Histomorphometric studies of the effects of Telfairia occidentalis on alcohol-induced gonado-toxicity in male rats.

BACKGROUND: Available evidence suggests that 50% of couples with infertility are male related. Over 40% of these males consume alcohol which has been reported to be a reproductive toxicant causing depletions in the epithelium of seminiferous tubules hence reducing sperm counts and sperm morphology. OBJECTIVE: To determine the effects of aqueous leaf extract of Telfairia occidentalis on alcohol-induced cyto-architectural changes in the testis. METHODS: Aqueous leaf extract of Telfairia occidentalis (T. occidentalis) was administered by gastric gavage at a dose of 250 mg/kg and 500 mg/kg body weight daily, while 2 g/kg body weight of ethanol at 30% v/v was administered daily to mature male Sprague-Dawley rats. The experiment was in 2 phases. Phase 1 had groups A1-F1 and lasted for 4 weeks while phase 2 had groups A2-F2 and lasted 8 weeks. Parameters tested include: testicular histology, relative volume density, sperm parameters, malondialdehyde (MDA), superoxide dismutase (SOD) and reduced glutathione. RESULTS: In both phases, there were depletions in the seminiferous epithelium, decreased sperm quality and increased MDA and SOD in animals that received alcohol only compared to control. Likewise, a significant increase of seminiferous epithelium of animals that received respective doses of 250 mg/kg and 500 mg/kg of T. occidentalis only compared to control. Animals that received T. occidentalis and alcohol simultaneously had a significant increase in seminiferous epithelium and sperm quality with decreased MDA level. CONCLUSION: T. occidentalis attenuated the deleterious effects of alcohol to the cyto-architecture of the testis, protected the seminiferous epithelium, reduced oxidative stress and promoted spermatogenesis.

Factors influencing extract of Hibiscus sabdariffa staining of rat testes.

Some plant extracts can be used in biology and medicine to reveal or identify cellular components and tissues. We investigated the effects of time and concentration on staining of histological sections of rat testes by an acidified extract of Hibiscus sabdariffa. An ethanolic extract of H. sabdariffa was diluted using 1% acetic acid in 70% ethanol to stain histological sections of testes at concentrations of 0.2, 0.1 and 0.05 g/ml for 5, 10, 15, 30, 45 and 60 min. The sections of testes were stained deep red. The staining efficiency of H. sabdariffa was greater at a high concentration and required less time to achieve optimal staining. H. sabdariffa is a strongly basic dye that can be used for various diagnostic purposes. Staining time and concentration must be considered to achieve optimal results.

Phenytoin-induced Toxicity in the Postnatal Developing Cerebellum of Wistar Rats, Effect of Calotropis procera on Histomorphometric Parameters / Toxicidad Inducida por Fenitoína en el Desarrollo Postnatal del Cerebelo de Ratas Wistar, Efecto de Calotropis procera sobre los Parámetros Histomorfométricos

The role of methanolic leaf extracts of Calotropis procera in phenytoin-induced toxicity on histomorphometric variables in the postnatal developing cerebellum of Wistar rat was studied. Pregnant rats were treated orally with 50 mg/kg phenytoin in pre and post natal life and 300 mg/kg methanolic leaf extract of Calotropis procera 1 hour prior to phenytoin administration. 200 mg/kg vitamin C (standard antioxidant) was also administered orally 1 hour prior to phenytoin treatment. The control animals received water. Standard diet of rat pellets and water were provided ad libitum. At the end of the experiment, the offspring of days 1, 7, 14, 21, 28 and 50 post partum, five per group were sacrificed by cervical dislocation. The cerebellum of all groups were dissected out and processed for histomorphometric studies. The results showed in the developing cerebellum of phenytoin treated animals, a delayed cell maturation in the external granular layer, reduction of the molecular layer, astrocytic gliosis and loss of Purkinje cells on day 50 postpartum. Administration of extracts of Calotropis procera and vitamin C though reversed these changes when compared with the phenytoin treated group, but not significantly when compared with the control. In conclusion, supplementation with methanolic extracts of Calotropis procera reduced the rate at which phenytoin induced toxicity in the postnatal developing cerebellum of Wistar rat.

