is linked to the sensation of heat. Prolonged activation of these neurons by capsaicin leads to a depletion of presynaptic substance P—a neurotransmitter for pain and heat. Neurons lacking TRPV1 are unaffected by capsaicin [59, 60].

4.2.3. Cannabinoid Receptors in Pain Control

The cannabinoid receptors are a class of cell membrane proteins that are activated by lipids called cannabinoids [61]. Some cannabinoids are endogenous, while others (e.g., the psychoactive constituents of Cannabis sativa) are exogenous. At least two receptor subtypes—CB1 (expressed mainly in the CNS, lungs, liver, and kidneys) and CB2 (expressed in the immune system, hematopoietic cells, and peripheral nerve terminals where they function in pain control)—are known. All these tissues are involved in SCA crisis.

4.2.4. β-Caryophyllene: a Component of P. Guineense and Clove Is a Cannabinoid

β-Caryophyllene, a constituent of Cannabis sativa and of E. caryophyllata and P. guineense: components of Niprisan, has been found to bind selectively to CB2, and to exert significant cannabimimetic effects in mice [62]. This implies that caryophyllene can relief pain in humans and be of benefit to SCD patients. Hence it is possible that Indian hemp, which is richer in caryophyllene than Niprisan, may someday be developed for SCA medication.

5. Conclusion

This paper revealed that antisickling herbs are common in West Africa and that more are still being discovered. At NIPRD, where some aspects of Niprisan are still being researched, there are currently three other recipes earmarked for development. We figure that with time more effective antisickling herbs will be found and developed if proper strategies are instituted.


Niprisan is produced by the Drug Manufacturing Unit of NIPRD as a nonprofit social service authorized by the Nigerian Health Minister after the expiration in 2011 of the license earlier granted Zeechem International Limited. Ciklavit is a product of Neimeth International Pharmaceuticals Plc. It was presented by the Nigerian Health Minister, Professor Eyitayo Lambo, at the 56th session of the World Health Organization regional committee meeting held in Addis Ababa, Ethiopia, in 2006 [63]. The reference to the two products is purely academic, with no conflict of interests whatsoever or any anticipation of financial gain.


