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To determine whether increases in sagittal sinus pressure were related to disruption in venules or sufficient to account for disruption in venules. Also, because arteriolar pressure, as well as venous pressure, increases during acute hypertension, one could not exclude a contribution of increases in arteriolar pressure to disruption of the BBB during acute hypertension. Two new approaches in the present study allow us to extend the findings of previous studies. First, we measured pressure and diameter at the site of disruption, i.e., small venules. Second, we used superior venae cavae occlusion to determine whether increases in cerebral venous pressure, during acute hypertension, were sufficient in magnitude to account for disruption of the BBB. We found that disruption during acute hypertension was associated with a marked elevation of pial venular pressure and diameter. Experiments in which we occluded the superior venae cavae allowed us to dissociate changes in arteriolar pressure and venular pressure. During occlusion of the superior venae cavae, we observed increases in pial venular pressure that were similar to the increases during acute hypertension, but pial arteriolar pressure did not increase. More importantly, we observed a similar increase in clearance of FITC-dextran during superior venae cavae occlusion and acute hypertension, even though arteriolar pressure decreased during superior venae cavae occlusion. These findings are important in that they suggest that increases in venous pressure during acute hypertension are sufficient to account for disruption of the BBB. Intracarotid or topical application of hyperosmolar solutions disrupt the BBB primarily in venules. 38 We examined the possibility that increases in pial venous pressure during hyperosmolar solutions may contribute to disruption of the BBB in venules. Hyperosmolar arabinose, however, did not increase pial venous pressure. This finding provides further evidence for the concept that the mechanism of disruption of the BBB is different during hyperosmolar solutions and during acute hypertension.3 Disruption of the BBB during acute hypertension and superior venae cavae occlusion could be a transient response to increases in venous pressure, with increases in permeability that parallel increases in cerebral venous pressure, or a more prolonged effect which persists after venous pressure returns to normal. Data obtained 40 minutes following acute hypertension and superior venae cavae occlusion indicate that the BBB remains disrupted even though venous pressure was no longer elevated. It is possible that acute hypertension may initiate a prolonged, continued stimulus to disruption. This concept is supported by findings indicating that inhibitors of cyclooxygenase and free radicals reduce cerebral vascular damage produced by acute hypertension." Kontos12 also has shown that production of free radicals during acute hypertension continues for at least 1 hour after pressure returns to normal. If disruption of the BBB during acute hypertension is mediated by oxygen radicals, our finding that disruption persists after venous pressure returns to normal is.
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Seminiferous tubules were dissected in a petri dish containing PBS under a transillumination microscope and segments -1 mm ; were transferred in 15 ~1 medium onto a microscope slide. They were carefully squashed under a coverslip, and the stage of the cycle 17 ; was identified under a phase contrast microscope 18 ; . Slides were frozen in liquid N the coverslip was removed, and slides were briefly dipped in ice-cold ethanol. Slides were fixed for 10 min in 10% formalin and.
Genus BULLALVEOLINA F i r and Last, Tert L M. Olig: B. bulloides, Gaas beds M. Olig ; , France Reichel 1937 ; . Genus PRAEALVEOLINA S.S. ; First, Cret Cenom: P. cretacea, "Cenomanian" strata, France Reichel 1937 ; . Last, Cret Turon: P. cretaeea brevis, "Turonian" strata, France, Reichel 1937 ; . C o The record ofP. sp. by Owen & Nasr 1958 ; , Senonian, Iraq, is not believed to be authentic. The U. Alb age given by Reichel, in Treatise C, is dependent upon opinion as to where to place the Alb Cenom boundary. Subgenus PRAEALVEOLINA SIMPLALVEOLINA ; F i r and Last, Cret Cenom: P. S. ; simplex, "Cenomanian" strata, France Reichel 1937 ; . Genus OVALVEOLINA F i r Cret Cenom: O. ovum, "Cenomanian" strata, France Reichel 1937 ; . Last, Cret Turon: O. ovum, "Turonian" strata, France Reichel 1937 ; . C o The U. Alb age given by Reichel, in Treatise C, is dependent upon opinion as to where to place the Alb Cenom boundary. Genus CISALVEOLINA First, Cret Cenom: C. fallax, "Cenomanian" 1st, U. Cenom ; , Iran Reichel 1941 ; . Last, Cret Turon: C.fallax, Mishrif fm L. Turonian ; , Iraq Owen & Nasr 1958 ; . Genus COSINELLA First, Cret Cenom: C. viaUii, "Cenomanian" strata, Italy Colalongo 1963 ; . Last, Cret Maestr: C. cardenasensis, Cardenas beds, Mexico Colalongo 1963 ; . Genus 8UBALVEOLINA F i r and Last, Cret Campan: S. dordonica, "Campanian" 1st, France Reichel 1937 ; . Genus MULTISPIRINA F i r Cret Cenom: M. iranensis, "Cenomanian" 1st, Iran Reichel 1947 ; . Last, Cret Turon: M. iranensis, Mishriffm, Iraq Owen & Nasr 1958 ; . Genus PSEUDEDOMIA First, Cret Cenom: P. drorimensis, Drorim fm, Israel Reiss, Hamaoui & Ecker 1964 ; . Last, Cret Maestr: P. multistriata, Aruma group, O atar Henson 1948a ; . Family ORBITOLINIDAE Genus ORBITOLINA The use of this generic name for a foraminifer is not strictly in accord with the Rules--see Treatise F ; . First, Cret Barrem: O. conulus, "U. Barremian" strata, France Douvill6 1912 ; . Last, Cret Cenom: O. concava, "Cenomanian" strata, Middle East Henson 1948a ; . C o The record of Orbitolina by Marie & Fadre 1960 ; , U. Jur, Spain, is very doubtful; they could be Orbitolinopsis of Valanginian age. The overlying beds called "Purbeckian" contain Natica cf. vilanovae, which is an Apt species. Genus ABRAm ; IA F i and Last, Cret Maestr: A. mosae, Maestricht chalk, Holland Hofker 1955 ; . 320.
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MARILYN E. MORRIS, HWA-JEONG LEE, AND LISA M. PREDKO Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, University at Buffalo, State University of New York, Amherst, New York.
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In comparison with the 5 mg day T dosing achieved with the TTD, the biweekly administration of 200 mg T enanthate corresponds to a calculated time-averaged dose of 10.3 mg of unesterified T per day. This calculated dose exceeds the daily T production of most healthy young men 3, 8 ; . Although the actual delivered dose of unesterified T varies daily during the IM dosing interval, the timeaveraged BT levels observed with the IM regimen were approximately 2-fold greater than the time-averaged BT levels for TTD Table 2 ; , consistent with the calculated and nominal daily doses of the corresponding regimens. Despite the different amounts of T delivered, both treatments maintained sexual function and mood at the prior treatment levels, as demonstrated by objective Rigiscan ; and subjective assessments during the study. These findings are consistent with those of the earlier study of TTD therapy in hypogonadal men 12 ; . It should be noted, however.
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