Научная статья на тему 'Comparative haematological and biochemical effects of cocktail vaccine (DHLPPi) and Abrus precatorius seed aqueous extract on canine Parvoviral vaccinated and unvaccinated Nigerian local dogs'

Comparative haematological and biochemical effects of cocktail vaccine (DHLPPi) and Abrus precatorius seed aqueous extract on canine Parvoviral vaccinated and unvaccinated Nigerian local dogs Текст научной статьи по специальности «Фундаментальная медицина»

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Ключевые слова
ABRUS PRECATORIUS / VACCINE / IMMUNOINHIBITION / CANINE PARVOVIRUS / ВАКЦИНА / іМУНОіНГіТАЦіЯ / ПАРВОВіРУС СОБАК

Аннотация научной статьи по фундаментальной медицине, автор научной работы — Tion M.T., Fotina H.A., Saganuwan A.S.

Because of increasing incidence of resistance to infectious microorganisms, immunotherapy has been considered as an alternative/complementary to chemotherapy. More so Abrus precatorius leaf extract has been reported to have immunomodulatory effects in animals. In view of this, comparative haematology and biochemistry of cocktail vaccine (DHLPPi) and Abrus precatorius seed extract (APSE) was studied in rats. Sixteen (16) Nigerian local dogs of both sexes weighing 7.19 ± 0.46 kg, aged 15.44 ± 0.76 weeks old were divided into four groups of 4 each. Group 1, 2, 3 and 4 was administered 1 ml of normal saline (0.9%), APSE (2.72 mg/Kg), APSE (2.72 mg/Kg)+DHLPPi (1 ml) and DHLPPi (1 ml) respectively. Fourteen days after administration of the extract and vaccine, 3 ml of blood sample was collected from each of the dogs for haematology and serum biochemistry. The findings revealed significantly (P < 0.05)decreased packed cell volume, haemoglobin, erythrocytes, neutrophils, leucocytes, platelets and increased monocytes, decreased total protein, albumin, globulin, albumin/globulin ratio, alkaline phosphatase, alanine aminotransferase and aspartate aminotransferase in the group administered extract and extract/vaccine. Hence, the extract and extract/DHLPPi vaccine can be used in prevention chronic viral infection of dogs.

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Текст научной работы на тему «Comparative haematological and biochemical effects of cocktail vaccine (DHLPPi) and Abrus precatorius seed aqueous extract on canine Parvoviral vaccinated and unvaccinated Nigerian local dogs»

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Scientific Messenger of Lviv National University of Veterinary Medicine and Biotechnologies

ISSN 2518-7554 print doi: 10.32718/nvlvet9215

ISSN 2518-1327 online http://nvlvet.com.ua

UDC 619:57.083:636.7

Comparative Haematological and Biochemical Effects of Cocktail Vaccine (DHLPPi) and Abrus precatorius Seed Aqueous Extract on Canine Parvoviral Vaccinated and Unvaccinated Nigerian Local Dogs

M.T. Tion1, H.A. Fotina2, A.S. Saganuwan1

1College of Veterinary Medicine, University of Agriculture, Makurdi, Nigeria 2Sumy National Agrarian University, Sumy, Ukraine

Tion, M.T., Fotina, H.A., & Saganuwan, A.S. (2018). Comparative Haematological and Biochemical Effects of Cocktail Vaccine (DHLPPi) and Abrus precatorius Seed Aqueous Extract on Canine Parvoviral Vaccinated and Unvaccinated Nigerian Local Dogs. Scientific Messenger of Lviv National University of Veterinary Medicine and Biotechnologies, 20(92), 73-78. doi: 10.32718/nvlvet9215