  1. F. E. G. Cox, “History of the discovery of the malaria parasites and their vectors,” Parasites & Vectors, vol. 3, article 5, 2010. View at: Publisher Site | Google Scholar
  2. N. Etkin, Edible Medicines: An Ethnopharmacology of Food, University of Arizona Press, 2006.
  3. G. Jones, Dictionary of Mythology Folklore and Symbols, The Scarecrow Press, New York, NY, USA, 1962.
  4. E. Nzewi, “Malevolent ogbanje: recurrent reincarnation or sickle cell disease?” Social Science & Medicine, vol. 52, no. 9, pp. 1403–1416, 2001. View at: Publisher Site | Google Scholar
  5. C. Achebe, Things Fall Apart, William Heinemann limited, London, UK, 1958.
  6. “Sickle-cell anaemia—Report by the Secretariat,” 2006, View at: Google Scholar
  7. W. Jastaniah, “Epidemiology of sickle cell disease in Saudi Arabia,” Annals of Saudi Medicine, vol. 31, no. 3, pp. 289–293, 2011. View at: Publisher Site | Google Scholar
  8. C. Steiner and J. Miller, “Sickle cell disease patients in U.S. hospitals, 2004 Healthcare Cost and Utilization Project (HCUP),” Statistical Brief No. 21, December 2006. Rockville, Md: Agency for Health-care Research and Quality, View at: Google Scholar
  9. N. Awasthy, K. C. Aggarwal, P. C. Goyal, M. S. Prasad, S. Saluja, and M. Sharma, “Sickle cell disease: experience of a tertiary care center in a nonendemic area,” Annals of Tropical Medicine and Public Health, vol. 1, no. 1, pp. 1–4, 2008. View at: Publisher Site | Google Scholar
  10. J. Bardakdjian-Michau, M. Bahuau, D. Hurtrel et al., “Neonatal screening for sickle cell disease in France,” Journal of Clinical Pathology, vol. 62, no. 1, pp. 31–33, 2009. View at: Publisher Site | Google Scholar
  11. “Genes and Human Disease. Genomic Resource Centre”, Health Topic, WHO, Geneva, Switzerland, 2011.
  12. F. B. Piel, A. P. Patil, R. E. Howes et al., “Global distribution of the sickle cell gene and geographical confirmation of the malaria hypothesis,” Nature Communications, vol. 1, no. 8, article 104, 2010. View at: Publisher Site | Google Scholar
  13. A. C. Allison, “The distribution of the sickle-cell trait in East Africa and elsewhere, and its apparent relationship to the incidence of subtertian malaria,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 48, no. 4, pp. 312–318, 1954. View at: Google Scholar
  14. S. J. Ameh, O. O. Obodozie, U. S. Inyang, M. S. Abubakar, and M. Garba, “Climbing black pepper (Piper guineense) seeds as an antisickling remedy,” in Nuts & Seeds in Health and Disease Prevention, V. R. Preedy, R. R. Watson, and V. B. Patel, Eds., pp. 333–343, Academic Press, London, UK, 1st edition, 2011. View at: Google Scholar
  15. D. C. Camerino, D. Tricarico, and J. F. Desaphy, “Ion channel pharmacology,” Neurotherapeutics, vol. 4, no. 2, pp. 184–198, 2007. View at: Publisher Site | Google Scholar
  16. S. J. Ameh, O. O. Obodozie, P. C. Babalola, and K. S. Gamaniel, “Medical herbalism and herbal clinical research—a global perspective,” British Journal of Pharmaceutical Research, vol. 1, no. 4, pp. 99–123, 2011. View at: Google Scholar
  17. S. J. Ameh, O. O. Obodozie, B. A. Chindo, P. C. Babalola, and K. S. Gamaniel, “Herbal clinical trials—historical development and application in the 21st Century,” Pharmacologia, vol. 3, pp. 121–131, 2012. View at: Publisher Site | Google Scholar
  18. R. Swift, “Formulation and standardization of a sickle cell disease drug for clinical trial,” SBIR/ STTR of the United States of America. Agency: department of Health and Human Services, Agency Tracking Number:HL099190, Contact: 1R43HL099190-01, Principal Investigator: Robert Swift. View at: Google Scholar
  19. Fred Senese, “General Chemistry Online. Fire and spices,” View at: Google Scholar
  20. R. Planells-Cases, C. García-Martínez, M. Royo et al., “Small molecules targeting the vanilloid receptor complex as drugs for inflammatory pain,” Drugs of the Future, vol. 28, no. 8, pp. 787–795, 2003. View at: Publisher Site | Google Scholar
  21. R. Iannone, K. Ohene-Frempong, E. J. Fuchs, J. F. Casella, and A. R. Chen, “Bone marrow transplantation for sickle cell anemia: progress and prospects,” Pediatric Blood and Cancer, vol. 44, no. 5, pp. 436–440, 2005. View at: Publisher Site | Google Scholar
  22. “PRICKLY ASH BARK (Zanthoxylum species),” An mhtm document by Dr. Tillotson of Tillotson Institute of Natural Health, 2011. View at: Google Scholar
