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    <title>DSpace Collection:</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1094</link>
    <description />
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        <rdf:li rdf:resource="http://repository.fuoye.edu.ng:80/handle/123456789/1100" />
        <rdf:li rdf:resource="http://repository.fuoye.edu.ng:80/handle/123456789/1099" />
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        <rdf:li rdf:resource="http://repository.fuoye.edu.ng:80/handle/123456789/1098" />
        <rdf:li rdf:resource="http://repository.fuoye.edu.ng:80/handle/123456789/1097" />
        <rdf:li rdf:resource="http://repository.fuoye.edu.ng:80/handle/123456789/1096" />
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    <dc:date>2026-04-16T04:26:11Z</dc:date>
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  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1100">
    <title>Acute and sub-chronic toxicity proﬁle of methanol leaf extract of Gouania longipetala in rats</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1100</link>
    <description>Title: Acute and sub-chronic toxicity proﬁle of methanol leaf extract of Gouania longipetala in rats
Authors: Asuzu, I. U; Maxwell, I. Ezeja; Aruh O., Anaga
Abstract: Ethnopharmacological relevance: Gouania longipetala leaves are commonly used in folkloric medicine in&#xD;
Africa and other parts of the world for treatment of edema, febrifuges, veneral diseases, lumbago, heart&#xD;
diseases, diabetes mellitus malaria, etc. This study therefore evaluated safety proﬁle of the methanol leaf&#xD;
extract of the plant using acute and sub-chronic studies in rat model.&#xD;
Materials and methods: Acute toxicity test of the plant lasted for 48 h with oral administration of graded&#xD;
doses (100–4000 mg/kg) of Gouania longipetala extract (GLE) in rats. The rats were observed for signs of&#xD;
toxicity and death. The sub-chronic toxicity was evaluated by administration of different doses (2.5, 5 and&#xD;
10 mg/kg) of GLE daily in feed for 90 days. On days, 30, 60 and 90, blood samples collected from the&#xD;
retro-orbital plexus of the eye of the rats were used for evaluation of serum biochemistry, hematology,&#xD;
lipid peroxidation and in vivo antioxidant activities. Histopathological evaluations of the kidney, liver,&#xD;
lungs and heart were also done.&#xD;
Results: The acute toxicity test revealed no observable signs of toxicity or morbidity. Sub-chronic study&#xD;
showed that GLE signiﬁcantly (po0.05) increased relative liver weight on day 90 at 10 mg/kg. There&#xD;
were no signiﬁcant variations in the hematological parameters of both GLE treated and untreated rats.&#xD;
The extract signiﬁcantly (po0.05) reduced total cholesterol, triglycerides, very low density lipoproteins&#xD;
and increased high density lipoproteins which was more prominent on day 90 at the dose of 10 mg/kg.&#xD;
The extract signiﬁcantly (po0.05) increased liver enzyme markers at the doses used. GLE also&#xD;
signiﬁcantly (po0.05) increased serum urea at the dose of 10 mg/kg on day 90. The extract caused&#xD;
dose-dependent and signiﬁcant (po0.05) increase in superoxide dismutase and decrease in malondiadehyde.&#xD;
Histopathological studies revealed degenerative changes in the kidney and liver.&#xD;
Conclusion: The results of the study suggest that Gouania longipetala is well tolerated in short term&#xD;
therapies, but may have long term toxic effects on the kidney and liver. vc@fuoye.edu.ng</description>
    <dc:date>2013-10-31T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1099">
    <title>The antiinflammatory activity of extracts from the root of Combretum dolichopetalum</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1099</link>
    <description>Title: The antiinflammatory activity of extracts from the root of Combretum dolichopetalum
Authors: Asuzu, I. U; Adimorah, R. I.
Abstract: The methanol and chloroform extracts of the root of Combretum dolichopetalum were obtained and&#xD;
gave yields of 6.48%&#xD;
w/w and 0.38% w/w respectively. The methanol extract significantly inhibited car­&#xD;
ageenin-induced mouse paw edema in a dose-dependent manner after an oral treatment.&#xD;
The maximum&#xD;
effect was achieved at a dose of 600 mg/kg and the result was comparable to that of indomethacin (10&#xD;
mg/kg). The antiinflammatory activity of the chloroform extract against croton-oil induced mouse ear&#xD;
edema was significant (p&#xD;
&lt; 0.001) and increased with the dose. The maximum effect (93%) was&#xD;
achieved with 1.0 mg of the extract per ear. vc@fuoye.edu.ng</description>
    <dc:date>1998-04-05T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1099">
    <title>The antiinflammatory activity of extracts from the root of Combretum dolichopetalum</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1099</link>
    <description>Title: The antiinflammatory activity of extracts from the root of Combretum dolichopetalum
Authors: Asuzu, I. U; Adimorah, R. I.