Because of increasing incidence of resistance to infectious microorganisms, immunotherapy has been considered as an alternative/complementary to chemotherapy. More so Abrus precatorius leaf extract has been reported to have immunomodulatory effects in animals. In view of this, comparative haematology and biochemistry of cocktail vaccine (DHLPPi) and Abrus precatorius seed extract (APSE) was studied in rats. Sixteen (16) Nigerian local dogs of both sexes weighing 7.19 ± 0.46 kg, aged 15.44 ± 0.76 weeks old were divided into four groups of 4 each. Group 1, 2, 3 and 4 was administered 1 ml of normal saline (0.9%), APSE (2.72 mg/Kg), APSE (2.72 mg/Kg)+DHLPPi (1 ml) and DHLPPi (1 ml) respectively. Fourteen days after administration of the extract and vaccine, 3 ml of blood sample was collected from each of the dogs for haematology and serum biochemistry. The findings revealed siggnificantly (P < 0.05)decreasedpacked cell volume, haemoglobin, erythrocytes, neutrophils, leucocytes, platelets and increased monocytes, decreased total protein, albumin, globulin, albumin/globulin ratio, alkaline phosphatase, alanine aminotransferase and aspartate aminotransferase in the group administered extract and extract/vaccine. Hence, the extract and extract/DHLPPi vaccine can be used in prevention chronic viral infection of dogs.

Key words: Abrus precatorius, Vaccine, Immunoinhibition, Canine parvovirus.

nopiBMHM гематолопчних та 6ioxiMi4H^ показникчв собак при застосуванш вакцини (DHLPPi) та водного екстракту насшня Abrus precatori

M.T. TioH1, Г А. Фотша2, А.С. Сагануван1

1Коледж ветеринарног медицини, Сшъскогосподарсъкий утверситет, Mampdi, Нiгерiя 2Сумський нацюнальний аграрний унiверситет, м. Суми, Украти

З давтх ча&в лтарсът рослини використовувалися при л^вант та за для контроля захворювань людини та тварин. Деят рослини впливаютъ на гематологiчнi та бюхмчш показники сироватки кровi. Також кнуютъ вiдомостi що деят сучасш про-тивiруснi препарати е неспецифiчними для конкретних вiрусiв. Тому розробка нових економiчно ефективних i специфiчних про-тивiрусних схем е доситъ актуалъним а також першочерговим завданням сучасних до^дженъ. Через зростання випадмв стш-костi до тфекцшних мiкроорганiзмiв, iмунотерапiя розглядаетъся як алътернатива хтютерапи. Бшъш того, екстракт листя Abrus precatori, як повiдомляетъся, мае iмуномодулюючу дт у тварин. З огляду на це, нами були проведем до^дження на щурах по визначенню проведенню порiвнялъноi гематологiчноi та бюхтачног оцтки сироватки кровi тсля застосування асоцтованог вакцини (DHLPPi) та екстракту з настня Abrus precatori (APSE). Також для дослiдiв використовували ш^тнадцятъ (16) тгертсъких мкцевих собак обох статей вагою 7,19 ± 0,46 кг, втом 15,44 ± 0,76 тижшв. Тварин було роздтено на чотири групи по 4 у кожнш. Групам 1, 2, 3 i 4 вводили вiдповiдно 1мл фiзiологiчного розчину (0,9%), APSE (2,72 мг/кг), APSE (2,72 мг/кг) + DHLPPi (1 мл) та DHLPPi (1 мл) вiдповiдно. Через чотирнадцятъ дтв тсля введення екстракту та вакцини вiд кожног собаки вiдбирали 3 мл кровi для до^дження гематологiчних та бiохiмiчних показнитв сироватки кровi. В резулътатi проведених до^дженъ вста-

Article info

Received 18.10.2018 Received in revised form 16.11.2018 Accepted 19.11.2018

College of Veterinary Medicine University of Agriculture, Makurdi P.M.B 2373, Makurdi, Benue State, Nigeria.

Tel.: +234-803-723-98-72

+234-705-859-89-93

E-mail: tions_doc@yahoo.co.uk

Sumy National Agrarian University, Gerasim Kondratyev Str., 160, Sumy, 40000, Ukraine.

повили що застосування вакцини та екстракту мае високу ефективтсть у профтактищ вiрусних захворювань собак. В до^дних группах де проводили комплексне застосування екстракту разом з DHLPPi ефективтсть профилактики вiрусних захворювань набагато вище.

Ключовi слова: Abrusprecatorius, вакцина, 1мунотг1тащя, парвовiрус собак.