Fue estudiado el rol de los extractos metanólicos de las hojas de Calotropis procera en la toxicidad inducida por fenitoína sobre las variables histomorfométricas en el desarrollo postnatal del cerebelo de ratas Wistar. Ratas preñadas fueron tratadas por vía oral con 50 mg/kg de fenitoína durante la vida pre y post natal. Además, fue administrado, por vía oral, una hora antes del tratamiento con fenitoína 300 mg/kg de extracto metanólico de las hojas de Calotropis procera y 200 mg/kg de vitamina C (antioxidante estándar). Los animales control recibieron agua. Una dieta estándar de pellets para rata y agua se proporcionaron ad libitum. Al final del experimento, 5 crías por grupo de 1, 7, 14, 21, 28 y 50 días post parto, fueron sacrificadas por dislocación cervical. El cerebelo de todos los animales de los diferentes grupos fueron disecados y procesados para el estudio histomorfométrico. Los resultados mostraron en el desarrollo del cerebelo de los animales tratados con fenitoína un retraso en la maduración de células en la capa granular externa, reducción de la capa molecular, gliosis astrocitaria y pérdida de las células de Purkinje en el día 50 post parto. La administración de extractos de Calotropis procera y vitamina C, aunque invirtieron estos cambios, en comparación con los grupos tratados con fenitoína, no fueron significativos en comparación con el control. En conclusión, la suplementación con extractos metanólicos de Calotropis procera redujo la velocidad a la que la fenitoína induce toxicidad en el desarrollo postnatal del cerebelo de ratas Wistar.

The antifertility effect of amodiaquine hydrochloride.

BACKGROUND: A number of antimalarial compounds and herbs have been reported to possess antifertility actions. Amodiaquine (AQ) belongs to the same class of drugs as chloroquine. Chloroquine has been reported to disrupt the oestrus cycle, block ovulation and consequently reduce fertility. OBJECTIVE: This study was carried out to investigate the effect of the administration of amodiaquine hydrochloride (AQ.HCl) on fertility in the adult cyclic Sprague-Dawley rats. METHODS: Thirty cycling female albino rats of Sprague-Dawley strain weighing 120 g were used in this experiment. They were divided into six experimental groups. Groups 1A, 1B and 1C- received peroral (p.o.) 6 mg/kg bw of AQ.HCl, 12 mg/kg bw of AQ.HCl and distilled water for 28 days respectively to determine the effect of AQ.HCl on the oestrous cycle. Groups 2A, 2B and 2C- received a single dose p.o. of 6 mg/kg bw of AQ.HCl, 12 mg/kg bw of AQ.HCl and distilled water at 9 a.m. on proestrus respectively to determine the effect of AQ.HCl on ovulation and the serum concentrations of follicle stimulating hormone (FSH), luteinizing hormone (LH) and prolatin (PRL). RESULTS: AQ.HCl disrupted the oestrous cycle by producing a significant (p < 0.05) increase in the diestrus phase and a reduction in the other phases when compared with the control. A significant reduction (p < 0.05) in the number of ova shed on estrus was observed however, there was no significant difference in the serum concentrations of FSH, LH and PRL when compared with the control. CONCLUSION: Oral administration of AQ.HCl distrupts the oestrous cycle and ovulation by increasing the frequency of the diestrus phase and reducing the number of ova released at ovulation respectively. These events may negatively affect fertility in females of reproductive age.

Effect of aqueous extract of the bark of Carica papaya on testicular histology in Sprague-Dawley rats.

BACKGROUND: Males generally have few options for controlling their fertility and these options are far from being satisfactory. There is a great need for research to develop more contraceptive modalities for males. OBJECTIVE: The overall aim of this research was to determine the histological responses of the testes of Sprague-Dawley rats to aqueous extract of bark of Carica papaya using a single daily dose of 100 mg/kg and also to investigate if these responses are reversible or not. MATERIALS AND METHODS: Sixty mature (6-8 weeks old) male Sprague-Dawley rats, divided into 2 equal groups, were used for this experiment. Group 1 rats were fed with 100 mg/kg/day of the extract for 4 and 8 weeks, while group 2 rats served as the control subjects. Each cauda epididymis of the rats was exteriorized, incised and sperm motility and count conducted on expressed fluid. The testes were harvested and processed for histological examination under light microscope. Phytochemical analysis was done to ascertain the main constituents in the extract, while the LD50 was conducted to guide in the dose of administration of the extract. A subgroup of the animals was allowed a recovery period of 8 weeks before sacrifice. RESULTS: The results showed that 500 mg/kg (LD50) of the extract of bark of Carica papaya produced signs of toxicity with mortality of 50% of the rats. The extract at a dose of 100 mg/kg caused histological changes ranging from seminiferous tubular distortion to outright destruction/ degeneration of the seminiferous tubules. In addition, the testicular interstitia of extract-treated rats showed disorganization and hypocellularity. The extract also caused a significant (p < 0.05) reduction in both sperm count and motility. There was no significant reversal of these antispermatogenic effects following a recovery period of 8 weeks. CONCLUSION: Aqueous extract of the bark of Carica papaya has deleterious effects on both the seminiferous tubules and testicular interstitium and deserves to be further investigated as a potential male contraceptive agent.