Abstract: The methanol and chloroform extracts of the root of Combretum dolichopetalum were obtained and&#xD;
gave yields of 6.48%&#xD;
w/w and 0.38% w/w respectively. The methanol extract significantly inhibited car­&#xD;
ageenin-induced mouse paw edema in a dose-dependent manner after an oral treatment.&#xD;
The maximum&#xD;
effect was achieved at a dose of 600 mg/kg and the result was comparable to that of indomethacin (10&#xD;
mg/kg). The antiinflammatory activity of the chloroform extract against croton-oil induced mouse ear&#xD;
edema was significant (p&#xD;
&lt; 0.001) and increased with the dose. The maximum effect (93%) was&#xD;
achieved with 1.0 mg of the extract per ear. vc@fuoye.edu.ng</description>
    <dc:date>1998-04-05T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1098">
    <title>The anti-snake venom activities of the methanolic extract of the bulb of Crinum jagus (Amaryllidaceae)</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1098</link>
    <description>Title: The anti-snake venom activities of the methanolic extract of the bulb of Crinum jagus (Amaryllidaceae)
Authors: Asuzu, I. U; Ode, O.J.
Abstract: The anti-snake venom activities of the methanolic extract of the bulb of Crinum jagus plant (Amaryllidaceae) were&#xD;
investigated in vitro and in vivo against the venoms of three notable snake species: Echis ocellatus, Bitis arietans and Naja&#xD;
nigricollis. The extract was prepared by cold marceration in 50% methanol at 37 1C with intermittent shaking for 48 h. An&#xD;
yield of 12.8% w/w dry extract was obtained. Oral administration of C. jagus extract (1000 mg/kg) protected 50% of mice,&#xD;
while injection of a 30 min pre-incubated mixture of the same dose of extract and venom gave 100% protection against the&#xD;
lethal effects of E. ocellatus venom (10 mg/kg, i.m.). The intraperitoneal administration of the extract at 250 mg/kg, 30 min&#xD;
before the injection of E. ocellatus venom (10 mg/kg, i.m.), signiﬁcantly (po0.05) prolonged the death time of poisoned&#xD;
mice. C. jagus extract (500 mg/kg, per os), gave 50% protection against B. arietans venom (9.5 mg/kg, i.m.) in mice while&#xD;
the pre-incubation of a mixture of the same dose of venom and extract (500 mg/kg), prior to injection (i.p.) of the mixture,&#xD;
gave only 33.3% protection. The pre-incubation of 500 mg/kg of C. jagus extract with N. nigricollis venom (6 mg/kg) prior&#xD;
to i.p. injection of the mixture protected 50% of the treated mice. There were generally no signiﬁcant differences in the&#xD;
death times of mice that were given the same dose of the extract orally 30 min before injection of the venoms and those&#xD;
administered with the pre-incubated mixtures of venom and extract. The pre-incubation of the extract and E. ocellatus&#xD;
venom (5 mg/kg) for 30 min, before the i.m. injection of the mixture, signiﬁcantly reduced inﬁltration of inﬂammatory cells&#xD;
to the site of injection 4 h post treatment. The concentrations of plasma creatine kinase in poisoned mice were signiﬁcantly&#xD;
(po0.01 or po0.05) reduced after the injection (i.p.) of C. jagus extract (1000 mg/kg) pre-incubated with E. ocellatus&#xD;
(5 mg/kg) or B. arietans (7 mg/kg) venom, respectively. The bulb extract of C. jagus blocked the haemorrhagic activity of a&#xD;
standard haemorrhagic dose (2.8 mg/ml) of E. ocellatus venom at various concentrations (1.7, 3.3 and 6.7 mg/ml). The&#xD;
methanolic bulb extract of C. jagus was therefore able to signiﬁcantly protect mice from death, myonecrosis and&#xD;
haemorrhage induced by the lethal effects of venoms of notable snake species in Nigeria. vc@fuoye.edu.ng</description>
    <dc:date>2006-06-27T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1097">
    <title>The antisnake venom activities of Parkia biglobosa (Mimosaceae) stem bark extract</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1097</link>
    <description>Title: The antisnake venom activities of Parkia biglobosa (Mimosaceae) stem bark extract
Authors: Asuzu, I. U; Harvey, A.L.