Introduction

Since ancient times, medicinal plants have been used in the treatment and control of human and livestock diseases and herbal remedies represent the source of one in every four drugs (Garg, 2006). Some plants have effects on hematology and serum biochemistry (Jiang et al., 2015). Viral infections are known as one group of the major causes of death worldwide (Adelowotan et al.,

2008). Some antiviral drugs are nonspecific for particular viruses (Bhutia et al., 2009). The development of novel cost-effective and specific antiviral regimens is the prime focus of the current medical research (Adedapo et al., 2007). The plant-related drugs have activities against viral infections (Anam, 2001).

Some medicinal plants used in the treatment of viral diseases in animals include Acacia nilotica, Gardenia erubescens (Ganesan and Bhatt, 2008), Vigna unguiculata (Guyton and Hall, 2007), Englerina gabonensis subsp gabonensis and Globimatula globiferus var letuzeyi used the treatment of FMD cattle. While Epiphyllum truncata (Sacks, 2009), Parkia filicolidea (Cooper, 2004), Cannabis indica (Omage et al., 2015), Lugenaria vulgeris, Khaya senegalensis, and Datura metel are used in the treatment of Newcastle disease in chicken.

Abrus precatorius Linn is used to cure fever, stomatitis, bronchitis, asthma and diabetes (Newman and Cragg, 2007), chronic nephritis (Saganuwan, 2009), cancer (Saganuwan, 2011), sores, scratches, wounds, leucoderma, tetanus, boils, abscesses, for prevention of rabies (Sacks,

2009), with haematonic and plasma expander effect (Saganuwan, 2010). A. precatorius extracts induce apoptosis on various types of cancers (Garg, 2006). The plant has antitumoral (Ramnath et al., 2002), mitogenic (Saganuwan and Gulumbe, 2005b), antifertility (Saganuwan, 2009), immunopotentiating (Ligha et al., 2009), antimicrobial (Newman and Cragg, 2007), immunostimulant (Saganuwan, 2009), antianaphylactic (Sacks, 2009), and anti-inflammatory activities. The present study was undertaken to evaluate the effects of aqueous seed extract of Abrus precatorius and DHLPPi vaccine on haematological and biochemical parameters of unvaccinated and vaccinated Nigerian local dogs.

Materials and methods

Collection of Plant material. The plant materials (seeds) used for the study were collected from Kwande Local Government Areas of Benue State, Nigeria between the months of September and November and identified by a botanist in the Department of Biological Science, University of Agriculture, Makurdi where a voucher with voucher number (11) specimen was deposited.

Preparation of Extract. The seeds were thoroughly washed with tap water, dried on filter papers and air dried under open shade for 1 month. The seeds were pulverized

with the help of a mortar and pestle to coarse powder and finally ground into fine powder using a grinding machine. Fifty grammes (50 gm) of Abrus precatorius seed powder was dissolved in four hundred and fifty milliliter (450 mL) of aqueous extract in a conical flask. The mixture was shaken intermittently throughout a whole day using glass rod stirrer and allowed to stand overnight. The mixture was separately filtered with Whatman filter paper No. 1 into measuring cylinder and concentrated at 60oC in an incubator and stored in a refrigerator at 4 oC until required for use (Sacks, 2009).

Administration of Abrus Precatorius seed extract and vaccine. The method of Yamba was used for selection of extract doses used for haematology and serum biochemistry. Median lethal dose (LD50) of 187.5 mg/Kg body weight of the extract was extrapolated to dogs (2.72 mg/Kg) using Human Equivalent Dose (HED) formula. The extract was prepared as 0.5% solution and administered orally to all the dogs before feeding, for a period of fourteen (14) days. The dogs were divided into four groups of 4 each. Group 1 served as the control and received normal saline, group 2 received the 2.72 mg/Kg aqueous extract alone and group 3 dogs were vaccinated against canine parvovirus infection using DHLPPi in addition to 2.72 mg/Kg of the extract whereas group 4 dogs were vaccinated with DHLPP vaccine only. Blood sample (3 ml) was obtained before and after the treatment from the cephalic vein with the help of 21 gauge needle and 10mL syringe for the determination of hematological and biochemical parameters.

Haematological Parameters. Haematological parameters were determined according to the method of Cheesbrough. The parameters were red blood cells (RBCs) count, packed cell volume (PCV), haemoglobin concentration (HB), mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH), mean corpuscular haemoglobin concentration (MCHC), white blood cells (WBCs) count and differential white blood cells count (DWBC).