The prevalence of agenesis of palmaris longus muscle amongst students in two Lagos-based medical schools / Prevalencia de agenesia del músculo palmar largo entre estudiantes en dos escuelas médicas en Lagos

Palmaris longus (PL) muscle, although of little functional use to the human upper limb, assumes great importance when used as a donor tendon for transfer or transplant. The surgeon's awareness of the incidence in a population is therefore desirable. In the present study, 500 Medical students (242 males and 258 females) of ages 16 to 40 years from both College of Medicine of the University of Lagos, Idi-Araba and Lagos State University College of Medicine, Ikeja were examined for the presence or absence of the PL tendon, using the conventional (Schaffer's) test. The prevalence and pattern of PL agenesis was further analyzed statistically for differences in the prevalence or pattern of PL agenesis with regard to body side or sex. The prevalence of PL agenesis was found to be 12.6 percent (8 percent Unilateral and 4.6 percent Bilateral). Out of those with unilateral agenesis, 20 (4 percent) had left-sided agenesis and 20 (4 percent) had right-sided agenesis. Although female subjects had a prevalence of agenesis of PL tendon (Unilateral and Bilateral combined) of 36 out of 258, (13.95 percent) while in male subjects this prevalence was 23 out of 242 (9.5 percent). The prevalence of PL muscle agenesis in this study was found to be much higher than the reported average for blacks (2-3 percent).

El músculo palmar largo (PL), aunque de poco uso funcional en el miembro superior humano, asume gran importancia cuando se utiliza como un tendón donante para la transferencia o trasplante. El cirujano ha tomado conciencia que la incidencia en una población es por tanto deseable. En el presente estudio, 500 estudiantes de medicina (242 hombres y 258 mujeres) de 16 a 40 años, de la Facultad de Medicina de la Universidad de Lagos (Idi-Araba) y la Facultad de Medicina de la Universidad Estatal de Lagos (Ikeja) fueron examinados para evaluar la presencia o ausencia del tendón del PL, utilizando la prueba convencional (Schaffer's). La prevalencia y el patrón de agenesia del PL fueron determinados para analizar diferencias estadísticas en la prevalencia o patrón de agenesia del PL con respecto al lado del cuerpo o sexo. Se encontró una prevalencia de agenesia del PL de 12,6 por ciento (8 por ciento y 4,6 por ciento unilateral y bilateralmente). De los sujetos con agenesia unilateral, 20 (4 por ciento) eran en el lado izquierdo y 20 (4 por ciento) en el lado derecho. Las mujeres tuvieron una prevalencia de agenesia del tendón del PL (unilaterales y bilaterales combinadas) en 36 de 258 (13,95 por ciento), mientras que en los hombres esta prevalencia fue en 23 de 242 (9,5 por ciento). La prevalencia de agenesia del músculo PL en este estudio se encontró mucho más alto que el promedio reportado para los negros (2-3 por ciento).

Effect of methanolic seed extract of Momordica charantia on body weight and serum cholesterol level of male Sprague-Dawley rats.

BACKGROUND: A steady weight increase disproportionate to height is by far the most prevalent type of body weight imbalance (overweight and obesity) in apparently healthy individuals of growing age. Many subsisting weight-reduction regimes or formulations are ineffective. Therefore, an effective and affordable weight-reduction product will add to the options available for the management of weight-related conditions. OBJECTIVE: This study aimed to investigate the effects of graded oral doses of methanolic seed extract of Momordica charantia (MC) on the body weights and cholesterol levels of male rats. MATERIALS AND METHODS: Twenty adult male Sprague-Dawley rats, weighing 176 +/- 70 g, were used for this study. The animals, divided randomly into 4 groups (A-D) received daily graded oral doses of 15, 25 and 50 mg/100 g body weight of methanolic seed extract of MC, respectively, while Group D rats had distilled water for 56 days. The weights of the animals in each group were recorded weekly throughout the duration of the experiment. Serum cholesterol levels were assayed from blood obtained from a left ventricular puncture. RESULTS: Treatment of rats with MC extract resulted in a dose-dependent, statistically significant (p < 0.05; p < 0.01) reduction in the body weight compared to control. The mean serum cholesterol levels in response to graded doses of MC in the different groups A to C also showed a statistically significant decrease (p < 0.05) from the baseline control value of 4.4 +/- 1.0 mMol/L to 3.4 +/- 0.7, 2.5 +/- 0.4 and 2.0 +/- 1.3 mMol/L, respectively. CONCLUSIONS: Present study demonstrated that MC caused dose-dependent reductions in body weight and serum cholesterol concentration in male Sprague-Dawley rats. MC may, therefore, be useful in controlling body weight increase in individuals of growing age as well as be a potential agent in the management of overweight and obesity.

