AIMTo observe the effect of the aqueous extract of hypocotyls of the plant Lepidium meyenii (Maca) on spermatogenic damage induced by the organophosphate insecticide malathion in mice.

METHODSMice were treated with 80 mg/kg of malathion in the presence or absence of an aqueous extract of Maca, which was orally administered 7, 14 or 21 days after injection of the malathion. Stages of the seminiferous epithelium were assessed by transillumination on days 0, 7, 14 and 21.

RESULTSThe administration of Maca increased significantly the length of stage VIII on days 7, 14 and 21 of treatment compared with the controls. An increase in the length of stage IX occurred on day 14 of treatment. Malathion affected spermatogenesis by reducing the lengths of stage IX on day 7, stages VII and IX-XI on day 14 and a recovery of stages IX-XII on day 21. The magnitude of alteration in the length of stage IX produced by malathion was significantly reduced by Maca on days 7 and 14. The length of stage VIII was increased when Maca was administered to mice treated with malathion. Assessment of the relative length of stages of the seminiferous epithelium showed that Maca treatment resulted in rapid recovery of the effect of malathion.

CONCLUSIONMaca enhances spermatogenesis following spermatogenic damage caused by the organophosphorous pesticide.

Animals ; Drug Administration Schedule ; Hypocotyl ; Lepidium ; Malathion ; adverse effects ; Male ; Mice ; Phytotherapy ; Plant Extracts ; therapeutic use ; Spermatogenesis ; drug effects ; Time Factors ; Treatment Outcome

AIMTo evaluate the effect of a protein synthesis inhibitor cycloheximide on arresting activity in spermatogenesis and sperm count in male rats.

METHODSThe study used seminiferous tubule (ST) segments from adult rats cultured in vitro with or without cycloheximide to condition culture media, which have been concentrated, size fractioned (30-50 kDa) and administered 7 days to adult rats by intraperitoneal injections. The effects on testicular and epididymal weights, spermatogenesis and epididymal sperm count were determined.

RESULTSThe fraction (30-50 kDa), named arresting, obtained from the culture without cycloheximide decreased testicular and epididymal weights (P<0.01) and reduced the epididymal sperm count significantly. Study of the spermatogenic cycle by transillumination showed spermatogenic arrest at stage VII in rats treated with arresting compared to that observed in controls. The length of stage VII in the group receiving the seminiferous tubules culture media with cycloheximide (30-50 KDa CHX-STCM fraction) was similar to control.

CONCLUSIONThe difference in the effect may be the result of the presence or absence of arresting, a protein secreted by the tubules.

Animals ; Arrestin ; biosynthesis ; Culture Media, Conditioned ; Cycloheximide ; pharmacology ; Epididymis ; cytology ; drug effects ; growth & development ; Male ; Protein Synthesis Inhibitors ; pharmacology ; Rats ; Seminiferous Epithelium ; cytology ; drug effects ; physiology ; Seminiferous Tubules ; metabolism ; Sperm Count ; Testis ; drug effects ; growth & development

AIMTo evaluate the effect of the alcoholic extract of Lepidium meyenii (Maca) on the spermatogenesis in male rats.

METHODSIn Holtzman rats, Maca alcoholic extract (5 %) was given by oral route at doses of 48 mg/day or 96 mg/day for 7 days, 14 days and 21 days. Testicular function was assessed by measurements of lengths of different stages of seminiferous epithelia and by epididymal sperm count.

RESULTSEthanolic extract of Maca increased the length of stages IX-XI of seminiferous epithelium at treatment day 7, day 14 and day 21. Progression of spermatogenesis was evident only after day 21 when lengths of stages XII-XIV of seminiferous epithelium were increased; at day 7 and day 14, no important change in spermatogenesis was observed. Epididymal sperm count was increased with 48 mg/day at all times. With 96 mg/day an increase in sperm count was observed at day 7, but it was reduced at day 14 and day 21 of treatment. Serum testosterone levels were not affected.

CONCLUSIONThe alcoholic extract of Maca activates onset ant progression of spermatogenesis at 48 mg/day or 96 mg/day in rats.

Animals ; Epididymis ; cytology ; Ethanol ; Lepidium ; chemistry ; Male ; Plant Extracts ; administration & dosage ; pharmacology ; Rats ; Seminiferous Epithelium ; anatomy & histology ; drug effects ; Sperm Count ; Spermatogenesis ; drug effects ; Testis ; drug effects ; physiology ; Testosterone ; blood

AIMTo determine the effect of two different extracts of red maca in male rats.

METHODSProstatic hyperplasia was induced in male rats with testosterone enanthate (TE). The study comprised six groups: one control group (group 1), one group treated with TE (group 2), two groups treated with TE and aqueous extract of red maca (groups 3 and 4), one group treated with hydroalcoholic extract of red maca (group 5) and one group treated with finasteride (0.1 mg, group 6). Differences in the aqueous extract dependent on the length of time of boiling, whether for 2 or 3 hours, for groups 3 and 4 was assessed. Extracts of red maca contained 0.1 mg of benzylglucosinolate. Thereafter, a dose-response effect of different doses of benzylglucosinolates (0.02-0.08 mg) in red maca extracts was assessed.

RESULTSProstate weight was similar in rats treated with freeze-dried aqueous extract of red maca prepared after 2 and 3 hours of boiling. Freeze-dried aqueous extract of red maca, hydroalcoholic extract of red maca and finasteride reduced prostate weight in rats with prostatic hyperplasia. No difference was observed between the data obtained from aqueous extract or hydroalcoholic extract of red maca. A dose dependent reduction of prostate weight was observed with the increase of the dose of benzylglucosinolates in red maca extracts.

CONCLUSIONThe present study showed that hydroalcoholic or aqueous extract of red maca containing 0.1 mg of benzylglucosinolate can reduce prostate size in male rats in which prostatic hyperplasia had been induced by TE.

Alcohols ; Animals ; Finasteride ; therapeutic use ; Lepidium ; Male ; Organ Size ; drug effects ; Plant Extracts ; therapeutic use ; Prostate ; drug effects ; pathology ; Prostatic Hyperplasia ; chemically induced ; drug therapy ; pathology ; Rats ; Testosterone ; analogs & derivatives ; Thiocyanates ; analysis ; pharmacology ; Thioglucosides ; analysis ; pharmacology ; Water