Serum Biochemical Parameters. Serum biochemical parameters were determined. The parameters were total protein, albumin, globulin, albumin/globulin ratio, alkaline phosphatase (ALP) and alanine aminotransferases (ALT), aspartate aminotransferases (AST), potassium, sodium and chloride.

Statistical Analysis. The data on haematological and serum biochemical parameters were expressed as mean ± standard error of mean (SEM). One way analysis of variance (ANOVA) was used to analyze the data on haematological and serum biochemical parameters at 5% level of significance (Saganuwan and Onyeyili, 2010).

Results

The haematological changes observed in dogs administered aqueous seed extract of A. precatorius,

extract and DHLPPi vaccine and DHLPPi vaccine only are presented in Table 1. Dogs administered 2.72 mg/Kg of the extract, 2.72 mg/Kg of the extract + 1 dose of DHLPPi vaccine and 1 dose of DHLPPi vaccine showed significant decrease (P < 0.05) in PCV and HB relative to the control (normal saline 0.9%) and the pretreatment group.

The leucogram showed a statistically significant decrease (P < 0.05) in WBC count and NEU in dogs given 2.72 mg/Kg of extract relative to the control and

pretreatment group. While a significant increase (P < 0.05) was observed for lymphocyte counts in dogs given 2.72 mg/Kg extract, 2.72 mg/Kg extract + DHLPPi and DHLPPi respectively.

A significant decrease (P < 0.05) was seen in MON in dogs given 2.72 mg/Kg extract and 2.72 mg/Kg extract + DHLPPi and EOS in dogs given 2.72 mg/Kg extract + DHLPPi group, while a significant decrease (P < 0.05) was observed in dogs given DHLPPi vaccine group respectively.

Table 1

The effects of aqueous seed extracts of A. precatorius extract and DHLPPi vaccine on haematological parameters of dogs

Parameters Group Normal Saline (0.9%) Extract (2.72 mg/kg) Extract (2.72 mg/kg) + DHLPPi vaccine DHLPPi vaccine

PCV (%) Pretreatment Treatment 36.75 ± 1.49 38.00 ± 1.22 37.00 ±2.12 32.00 ± 1.41b 38.50 ±3.66 32.10 ±0.58b 37.25 ±2.78 31.00 ± 1.73b