Antifertility potential of Neem flower extract on adult female Sprague-Dawley rats.

BACKGROUND: The search for a relatively cheap, widely available, widely accepted and effective contraceptive of plant origin; that is equally non-invasive in administration, non-hormonal in action, non-toxic and that is relatively long-acting, generated our interest in this study (in order to meet the increasing need for population control). The aim of this study was to determine the effects of alcoholic extract of Neem flowers on the estrous cycle, ovulation, fertility and foetal morphology of cyclic adult Sprague-Dawley rats. MATERIALS AND METHODS: Adult female Sprague-Dawley rats, weighing between 140-180 g were used. There were 3 main experimental groups. Group 1 rats received 1 g/kg of alcoholic extract of Neem flower by gavage for 3 weeks and the effect on estrous cycle studied. Group 2 rats were administered 1 g/kg of Neem flower alcoholic extract at 9 a.m. and at 6 p.m. on proestrus and the effect on the number of ova shed on the morning of estrus observed. Rats in Group 3 were treated with 1 g/kg of alcoholic extract of Neem flower on days 1 to 5 postcoitum, and observation was made for anti-implantation / abortifacient effects and possible teratogenic effects on the foetuses. All the groups were control-matched. RESULTS: The estrous cycle of 80% of the rats was altered with a marked prolongation of the diestrus phase. Neem flower caused a statistically significant (p < 0.05) reduction in the number of ova shed in the morning of estrus in rats fed with the extract at 9 a.m. on proestrus. Neither anti-implantation / abortifacient nor teratogenic effect was observed in the rats treated with Neem flower. CONCLUSION: Administration of alcoholic extract of Neem flower disrupted the estrous cycle in Sprague-Dawley rats and caused a partial block in ovulation and thus has the potential of being developed into a female contraceptive.

The effect of quinine and ascorbic acid on rat testes.

BACKGROUND: We have previously demonstrated that quinine is a testicular toxicant in Sprague-Dawley rat. OBJECTIVE: To describe the changes in the testicular levels of testosterone and lipid peroxidation secondary to quinine and ascorbic acid administration in rats. METHODS: Twenty male Sprague-Dawley rats per group were assigned to one of three treatment groups: 0 mg quinine and 0 mg ascorbic acid/kg body weight (control); 10 mg quinine/ kg BW; and 10 mg quinine plus 0.1 mg ascorbic acid/kg BW. Rats were intramuscularly administered their respective doses of quinine five days in a week and ascorbic acid three days in a week for eight weeks. All the animals were sacrificed at the end by decapitation. Seminal analysis was performed on tubular fluid from caudal epididymides. Evaluations were made for testicular levels of testosterone and lipid peroxidation through malondialdehyde (MDA). Testicular specimens were also processed for histology under light microscopy. RESULTS: Quinine significantly (p < 0.01) increased free radicals (from elevation of MDA) and decreased testosterone in the testis compared with those of the control group and those treated with a combination of quinine and ascorbic acid. The semen of rats treated with only quinine demonstrated a significantly (p < 0.001) lower sperm concentration and motility compared to the controls and those treated with quinine plus ascorbic acid. Microscopic examination of cross-sections of seminiferous tubules also showed that ascorbic acid partially protected against quinine -induced testicular effects. CONCLUSION: Ascorbic acid has beneficial effect and protects against quinine-induced testicular reduction of testosterone.

Quinine lowers serum and testicular testosterone in adult Sprague-Dawley rats.