Abstract: Snake bites in rural Nigeria are commonly treated with plant extracts. We have studied the ability of one such traditionally&#xD;
used plant (Parkia biglobosa; [Jacq.] Benth., Mimosaceae) to reduce the effects of two snake venoms (Naja nigricollis, and&#xD;
Echis ocellatus) in several experimental models. A water-methanol extract of P. biglobosa stem bark signiﬁcantly ðp , 0:001Þ&#xD;
protected the chick biventer cervicis (cbc) muscle preparation from N. nigricollis venom-induced inhibition of neurally evoked&#xD;
twitches when it was added to the bath 3–5 min before or after the venom. The extract also reduced the loss of responses to&#xD;
acetylcholine (Ach), carbachol and KCl, which are normally blocked by N. nigricollis venom, and signiﬁcantly reduced the&#xD;
contractures of the preparation induced by venom. P. biglobosa extract (75, 150 and 300 mg/ml) signiﬁcantly ðp , 0:05Þ&#xD;
protected C&#xD;
2&#xD;
C&#xD;
murine muscle cells in culture against the cytotoxic effects of N. nigricollis and E. ocellatus venoms. The&#xD;
extract protected egg embryos exposed to lethal concentrations of E. ocellatus venom for more than 12 h and completely&#xD;
blocked the haemorrhagic activity of the venom at concentrations of 5 and 10 mg/1.5 ml. P. biglobosa extract (400 mg/kg) did&#xD;
not protect mice injected i.p. with 5 and 2.5 mg/kg of E. ocellatus and N. nigricollis venoms, respectively. It, however, protected&#xD;
40% of the mice from death caused by E. ocellatus venom after the extract and venom were pre-incubated for 30 min before&#xD;
injecting the mixture. vc@fuoye.edu.ng</description>
    <dc:date>2003-10-06T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1096">
    <title>The anthelmintic activity of D-3-O-methylchiroinositol isolated from Piliostigma thonningii stem bark</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1096</link>
    <description>Title: The anthelmintic activity of D-3-O-methylchiroinositol isolated from Piliostigma thonningii stem bark
Authors: Asuzu, I. U; Gray, A.I.; Waterman, P.G.
Abstract: Piliostigma thonningii Schum. Milne-Redhead Caesalpiniaceae , dried&#xD;
stem bark collected from Nsukka in September 1990 and identified by Mr A.&#xD;
Ozioko of the Department of Botany, University of Nigeria, Nsukka, where&#xD;
voucher specimen is deposited in the herbarium. vc@fuoye.edu.ng</description>
    <dc:date>1998-05-08T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1095">
    <title>The effects of hyperosmolar agents lithium chloride and sucrose on the brain concentration of diminazene aceturate in rats</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1095</link>
    <description>Title: The effects of hyperosmolar agents lithium chloride and sucrose on the brain concentration of diminazene aceturate in rats
Authors: Asuzu, I. U; Odika, I.E; Anika, S.M.
Abstract: The concentrations of diminazene aceturate in the brain of Trypanosoma brucei brucei infected and&#xD;
uninfected rats treated with diminazene aceturate (3.1 mg/kg, im) and either LiC1 (2.5, 5.0 and 10 ~tg/kg)&#xD;
or sucrose (0.25, 0.5 and 1.0 g/kg) were determined. When diminazene aceturate was administered at a&#xD;
standard dose of 3.1 mg/kg (ira), the addition of LiCI (10 ~tg/kg, ira) increased significantly (P&lt; 0.05) the &#xD;
concentration of the drug in the brains of both trypanosome infected and normal infected rats. The&#xD;
addition of sucrose (1.0 g/kg, im) instead of LiCI failed to give any significant increase in diminazene&#xD;
aceturate levels in the brain. The diminazene aceturate levels were significantly (P&lt;0.05) higher in the &#xD;
organs (brain, kidney, liver and spleen) of trypanosome infected compared to uninfected rats. The concen-&#xD;
tration of diminazene aceturate in the organs increased significantly (P&lt;0.05) with increasing concen-&#xD;
trations of LiC1. vc@fuoye.edu.ng</description>
    <dc:date>1994-04-05T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1095">
    <title>The effects of hyperosmolar agents lithium chloride and sucrose on the brain concentration of diminazene aceturate in rats</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1095</link>
    <description>Title: The effects of hyperosmolar agents lithium chloride and sucrose on the brain concentration of diminazene aceturate in rats
Authors: Asuzu, I. U; Odika, I.E; Anika, S.M.
Abstract: The concentrations of diminazene aceturate in the brain of Trypanosoma brucei brucei infected and&#xD;
uninfected rats treated with diminazene aceturate (3.1 mg/kg, im) and either LiC1 (2.5, 5.0 and 10 ~tg/kg)&#xD;
or sucrose (0.25, 0.5 and 1.0 g/kg) were determined. When diminazene aceturate was administered at a&#xD;
standard dose of 3.1 mg/kg (ira), the addition of LiCI (10 ~tg/kg, ira) increased significantly (P&lt; 0.05) the &#xD;
concentration of the drug in the brains of both trypanosome infected and normal infected rats. The&#xD;
addition of sucrose (1.0 g/kg, im) instead of LiCI failed to give any significant increase in diminazene&#xD;
aceturate levels in the brain. The diminazene aceturate levels were significantly (P&lt;0.05) higher in the &#xD;
organs (brain, kidney, liver and spleen) of trypanosome infected compared to uninfected rats. The concen-&#xD;
tration of diminazene aceturate in the organs increased significantly (P&lt;0.05) with increasing concen-&#xD;
trations of LiC1. vc@fuoye.edu.ng</description>
    <dc:date>1994-04-05T00:00:00Z</dc:date>
  </item>
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