HB (g/L) Pretreatment 12.25 ± 0.49 12.30 ±0.71 12.80 ± 1.22 12.43 ±0.92

Treatment 12.65 ± 0.39 10.68 ±0.47b 10.67 ±0.20b 10.30 ±0.58b

RBC (X109/ L) Pretreatment 6.12 ± 0.25 6.16 ±0.35 6.42 ±0.61 6.21 ±0.46

Treatment 6.33 ± 0.20 5.33 ± 0.24b 5.33 ± 0.10b 5.11 ±0.24b

MCV (fL) Pretreatment 60.00 ± 0.00 59.00 ±0.00 59.50 ±0.29 60.00 ±0.00

Treatment 60.00 ± 0.00 60.00 ±0.00 60.00 ±0.00 60.33 ±0.33

MCH (pg) Pretreatment 19.25 ± 0.48 19.25 ± 0.25 19.25 ±0.25 19.00 ±0.41

Treatment 19.22 ± 0.25 19.5 ±0.50 19.00 ±0.58 19.33 ±0.33

MCHC (g/dL) Pretreatment 32.25 ± 0.48 32.5 ± 0.29 32.75 ±0.85 32.00 ±0.58

Treatment 31.75 ± 0.25 32.5 ± 0.50 32.00 ±0.58 32.00 ±0.00

WBC (X109/ L) Pretreatment 10.88 ± 0.56 12.05 ±0.75 9.55 ±0.85 9.65 ± 1.08

Treatment 9.80 ± 1.00 8.85 ± 0.67b 9.41 ± 1.14b 9.67 ±0.75

NEUT (X109/ L) Pretreatment 70.00 ± 3.42 65.25 ±2.43 68.75 ±2.57 67.00 ±3.94

Treatment 70.25 ± 3.66 64.00 ±4.12b 65.67 ±2.03b 67.33 ±3.71

LYM (X109/ L) Pretreatment 21.25 ± 3.07 28.75 ±1.11 27.50 ±2.26 29.75 ± 1.18

Treatment 22.5 ± 2.99 29.50 ± 1.85a 29.33 ± 1.20a 30.33 ±2.85a

MON (X109/ L) Pretreatment 8.00 ± 2.71 5.25 ±1.11 3.50 ±0.87 7.25 ±2.18

Treatment 6.75 ± 2.99 6.00 ± 2.48a 4.67 ± 2.40a 2.00 ± 1.16b

EOS (X109/ L) Pretreatment 0.75 ± 0.75 0.75 ±0.48 0.55 ±0.25 0.50 ±0.29

Treatment 0.50 ± 0.50 0.50 ±0.50 0.50 ±0.00 0.53 ±0.33

BAS (X109/ L) Pretreatment 0.00 ± 0.00 0.00 ±0.00 0.00 ±0.00 0.00 ±0.00

Treatment 0.00 ± 0.00 0.00 ±0.00 0.00 ±0.00 0.00 ±0.00

PLT (X109/ L) Pretreatment 176.8 ± 4.03 174.3 ±2.18 181.50 ± 4.65 192.8 ± 11.69

Treatment 175.3 ± 3.68 172.8 ±2.50b 176.3 ±6.89b 179.3 ± 10.35b

Key: a = significantly higher (P < 0.05) in comparison with the control; b = significantly lower (P < 0.05) in comparison with the control; RBC = Red Blood Cells, HB = Hemoglobin, PCV = Packed Cell Volume, MCV = Mean Corpuscular Volume, MCH = Mean Corpuscular Hemoglobin, MCHC = Mean Corpuscular Hemoglobin Concentration, WBC = White Blood Cells, LYM = Lymphocytes, MON = Monocytes, NEU = Neutrophils, EOSIN = Eosinophils, PLT = Platelets, DHLPPi = Distemper, Hepatitis, Leptospirosis, Parvovirus and Para-influenza vaccine.

Dogs given 2.72 mg/Kg extract + DHLPPi and DHLLPi showed a significant decrease (P < 0.05) in PLT respectively.

The serum biochemical changes observed in dogs administered aqueous seed extract of A. precatorius extract and DHLPPi vaccine and DHLPPi vaccine only are presented in Table 2.

Dogs given 2.72 mg/Kg of the extract, 2.72 mg/Kg of the extract + 1 dose of DHLPPi vaccine and 1 dose of DHLPPi vaccine showed significant decrease (P < 0.05) in total protein respectively. A significant decrease (P < 0.05) in the albumin, the group treated with 2.72 mg/Kg extract + DHLPPi, DHLPPi and extract (2.72 mg/Kg) respectively. Enzyme assay showed a significant decrease (P < 0.05) in ALP of dogs administered 2.72 mg/Kg extract, 2.72 mg/Kg of the

extract + DHLPPi and DHLPPi. There was a significant AST decrease (P < 0.05) in 2.72 mg/Kg extract and 2.72 mg/Kg extract + DHLPPi. A significant decrease (P < 0.05) in ALT was observed in dogs that received extract (2.72 mg/Kg), 2.72 mg/Kg extract + DHLPPi and DHLPPi.

Electrolyte assay showed a significant increase (P < 0.05) in potassium of dogs that received 2.72 mg/Kg extract and 2.72 mg/Kg extract + DHLPPi group, while sodium was significantly decreased (P < 0.05) in DHLPPi group.

Dogs given 2.72 mg/Kg of the extract, 2.72 mg/Kg of the extract + 1 dose of DHLPPi vaccine and 1 dose of DHLPPi vaccine showed significant decrease (P < 0.05) in total protein respectively.

A significant decrease (P < 0.05) in the albumin, the group treated with 2.72 mg/Kg extract + DHLPPi, DHLPPi and extract (2.72 mg/Kg) respectively.