We have earlier demonstrated that quinine (QU) is a testicular toxicant. This present study was aimed at evaluating the effects of QU on both the serum and testicular levels of testosterone (TT) in an attempt to elucidate one of the potential mechanisms of QU-induced testicular toxicity. Thirty adult male Sprague-Dawley rats weighing 180-200g were used and were randomly divided into 3 groups of 10 rats each. Rats in group 1 had distilled water. Rats in group 2 had QU only at the dose of 10 mg/kg body weight per day (5 days in a week) for 8 weeks. Rats in group 3 rats had 10 mg/kg of QU (5 days in week) and 0.05 mg/kg of TT (3 days in a week) for 8 weeks. All the animals were sacrificed at the end of 8 weeks by decapitation. Seminal analysis was done on the tubular fluid aspirated from the caudal epididymides. The two testes were excised, weighed, and volume estimated. One testis of each rat (0.25 g of tissue) was homogenized with Potassium Chloride and TT level determined in the supernatant of the homogenate, while the other testis was processed for histology. Morphometry was carried out by assessing the diameter, cross-sectional area, number of profiles per unit area, length density and numerical density of the seminiferous tubules, and the relative and absolute volume of testicular components. The serum levels of TT in all the animals were also determined at the time of sacrifice. Both the serum and testicular levels of TT in rats administered QU only were significantly (P < 0.001) lower than those of the control and QU plus TT-treated rats. We conclude that QU induces spermatogenic epithelial toxicity by possibly interfering with the steroidogenic function of the Leydig cell.

Morphometric and stereological assessment of the effects of long-term administration of quinine on the morphology of rat testis.

BACKGROUND AND OBJECTIVES: Quinine (QU) has been used worldwide in the suppression and treatment of malaria for more than 350 years. The aim of this study was to determine the long-term morphological response of the testis to long-term administration of QU using stereological parameters. MATERIALS AND METHODS: 64 adult male Sprague-Dawley rats weighing 180-200g were used. The animals were randomly divided into 8 groups of 8 rats each. Every experimental animal had intramuscular QU at a dose of 10mg/kg body weight per day (5 times in a week, with the exception of group 1 animals). Group 1 rats had QU for 1 week (7 days consecutively) and were sacrificed on the last day of injection. Groups 2 and 3 rats had QU for 4 and 6 weeks and were sacrificed at the end of the 4th and 6th week respectively. Group 4, 5, 6 and 7 rats had QU for 8 weeks and were sacrificed at the end of week 8, 12, 16 and 20 respectively. Group 8 animals constituted the controls and had equal volume of distilled water intramuscularly for 8 weeks. All sacrifices were by decapitation. The testes were carefully dissected out, their volumes measured, weighed and histological sections prepared. Morphometric assessment was carried out using the diameter, cross-sectional area, number of profiles per unit area, numerical density and volume density of the seminiferous tubules and the relative and absolute volume of the seminiferous epithelium, stroma and lumen of tubules. RESULTS: The results showed that there was a general destruction of cells of the seminiferous tubules and the testicular interstitium that persisted even after the discontinuation of QU and to the end of our experiment that lasted 20 weeks. CONCLUSION: We conclude that QU has deleterious effect on the seminiferous tubules of Sprague-Dawley rats, though the mechanism of damage is unclear.

Attenuation of quinine-induced testicular toxicity by ascorbic acid in rat: a stereological approach.

Quinine (QU), an alkaloid derived from the cinchona bark is presently the mainstay of treatment for severe malaria and nocturnal leg cramps. We have recently demonstrated that QU is toxic to testicular gonocytes and interstitial endocrinocytes. This present study sought to determine whether co-administration of ascorbic acid (AA) with QU will modify the deleterious effects of QU on the testes of Sprague-Dawley rats. 50 male Sprague-Dawley rats weighing 160-180g were used for the experiments. The animals were randomly divided into 5 groups of 10 rats each and were variously administered QU for 7 days, QU for 8 weeks, QU plus AA for 7 days, QU plus AA for 8 weeks and distilled water. They were all sacrificed on the 56th day. Histological slides of the testes were prepared and morphometric parameters that included diameter and cross-sectional area of the seminiferous tubules, number of profiles of seminiferous tubules per unit area of testis and numerical density of the seminiferous tubules, volume density and absolute volume of testicular components were determined using a systematic random scheme. Our results showed that the cytoarchitecture of seminiferous tubules of rats treated with QU only was grossly distorted, while that of rats that had both QU and AA was not significantly different from that of the controls. The testicular volume; diameter and cross-sectional area of seminiferous tubules; and the relative and absolute volume of seminiferous epithelium of QU-treated rats were significantly (P < 0.05) reduced, while those of QU plus AA-treated Ones were not significantly different from those of the controls. In contrast, the numerical density of the tubules were significantly (P < 0.05) increased in rats administered QU only, while it was not significantly different in the QU plus AA-treated and control rats. We conclude that co-administration of AA with QU could play an important role in the modulation of QU-induced testicular damage.