  23. B. Modell and M. Darlison, Global Epidemiology of Haemoglobin Disorders and Derived Service Indicators, Bulletin of the World Health Organization, WHO, Geneva, Switzerland, 2008.
  24. C. Wambebe, H. Khamofu, J. A. Momoh et al., “Double-blind, placebo-controlled, randomised cross-over clinical trial of NIPRISAN in patients with sickle cell disorder,” Phytomedicine, vol. 8, no. 4, pp. 252–261, 2001. View at: Google Scholar
  25. O. O. Obodozie, S. J. Ameh, E. K. Afolabi et al., “Standardization of the components of Niprisan: a phytomedicine for treating sickle cell disease,” Journal of Medicinal Plants Research, vol. 3, no. 4, pp. 284–289, 2009. View at: Publisher Site | Google Scholar
  26. P. J. Nietert, M. D. Silverstein, and M. R. Abboud, “Sickle cell anaemia: epidemiology and cost of illness,” Pharmacoeconomics, vol. 20, no. 6, pp. 357–366, 2002. View at: Google Scholar
  27. E. A. Sofowora and W. A. Isaacs, “Reversal of sickling and crenation in erythrocytes by the root extract of Fagara zanthoxyloides,” Lloydia, vol. 34, no. 4, pp. 383–385, 1971. View at: Google Scholar
  28. E. A. Sofowora, “Isolation and characterization of an antisickling agent from the root of Fagara zanthoxyloides,” in Proceedings of a Symposium Fagara and the Red Blood Cell, A. Sofowora and A. I. Sodeye, Eds., pp. 79–87, University of Ife Press, Ile-Ife, Nigeria, 1979. View at: Google Scholar
  29. K. D. Thomas and B. Ajani, “Antisickling agent in an extract of unripe pawpaw fruit (Carica papaya),” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 81, no. 3, pp. 510–511, 1987. View at: Google Scholar
  30. C. M. Ogunyemi, A. A. Elujoba, and M. A. Durosimi, “Antisickling properties of Carica papaya Linn,” Journal of Natural Products, vol. 1, pp. 56–66, 2008. View at: Google Scholar
  31. N. O. Imaga, G. O. Gbenle, V. I. Okochi et al., “Antisickling property of Carica papaya leaf extract,” African Journal of Biochemistry Research, vol. 3, no. 4, pp. 102–106, 2009. View at: Google Scholar
  32. S. T. Ohnishi, T. Ohnishi, and G. B. Ogunmola, “Sickle cell anemia: a potential nutritional approach for a molecular disease,” Nutrition, vol. 16, no. 5, pp. 330–338, 2000. View at: Publisher Site | Google Scholar
  33. P. T. Mpiana, V. Mudogo, Y. F. Kabangu et al., “Antisickling activity and thermostability of anthocyanins extract from a congolese plant, Hymenocardia acida Tul. (Hymenocardiaceae),” International Journal of Pharmacology, vol. 5, no. 1, pp. 65–70, 2009. View at: Publisher Site | Google Scholar
  34. G. I. Ekeke and F. O. Shode, “Phenylalanine is the predominant antisickling agent in Cajanus cajan seed extract,” Planta Medica, vol. 56, no. 1, pp. 41–43, 1990. View at: Google Scholar
  35. A. O. Akinsulie, E. O. Temiye, A. S. Akanmu, F. E. A. Lesi, and C. O. Whyte, “Clinical evaluation of extract of Cajanus cajan (Ciklavit) in sickle cell anaemia,” Journal of Tropical Pediatrics, vol. 51, no. 4, pp. 200–205, 2005. View at: Publisher Site | Google Scholar
  36. A. B. Fall, R. Vanhaelen-Fastré, M. Vanhaelen et al., “In vitro antisickling activity of a rearranged limonoid isolated from Khaya senegalensis,” Planta Medica, vol. 65, no. 3, pp. 209–212, 1999. View at: Publisher Site | Google Scholar
  37. C. O. C. Mojisola, E. A. Anthony, and D. M. Alani, “Antisickling properties of the fermented mixture of Carica papaya Linn and Sorghum bicolor (L.) Moench,” African Journal of Pharmacy and Pharmacology, vol. 3, no. 4, pp. 140–143, 2009. View at: Google Scholar
  38. A. A. Awodogan, C. Wambebe, K. Gamaniel, J. Okogun, A. Orisadipe, and P. Akah, “Acute and short-term toxicity of NIPRISAN in rats I: biochemical Study,” Journal of Pharmaceutical Research & Development, vol. 2, pp. 39–45, 1996. View at: Google Scholar
  39. K. Gamaniel, S. Amos, P. Akah et al., “Pharmacological profile of NIPRD 94/002/1-0: a novel herbal antisickling agent,” Journal of Pharmaceutical Research & Development, vol. 3, no. 2, pp. 89–94, 1998. View at: Google Scholar
  40. O. O. Obodozie, S. J. Ameh, E. K. Afolabi et al., “A normative study of the components of niprisan—an herbal medicine for sickle cell anemia,” Journal of Dietary Supplements, vol. 7, no. 1, pp. 21–30, 2010. View at: Publisher Site | Google Scholar
  41. J. Herrick, “Peculiar elongated and sickle-shaped red blood corpuscles in a case of severe anemia,” Archives of Internal Medicine, vol. 6, pp. 517–521, 1910. View at: Google Scholar