Enzyme assay showed a significant decrease (P < 0.05) in ALP of dogs administered 2.72 mg/Kg extract, 2.72 mg/Kg of the extract + DHLPPi and DHLPPi. There was a significant AST decrease (P < 0.05) in 2.72 mg/Kg extract and 2.72 mg/Kg extract + DHLPPi. A significant

decrease (P < 0.05) in ALT was observed in dogs that received extract (2.72 mg/Kg), 2.72 mg/Kg extract + DHLPPi and DHLPPi. Electrolyte assay showed a significant increase (P < 0.05) in potassium of dogs that received 2.72 mg/Kg extract and 2.72 mg/Kg extract + DHLPPi group, while sodium was significantly decreased (P < 0.05) in DHLPPi group.

Table 2.

The effects of aqueous seed extracts of A. precatorius extract and DHLPPi vaccine on serum biochemical parameters of dogs

Parameters Group Normal Saline Extract (2.72 Extract (2.72 mg/kg) + DHLPPi vaccine

(0.9%) mg/kg) DHLPPi vaccine

Total protein Pretreatment 6.05 ± 0.36 5.58 ±0.33 5.38 ±0.28 5.40 ±0.27

(mg/dL) Treatment 6.25 ± 0.19 4.50 ± 0.60b 4.63 ± 0.68b 4.90 ± 0.66b

Albumin (mg/dL) Pretreatment 3.63 ± 0.67 2.90 ±0.09 2.9 ±0.22 2.85 ±0.30

Treatment 3.60 ± 0.34 2.20 ± 0.38b 2.43 ± 0.38b 2.40 ± 0.72b

Globulin (mg/dL) Pretreatment 2.42 ± 0.31 2.68 ±0.24 2.48 ±0.06 2.55 ±0.03

Treatment 2.45 ± 0.15 2.30 ± 0.22b 2.20 ± 0.30b 2.50 ±0.06

Albumin/Globulin Pretreatment 1.50 ± 0.00 1.08 ±0.00 1.17 ±0.00 0.94 ±0.00

Ratio Treatment 1.47 ± 0.00 0.56 ±0.00 b 0.61 ±0.00b 0.96 ±0.00

ALP (u/L) Pretreatment 61.5 ± 3.86 15.0 ±2.65 17.25 ±1.38 40.0 ± 13.19

Treatment 61.75 ± 3.28 14.5 ± 2.22b 14.0 ± 5.51b 30.67 ± 13.35b

AST (u/L) Pretreatment 12.75 ± 5.23 7.00 ± 1.23 7.50 ±0.87 12.95 ±3.57

Treatment 12.85 ± 5.20 7.75 ± 1.55a 11.67 ± 3.18a 13.03 ±4.98

ALT (u/L) Pretreatment 11.75 ± 2.29 7.25 ±1.60 6.25 ±0.95 6.95 ±1.44

Treatment 11.80 ± 2.52 9.0 ± 1.29a 13.67 ± 3.18a 7.00 ± 1.53

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Potassium (mmol/L) Pretreatment 3.78 ± 0.22 3.05 ±0.49 2.83 ±0.45 3.60 ±0.23

Treatment 3.55 ± 0.22 4.98 ± 1.08a 4.43 ± 1.27a 3.58 ± 1.13

Sodium (mmol/L) Pretreatment 139.3 ± 13.30 167.3 ± 16.9 149.3 ±5.02 130.8 ±9.01

Treatment 134.8 ± 12.50b 107.0 ±4.66b 109.3 ±28.47b 116.3 ±16.84b

Chloride (mmol/L) Pretreatment 106.5 ± 3.66 89.5 ±5.39 117.5 ±4.03 106.0 ±2.80

Treatment 103.3 ± 2.72b 85.75 ±1.65b 109.0 ± 13.32b 89.0 ± 5.57b

Key: a = significantly higher (P < 0.05) in comparison with the control; b = significantly lower (P < 0.05) in comparison with the control; ALP = Alkaline Phosphatase, ALT = Alanine Aminotransferase, AST = Aspartate Aminotransferase DHLPPi = Distemper, Hepatitis, Leptospirosis, Parvovirus and Para-influenza vaccine

