“…Anterior hypothalamic lesions (Biggard and Alexander, 1939;Dey, 1943;Soulairac, 1963), lesions of the medio-basal hypothalamus including the stalk (Hetherington and Ranson, 1940;Busta-mente and co-workers, 1942;Spatz et al, 1948;Gaup, 1950;Barrnett and Greep, 1951;Spatz, 1951;Fulop, 1952;Mess, 1952;Bogdanove and Halmi, 1953;Benoit and Assenmacher, 1955;Gaup and Spatz, 1955;Bogdanove, 1957;Davidson and Sawyer, 1961;Flerko, 1962;Halasz et al, 1963;Corbin, 1963) and lesions of the posterior hypothalamus including injury of the mamillary body (Soulairac andSoulairac, 1956, 1959;Marescotti et al, 1961;Corbin, 1963) result in testicular atrophy. The arcuate (Gaup and Spatz, 1955;Ganong et al, 1955;Ganong and Hume, 1956;Bogdanove, 1957), supraoptic (Biggart and Alexander, 1939;Dey, 1943) and mamillary nuclei (Dempsey and Rioch, 1939 ;Bard, 1940;Marescotti et al, 1961;Soulairac, 1963) were included in some of these hypothalamic lesions, and this resulted in the loss or degeneration of the nerve cells and consequent glial proliferation after the lesion. Several authors, however, did not detect testicular atrophy after lesions of the mamillary body or suprachiasmatic region (Bustamente et al, 1942;Szentagothai et al, 1962;…”