  42. L. Pauling, H. A. Itano, S. J. Singer, and I. C. Wells, “Sickle cell anemia, a molecular disease,” Science, vol. 110, no. 2865, pp. 543–548, 1949. View at: Google Scholar
  43. V. M. Ingram, “Gene mutations in human hæmoglobin: the chemical difference between normal and sickle cell hæmoglobin,” Nature, vol. 180, no. 4581, pp. 326–328, 1957. View at: Publisher Site | Google Scholar
  44. V. M. Ingram, “Abnormal human haemoglobins. III the chemical difference between normal and sickle cell haemoglobins,” Biochimica et Biophysica Acta, vol. 36, no. 2, pp. 402–411, 1959. View at: Google Scholar
  45. A. Gabriel and J. Przybylski, “Sickle-cell anemia: a look at global haplotype distribution,” Nature Education, vol. 3, no. 3, pp. 2–12, 2010. View at: Google Scholar
  46. J. Okpuzor, O. Adebesin, H. Ogbunugafor, and I. Amadi, “The potential of medicinal plants in sickle cell disease control: a review,” International Journal of Biomedical and Health Sciences, vol. 4, no. 2, pp. 47–55, 2008. View at: Google Scholar
  47. V. R. Mason, “Sickle cell anemia,” Journal of the American Medical Association, vol. 79, no. 14, pp. 1318–1320, 1922. View at: Google Scholar
  48. “Sickle Cell Disease: History And Origin,” The Internet Journal of Haematology 1 (2), 2011, View at: Google Scholar
  49. “From 1918 Autopsy, A First Glimpse of Sickle Cell - and a Warning,” View at: Google Scholar
  50. D. J. Weatherall and J. B. Clegg, “Inherited haemoglobin disorders: an increasing global health problem,” Bulletin of the World Health Organization, vol. 79, no. 8, pp. 704–712, 2001. View at: Google Scholar
  51. U. A. Ndefo, A. E. Maxwell, H. Nguyen, and T. L. Chiobi, “Pharmacological management of sickle cell disease,” P and T, vol. 33, no. 4, pp. 238–243, 2008. View at: Google Scholar
  52. M. K. Safo, O. Abdulmalik, R. Danso-Danquah et al., “Structural basis for the potent antisickling effect of a novel class of five-membered heterocyclic aldehydic compounds,” Journal of Medicinal Chemistry, vol. 47, no. 19, pp. 4665–4676, 2004. View at: Publisher Site | Google Scholar
  53. J. A. Walder, R. H. Zaugg, R. S. Iwaoka, W. G. Watkin, and I. M. Klotz, “Alternative aspirins as antisickling agents: acetyl-3,5-dibromosalicylic acid,” Proceedings of the National Academy of Sciences of the United States of America, vol. 74, no. 12, pp. 5499–5503, 1977. View at: Google Scholar
  54. D. J. Abraham, A. S. Mehanna, F. C. Wireko, J. Whitney, R. P. Thomas, and E. P. Orringer, “Vanillin, a potential agent for the treatment of sickle cell anemia,” Blood, vol. 77, no. 6, pp. 1334–1341, 1991. View at: Google Scholar
  55. I. N. Nnamani, G. S. Joshi, R. Danso-Danquah et al., “Pyridyl derivatives of benzaldehyde as potential antisickling agents,” Chemistry and Biodiversity, vol. 5, no. 9, pp. 1762–1769, 2008. View at: Publisher Site | Google Scholar
  56. “Ion Channels: structure and function,” 2011, View at: Google Scholar
  57. R. Vennekens, G. Owsianik, and B. Nilius, “Vanilloid transient receptor potential cation channels: an overview,” Current Pharmaceutical Design, vol. 14, no. 1, pp. 18–31, 2008. View at: Publisher Site | Google Scholar
  58. K. Venkatachalam and C. Montell, “TRP channels,” Annual Review of Biochemistry, vol. 76, pp. 387–417, 2007. View at: Publisher Site | Google Scholar
  59. W. Loging, L. Harland, and B. Williams-Jones, “The vanilloid receptor TRPV1: 10 years from channel cloning to antagonist proof-of-concept,” Nature Reviews Drug Discovery, vol. 6, no. 5, pp. 357–372, 2007. View at: Publisher Site | Google Scholar
  60. M. J. Caterina, M. A. Schumacher, M. Tominaga, T. A. Rosen, J. D. Levine, and D. Julius, “The capsaicin receptor: a heat-activated ion channel in the pain pathway,” Nature, vol. 389, no. 6653, pp. 816–824, 1997. View at: Publisher Site | Google Scholar
  61. E. S. Graham, J. C. Ashton, and M. Glass, “Cannabinoid receptors: a brief history and ‘what's hot’,” Frontiers in Bioscience, vol. 14, no. 3, pp. 944–957, 2009. View at: Publisher Site | Google Scholar
  62. J. Gertsch, M. Leonti, S. Raduner et al., “Beta-caryophyllene is a dietary cannabinoid,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 26, pp. 9099–9104, 2008. View at: Publisher Site | Google Scholar
  63. W. Eya, Nigeria: Sickle Cell—Lambo Presents Ciklavit at WHO, Daily Champion, Lagos, Nigeria, 4th edition, 2006.

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