Discussion

The significant decrease in PCV, HB and RBC in dogs administered 2.72 mg/Kg extract, 2.72 mg/Kg extract + DHLPPi and DHLPPi show that both the extract and the vaccine could cause hemolysis in Nigerian local dogs. This disagrees with the finding that the extract causes increase in PCV, HB and RBC (Saganuwan and Gulumbe, 2005b). Hence the prolong administration of the seeds to animals may cause anemia. Saganuwan and Onyeyili (2016) and Adedapo et al. (2007) had earlier reported that Abrus precatorius extract could cause haemolysis. The plant's active principle is abrin, a toxalbumin (phytoprotein), which is antigenic and may be responsible for the observed toxic effects (Saganuwan and Ogalue, 2008). Abrin consists of abrus agglutinin (a haemaglutinin), and toxic lectins abrins a-d, the toxic glycoproteins present in the seeds (Sacks, 2009). The leucopenia and neutropenia observed in the present study show that both the plant and the extract have immunoinhibitory effect and as such can be used in the treatment of hyperimmuno stimulatory diseases such as systemic lupus erythematosus, psoriasis and inflammatory bowel disease by causing decreasing immune response (Saganuwan and Gulumbe, 2005a). Lymphocytosis

observed in all the treatment groups showed that the extract and vaccine have immunomodulatory effects. This could be due to stimulation of humoral system (Ligha et al., 2009). Although, vaccine induced immunosuppression had been reported in humans (Omage et al., 2015), polyvalent canine vaccines cause significant lymphopenia to mitogen about 3-11 days after vaccination. By day 14 post vaccination, the lymphocytopenia changes lymphocytosis (Saganuwan and Onyeyili, 2016) which is beneficial during immune response.

The observed lymphocytosis could be effect of the active components of the extract and vaccine on the body defense mechanism (Saganuwan and Gulumbe, 2005b). Selective enhancement of the immune response is a primary goal in prevention of diseases. Drugs and chemicals have been known to induce lymphocytosis in man and animals (Sacks, 2009).

The monocytosis observed in the present study disagrees with the report of Saganuwan et al. (2014) indicating that Abrus precatorius extract caused monocytopenia. The cause of immune-stimulatory/inhibitory potential of the A. precatorius seed extract may be unknown. Hypoproteinaemia, hypoalbuminaemia observed in all the groups and low albumin-globulin ratio seen in extract and extract +

DHLPPi suggest the immunomodulatory effects (Saganuwan and Ogalue, 2008). The significant decrease in serum ALP observed might be due to kidney damage because decreased level of ALP is associated with severe chronic nephritis. The increase in serum ALT and AST observed in the extract and extract + vaccine (DHLPPi) groups respectively is suggestive of liver involvement. ALT is mainly found in hepatic tissue whereas AST occurs in large concentration in cardiac as well as hepatic tissues with small amount present in other tissues (Saganuwan and Onyeyili, 2010). The finding agrees with the report of Willard et al. (1999) and Saganuwan and Ogalue (2008) indicating that ALT and AST are liver enzyme markers that could be used to indicate hepatic damage. Hyperkalemia was observed in the extract and the extract + vaccine (DHLPPi) disagrees with the findings of Saganuwan and Onyeyili indicating that Abrus precatorius extract could cause hyperkalemia. Hyponatremia and hypochloremia observed in the present study could be due to the renal damage as primary renal diseases allow the escape of the element through the urine (Saganuwan and Onyeyili, 2010). Decreased level of sodium could also be as a result of increased water gain or loss of sodium. Serum chloride regulates blood pressure, fluid and electrolyte balance, gastric fluid, and chloride shift in HCO3- transport in erythrocytes as such severe depletion of serum chloride levels (hypochloremia) can cause metabolic alkalosis characterized by mental confusion, apnea, paralysis, muscle spasm. Care may however be taken as prolong use of the plant may result to these effects (Saganuwan et al., 2014).

Conclusion

Aqueous extract of Abrus precatorius seed has immunomodulatory potentials and may be used as blood tonic and as an immune-stimulant in anemic and immune-compromised diseased conditions like chronic viral infections.

Acknowledgement. The authors appreciate the efforts of Amine Andrew A., Disa Torkuma P., and Tughgba, T who supported in handling the experimental animals and blood collection; Upev Vincent and Nande Jacob who helped out in the laboratory.

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