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ON TESTIS AND EPlDlDYMlS OF RATS - Pondicherry University ...

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cytoplasmic droplets shed from sperm dwing epididymal transit (Henno er 01.. 1988).<br />

The journey from the testis to the cauda epididymis has been shown to take<br />

approximately 4 days in rats (Klinefelter and Hess, 1998).<br />

Estrogen has also been shown to play an important role in fluid reabsorption in<br />

efferent ductulcs and epididymis of rats (Hess et a[., 1997; Hess et al., 2000). Effect<br />

of estrogen on the epididymis can be viewed either as indirect or direct. since<br />

estradiol is a potent suppressor of LH secretion. Administration of estradiol results in<br />

a decrease in gonadotrophins and consequently in a shutdown of Leydig cell function,<br />

and hence androgen production. The presence of aromatase activity has been reported<br />

in spermatozoa entering the epididymis (Janulis et al., 1998) and of estrogen receptors<br />

in epididymal principal cells (Hess et al., 1997). Estrogen has been shown to cause<br />

reduction in epididymal sperm number and motility in adult male rats (Kaneto er al.,<br />

1999).<br />

1.2 Target organ response to testosterone<br />

Accessory sex organs in male have been reported to be androgen dependent<br />

and thus reflect the availability of androgens (Hunt el al., 1978). Weights of the<br />

accessory sex organs in castrated male rats have been widely used as a bioassay for<br />

androgenic and antiandrogenic compounds (Neumann and Steinbeck, 1974).<br />

Weights. sizes, cytological structures and mitotic activity of the seminal vesicles of<br />

mouse were established as indicators of bioassay for androgenic hormones (Deanesly<br />

and Parkes, 1933). Measurement of weights of the accessory sex organs in intact rats<br />

has been shown to reflect the estimation of cumulative effect of biologically active<br />

testosterone over a period (Mathw and Chattopadhyny. 1982).<br />

The sensitivity of the accessory sex organs varied from organ lo orgun 21s<br />

shown by the requirement of androgen for seminal vesicles being 3 times more than<br />

that of prostate (Moore and Gallagher. 1930; Burkhart. 1942). The maintenance of<br />

structural and functional integrity of prostate gland has ken reported to be dependent<br />

upon the amount of circulating androgen pr$nccd by the testis (Butler and Schode,

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